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US FluView - Weekly Surveillance Flu report 2023/2024 season - for trend analysis

Weekly U.S. Influenza Surveillance Report


Print
Updated March 15, 2024
fluview-banner2.jpg

Key Updates for Week 10, ending March 9, 2024

Seasonal influenza activity remains elevated nationally with increases in some parts of the country. Viruses


Clinical Lab 15.4%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2) and B viruses were reported in approximately equal proportions this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 3.7%

(Trend )


of visits to a health care provider this week were for respiratory illness
(above baseline).


Outpatient Respiratory Illness: Activity Map
This week 13 jurisdictions experienced moderate activity and 16 jurisdictions experienced high or very high activity.

FluSurv-NET 67.9 per 100,000


cumulative hospitalization rate.

NHSN Hospitalizations 8,819 (Trend )


patients admitted to hospitals with influenza this week.

NCHS Mortality 0.7%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 15


influenza-associated deaths were reported (2 occurred during 2022-2023 season and 13 occurred during 2023-2024 season).

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains elevated nationally with increases in some parts of the country.
  • Nationally, percent positivity for both influenza A and B increased compared to last week; however, trends in percent positivity for influenza A and B varied by region.
  • Nationally, outpatient respiratory illness declined but remains above baseline.[SUP]1 [/SUP]Region 9 is at their baseline during Week 10 for the first time since late October, while the remaining HHS regions remain above their respective baselines.
  • Nationally, the number of weekly flu hospital admissions has been decreasing since January.
  • During Week 10, of the 575 viruses reported by public health laboratories, 384 (66.8%) were influenza A and 191 (33.2%) were influenza B. Of the 258 influenza A viruses subtyped during Week 10, 141 (54.7%) were influenza A(H1N1)pdm09 and 117 (45.3%) were A(H3N2).
  • Thirteen influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 10, bringing the season total to 116 pediatric deaths.
  • CDC estimates that there have been at least 29 million illnesses, 320,000 hospitalizations, and 20,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as influenza viruses are spreading.[SUP]2[/SUP] Vaccination can still provide benefit this season.
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories increased (change of >0.5 percentage points) compared to the previous week, but trends varied by region. Regions 5 and 10 reported an increase; regions 2, 4, 6, 8, and 9 reported a decrease; and regions 1, 3, and 7 remained stable during Week 10 compared to Week 9. The regions with the highest percent positivity were regions 7 (28.1%), 5 (22.3%), and 3 (17.0%). Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses circulated at approximately equal proportions during Week 10. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Viruses known to be associated with recent receipt of live attenuated influenza vaccine (LAIV) or found upon further testing to be a vaccine virus are not included, as they are not circulating influenza viruses. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested65,8092,419,084
No. of positive specimens (%)10,161 (15.4%)279,439 (11.6%)
Positive specimens by type
Influenza A5,532 (54.4%)203,348 (72.8%)
Influenza B4,629 (45.6%)76,081 (27.2%)
6

INFLUENZA Virus Isolated
View Chart Data | View Full Screen Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested2,30787,432
No. of positive specimens57528,235
Positive specimens by type/subtype
Influenza A384 (66.8%)22,468 (79.6%)
Subtyping Performed258 (67.2%)18,378 (81.8%)
(H1N1)pdm09141 (54.7%)13,557 (73.8%)
H3N2117 (45.3%)4,821 (26.2%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed126 (32.8%)4,090 (18.2%)
Influenza B191 (33.2%)5,767 (20.4%)
Lineage testing performed147 (77.0%)4,874 (84.5%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage147 (100.0%)4,874 (100.0%)
Lineage not performed44 (23.0%)893 (15.5%)
INFLUENZA Virus Isolated
View Chart Data | View Full Screen
Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 2,640 influenza viruses collected since October 1, 2023.
A/H11,148
6B.1A.5a1,148 (100%)2a285 (24.8%)
2a.1863 (75.2%)
A/H3777
3C.2a1b.2a777 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.1774 (99.6%)
2b1 (0.1%)
B/Victoria715
V1A715 (100%)3a.2715 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 172 A(H1N1)pdm09 viruses were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 192 A(H3N2) viruses were antigenically characterized by HI or HINT, and 190 (99.0%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 106 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 01, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested2,5941,128778688
Reduced Inhibition1 (0.4%)1 (0.1%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition1 (0.4%)1 (0.1%)0 (0.0%)0 (0.0%)
PeramivirViruses Tested2,5941,128778688
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition1 (0.4%)1 (0.1%)0 (0.0%)0 (0.0%)
ZanamivirViruses Tested2,5941,128778688
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested2,5181,098759661
Decreased Susceptibility1 (0.4%)0 (0.0%)1 (0.1%)0 (0.0%)
One A(H1N1)pdm09 virus had NA-H275Y amino acid substitution and showed highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir.

One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationwide, during Week 10, 3.7% of patient visits reported through ILINet were due to respiratory illness that included fever plus a cough or sore throat, also referred to as ILI. This has decreased (change of >0.1 percentage points) compared to Week 9 and remains above the national baseline. The percentage of visits for ILI increased in regions 8 and 10 and decreased in all other regions (1, 2, 3, 4, 5, 6, 7, and 9) compared to Week 9. Region 9 is at their baseline, while all other regions remain above their region-specific baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

national levels of ILI and ARI
* Effective October 3, 2021 (week 40), the ILI definition (fever plus cough or sore throat) no longer includes “without a known cause other than influenza.”

View Chart Data (current season only) | View Full Screen Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in 4 age groups (0-4 years, 5-24 years, 25-49 years, and 50-64 years), and remained stable in the 65+ years age group during Week 10 compared to Week 9.

national levels of ILI and ARI by age group
View Chart Data | View Full Screen Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 10
(Week ending
Mar. 9, 2024)
Week 9
(Week ending
Mar. 2, 2024)
Week 10
(Week ending
Mar. 9, 2024)
Week 9
(Week ending
Mar. 2, 2024)
Very High351116
High13175892
Moderate131595102
Low179203200
Minimal99337299
Insufficient Data00225220




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 20,741 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and March 9, 2024. The weekly hospitalization rate observed in Week 10 was 2.1 per 100,000 population. The weekly hospitalization rate observed during Week 52 is the third highest peak weekly rate observed during all seasons going back to 2010-2011 following the 2014-2015 and 2017-2018 seasons. The overall cumulative hospitalization rate was 67.9 per 100,000 population. This cumulative hospitalization rate is the second highest cumulative hospitalization rate when compared against previous end-of-season rates for Week 10, and it is the second highest cumulative in-season hospitalization rate observed in Week 10, following the 2017-2018 season (89.9). Cumulative in-season hospitalization rates observed in Week 10 from 2010-2011 through 2022-2023 ranged from 0.7 to 61.6.

When examining rates by age, the highest cumulative hospitalization rate per 100,000 population was among adults aged 65 years and older (184.3), followed by adults aged 50-64 years (81.5) and children aged 0-4 years (71.1). When examining age-adjusted rates by race and ethnicity, the highest rate of hospitalization per 100,000 population was among non-Hispanic Black persons (128.9), followed by non-Hispanic American Indian or Alaska Native persons (94.9), Hispanic persons (64.2), non-Hispanic White persons (51.9), and non-Hispanic Asian/Pacific Islander persons (36.1).

Among 20,741 hospitalizations, 17,868 (86.1%) were associated with influenza A virus, 2,745 (13.2%) with influenza B virus, 41 (0.2%) with influenza A virus and influenza B virus co-infection, and 87 (0.4%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 2,997 (72.4%) were A(H1N1) pdm09 and 1,138 (27.5%) were A(H3N2).

Among 2,315 hospitalized adults with information on underlying medical conditions, 95.6% had at least one reported underlying medical condition, the most commonly reported were hypertension, cardiovascular disease, obesity, and metabolic disease. Among 1,193 hospitalized women of childbearing age (15-49 years) with information on pregnancy status, 23.2% were pregnant. Among 675 hospitalized children with information on underlying medical conditions, 69.5% had at least one reported underlying medical condition; the most commonly reported was asthma, followed by obesity and neurologic disease.

FluSurvNet Cumulative Rates

View Full Screen

In this figure, cumulative rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospitals admissions are subject to reporting delays. As hospitalization data are reviewed each week, prior case counts and rates are updated accordingly.

FluSurvNet Weekly Rate

View Full Screen

In this figure, weekly rates for all seasons prior to the 2023-24 season reflect end-of-season rates. For the 2023-24 season, rates for recent hospital admissions are subject to reporting delays and are shown as a dashed line for the current season. As hospitalization data are received each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Hospitals report to NHSN the weekly number of patients admitted with laboratory-confirmed influenza. During Week 10, 8,819 patients with laboratory-confirmed influenza were admitted to a hospital. Nationally and in all HHS regions, the number of patients admitted to a hospital with laboratory-confirmed influenza for Week 10 decreased (change of >5%) compared to Week 9.

Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on March 14, 2024, 0.7% of the deaths that occurred during the week ending March 9, 2024 (Week 10) were due to influenza. This percentage increased (≥ 0.1 percentage point change) compared to Week 9. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Fifteen influenza-associated pediatric deaths were reported to CDC during Week 10.

Thirteen deaths occurred during the 2023-2024 season, bringing the total pediatric deaths for this season to 116. The deaths occurred during Week 52 of 2023 (the week ending December 30, 2023) and between weeks 4 and 9 of 2024 (the weeks ending January 27, 2024, and March 2, 2024). Nine deaths were associated with influenza A viruses. Six of the influenza A viruses had subtyping performed; five were A(H1N1) viruses and one was an A(H3) virus. Three deaths were associated with influenza B viruses with no lineage determined. One death was associated with a co-infection with influenza A(H1N1) and influenza B viruses.

Two deaths occurring during the 2022-2023 season were also reported, which brings the total number of pediatric deaths for last season to 184. One death was associated with an influenza A(H3) virus and occurred during Week 47 of 2022 (the week ending November 26, 2022). The other death was associated with an influenza A(H1N1) virus and occurred during Week 1 of 2023 (the week ending January 7, 2023).

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated March 22, 2024
fluview-banner2.jpg

Key Updates for Week 11, ending March 16, 2024

Seasonal influenza activity remains elevated nationally but is decreasing. Activity is decreasing or stable in nine HHS regions and increasing slightly in the Pacific Northwest. Viruses


Clinical Lab 12.0%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 3.4%

(Trend )


of visits to a health care provider this week were for respiratory illness
(above baseline).


Outpatient Respiratory Illness: Activity Map
This week 13 jurisdictions experienced moderate activity and 9 jurisdictions experienced high or very high activity.

FluSurv-NET 70.2 per 100,000


cumulative hospitalization rate.

NHSN Hospitalizations 6,973 (Trend )


patients admitted to hospitals with influenza this week.

NCHS Mortality 0.6%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 5


influenza-associated deaths were reported this week for a total of 121 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains elevated but is decreasing nationally. Activity is decreasing or stable in nine of the 10 HHS regions; however, the Pacific Northwest reported a slight increase this week.
  • Nationally, percent positivity for both influenza A and B decreased compared to last week.
  • Nationally, outpatient respiratory illness declined but remains above baseline.[SUP]1 [/SUP]Region 2 is below their baseline, while all other HHS regions remain at or above their region-specific baselines.
  • Nationally, the number of weekly flu hospital admissions has been decreasing since January.
  • During Week 11, of the 426 viruses reported by public health laboratories, 275 (64.6%) were influenza A and 151 (35.4%) were influenza B. Of the 198 influenza A viruses subtyped during Week 11, 87 (43.9%) were influenza A(H1N1)pdm09 and 111 (56.1%) were A(H3N2).
  • Five influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 11, bringing the season total to 121 pediatric deaths.
  • CDC estimates that there have been at least 30 million illnesses, 340,000 hospitalizations, and 21,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as influenza viruses are spreading.[SUP]2[/SUP] Vaccination can still provide benefit this season.
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories decreased (change of >0.5 percentage points) compared to the previous week. Region 10 reported an increase; regions 1, 2, 3, 4, 5, 6, and 7 reported a decrease; and regions 8 and 9 remained stable during Week 11 compared to Week 10. The regions with the highest percent positivity were regions 7 (24.5%), 5 (18.9%), and 8 (12.4%). Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Viruses known to be associated with recent receipt of live attenuated influenza vaccine (LAIV) or found upon further testing to be a vaccine virus are not included, as they are not circulating influenza viruses. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested82,2022,577,255
No. of positive specimens (%)9,862 (12.0%)299,652 (11.6%)
Positive specimens by type
Influenza A5,121 (51.9%)214,693 (71.6%)
Influenza B4,741 (48.1%)84,949 (28.4%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested2,01290,420
No. of positive specimens42629,239
Positive specimens by type/subtype
Influenza A275 (64.6%)23,120 (79.1%)
Subtyping Performed198 (72.0%)19,010 (82.2%)
(H1N1)pdm0987 (43.9%)13,853 (72.9%)
H3N2111 (56.1%)5,157 (27.1%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed77 (28.0%)4,110 (17.8%)
Influenza B151 (35.4%)6,119 (20.9%)
Lineage testing performed118 (78.1%)5,196 (84.9%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage118 (100.0%)5,196 (100.0%)
Lineage not performed33 (21.9%)923 (15.1%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 2,816 influenza viruses collected since October 1, 2023.
A/H11,200
6B.1A.5a1,200 (100%)2a293 (24.4%)
2a.1907 (75.6%)
A/H3842
3C.2a1b.2a842 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.1839 (99.6%)
2b1 (0.1%)
B/Victoria774
V1A774 (100%)3a.2774 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 200 A(H1N1)pdm09 viruses were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 192 A(H3N2) viruses were antigenically characterized by HI or HINT, and 190 (99.0%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 127 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 01, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested2,8121,202840770
Reduced Inhibition1 (0.04%)1 (0.1%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition1 (0.04%)1 (0.1%)0 (0.0%)0 (0.0%)
PeramivirViruses Tested2,8121,202840770
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition1 (0.04%)1 (0.1%)0 (0.0%)0 (0.0%)
ZanamivirViruses Tested2,8121,202840770
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested2,7371,171823743
Decreased Susceptibility1 (0.04%)0 (0.0%)1 (0.1%)0 (0.0%)
One A(H1N1)pdm09 virus had NA-H275Y amino acid substitution and showed highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir.

One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationwide, during Week 11, 3.4% of patient visits reported through ILINet were due to respiratory illness that included fever plus a cough or sore throat, also referred to as ILI. This has decreased (change of >0.1 percentage points) compared to Week 10 and remains above the national baseline. The percentage of visits for ILI decreased in regions 1, 2, 3, 4, 5, 6, and 7 and remained stable in regions 8, 9, and 10 compared to Week 10. Region 2 is below its baseline, regions 4, 8, and 9 are at their respective baselines, and the remaining regions are above their respective baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in all age groups in Week 11 compared to Week 10.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 11
(Week ending
Mar. 16, 2024)
Week 10
(Week ending
Mar. 9, 2024)
Week 11
(Week ending
Mar. 16, 2024)
Week 10
(Week ending
Mar. 9, 2024)
Very High23411
High7144260
Moderate13126994
Low2016194200
Minimal1210377345
Insufficient Data10243219




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 21,443 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and March 16, 2024. The weekly hospitalization rate observed in Week 11 was 1.7 per 100,000 population. The weekly hospitalization rate observed during Week 52 is the third highest peak weekly rate observed during all seasons going back to 2010-2011 following the 2014-2015 and 2017-2018 seasons. The overall cumulative hospitalization rate was 70.2 per 100,000 population. This cumulative hospitalization rate is the second highest cumulative hospitalization rate when compared against previous end-of-season rates for Week 11, and it is the second highest cumulative in-season hospitalization rate observed in Week 11, following the 2017-2018 season (93.5). Cumulative in-season hospitalization rates observed in Week 11 from 2010-2011 through 2022-2023 ranged from 0.7 to 65.1.

When examining rates by age, the highest cumulative hospitalization rate per 100,000 population was among adults aged 65 years and older (191.0), followed by adults aged 50-64 years (83.8) and children aged 0-4 years (73.8). When examining age-adjusted rates by race and ethnicity, the highest rate of hospitalization per 100,000 population was among non-Hispanic Black persons (132.2), followed by non-Hispanic American Indian or Alaska Native persons (97.2), Hispanic persons (65.7), non-Hispanic White persons (53.9), and non-Hispanic Asian/Pacific Islander persons (37.0).

Among 21,443 hospitalizations, 18,406 (85.8%) were associated with influenza A virus, 2,888 (13.5%) with influenza B virus, 49 (0.2%) with influenza A virus and influenza B virus co-infection, and 100 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,081 (72.3%) were A(H1N1) pdm09 and 1,181 (27.7%) were A(H3N2).

Among 2,491 hospitalized adults with information on underlying medical conditions, 95.5% had at least one reported underlying medical condition, the most commonly reported were hypertension, cardiovascular disease, obesity, and metabolic disease. Among 1,234 hospitalized women of childbearing age (15-49 years) with information on pregnancy status, 22.9% were pregnant. Among 736 hospitalized children with information on underlying medical conditions, 69.9% had at least one reported underlying medical condition; the most commonly reported was asthma, followed by obesity and neurologic disease.



In this figure, cumulative and weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospitals admissions are subject to reporting delays. As hospitalization data are reviewed each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Hospitals report to NHSN the weekly number of patients admitted with laboratory-confirmed influenza. During Week 11, 6,973 patients with laboratory-confirmed influenza were admitted to a hospital. Nationally and in regions 1, 2, 3, 4, 5, 6, and 7, the number of patients admitted to a hospital with laboratory-confirmed influenza for Week 11 decreased (change of >5%) compared to Week 10. The number of hospitalizations with laboratory-confirmed influenza increased in regions 8 and 10 and remained stable in Region 9.

Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on March 21, 2024, 0.6% of the deaths that occurred during the week ending March 16, 2024 (Week 11), were due to influenza. This percentage decreased (≥ 0.1 percentage point change) compared to Week 10. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Five influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 11. The deaths occurred during weeks 2, 9, and 11 of 2024 (the weeks ending January 13, March 2, and March 16, respectively). Two deaths were associated with influenza A(H1N1) viruses and three deaths were associated with influenza B viruses with no lineage determined.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated March 29, 2024
fluview-banner2.jpg

Key Updates for Week 12, ending March 23, 2024

Seasonal influenza activity remains elevated nationally but is decreasing. Viruses


Clinical Lab 10.5%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 3.1%

(Trend )


of visits to a health care provider this week were for respiratory illness
(above baseline).


Outpatient Respiratory Illness: Activity Map
This week 4 jurisdictions experienced moderate activity and 9 jurisdictions experienced high activity.

FluSurv-NET 72.2 per 100,000


cumulative hospitalization rate.

NHSN Hospitalizations 5,738 (Trend )


patients admitted to hospitals with influenza this week.

NCHS Mortality 0.5%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 5


influenza-associated deaths were reported this week for a total of 126 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains elevated but is decreasing nationally.
  • Nationally, percent positivity for both influenza A and B decreased compared to last week.
  • One human infection with an influenza A(H1N2) variant virus was reported by the Pennsylvania Department of Health.
  • Nationally, outpatient respiratory illness declined but remains above baseline.[SUP]1 [/SUP]Regions 2, 4, 6, and 8 are below their baselines, while all other HHS regions remain at or above their region-specific baselines.
  • Nationally, the number of weekly flu hospital admissions has been decreasing since January.
  • During Week 12, of the 403 viruses reported by public health laboratories, 239 (59.3%) were influenza A and 164 (40.7%) were influenza B. Of the 172 influenza A viruses subtyped during Week 12, 76 (44.2%) were influenza A(H1N1)pdm09 and 96 (55.8%) were A(H3N2).
  • Five influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 11, bringing the season total to 126 pediatric deaths.
  • CDC estimates that there have been at least 31 million illnesses, 350,000 hospitalizations, and 22,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as influenza viruses are spreading.[SUP]2[/SUP] Vaccination can still provide benefit this season.
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories decreased (change of >0.5 percentage points) compared to the previous week. Regions 3, 5, 6, 7, 8, and 10 reported a decrease; regions 1, 4, and 9 remained stable; and region 2 reported an increase (likely a reporting artifact) during Week 12 compared to Week 11. The regions with the highest percent positivity were regions 7 (20.1%), 5 (16.4%), and 1 (10.4%). Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Viruses known to be associated with recent receipt of live attenuated influenza vaccine (LAIV) or found upon further testing to be a vaccine virus are not included, as they are not circulating influenza viruses. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested77,1832,663,679
No. of positive specimens (%)8,088 (10.5%)311,936 (11.7%)
Positive specimens by type
Influenza A4,130 (51.1%)220,085 (70.6%)
Influenza B3,958 (48.9%)91,841 (29.4%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested1,91793,464
No. of positive specimens40330,309
Positive specimens by type/subtype
Influenza A239 (59.3%)23,805 (78.5%)
Subtyping Performed172 (72.0%)19,659 (82.6%)
(H1N1)pdm0976 (44.2%)14,150 (72.0%)
H3N296 (55.8%)5,509 (28.0%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed67 (28.0%)4,146 (17.4%)
Influenza B164 (40.7%)6,504 (21.5%)
Lineage testing performed116 (70.7%)5,517 (84.8%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage116 (100.0%)5,517 (100.0%)
Lineage not performed48 (29.3%)987 (15.2%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Novel Influenza A Virus:


A human infection with a novel influenza A virus was reported by the Pennsylvania Department of Health. The patient was infected with an influenza A(H1N2) variant (A(H1N2)v) virus. The patient is < 18 years of age, sought healthcare during the week ending March 9, 2024 (week 10), was hospitalized, and has since recovered. An investigation by local public health officials found that the patient had swine contact prior to their illness onset. Additional investigation identified mild illness in two of the patient’s close contacts who also had contact with swine, that began prior to the patient’s onset of symptoms. No person-to-person transmission of A(H1N2)v virus associated with this patient has been identified. The investigation is ongoing. This is the first human infection with a variant influenza A virus reported in the United States in 2024.

When an influenza virus that normally circulates in swine (but not people) is detected in a person, it is called a “variant” influenza virus. Most human infections with variant influenza viruses occur following exposure to swine, but human-to-human transmission can occur. It is important to note that in most cases, variant influenza viruses have not shown the ability to spread easily and sustainably from person to person.

Early identification and investigation of human infections with novel influenza A viruses are critical so that the risk of infection can be understood, and appropriate public health measures can be taken.

Additional information on influenza in swine, variant influenza virus infection in humans, and guidance to interact safely with swine can be found at www.cdc.gov/flu/swineflu/index.htm.

Additional information regarding human infections with novel influenza A viruses:

Surveillance Methods | FluView Interactive Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 3,211 influenza viruses collected since October 1, 2023.
A/H11,342
6B.1A.5a1,342 (100%)2a331 (24.7%)
2a.11,011 (75.3%)
A/H3989
3C.2a1b.2a989 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.1986 (99.7%)
2b1 (0.1%)
B/Victoria880
V1A880 (100%)3a.2880 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 200 A(H1N1)pdm09 viruses were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 223 A(H3N2) viruses were antigenically characterized by HI or HINT, and 221 (99.1%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 149 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 01, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested3,1061,314937855
Reduced Inhibition1 (0.03%)1 (0.1%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition2 (0.1%)2 (0.2%)0 (0.0%)0 (0.0%)
PeramivirViruses Tested3,1061,314937855
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition2 (0.1%)2 (0.2%)0 (0.0%)0 (0.0%)
ZanamivirViruses Tested3,1061,314937855
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested3,0181,275915828
Decreased Susceptibility1 (0.05%)0 (0.0%)1 (0.1%)0 (0.0%)
Two A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution and showed highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, during Week 12, 3.1% of patient visits reported through ILINet were due to respiratory illness that included fever plus a cough or sore throat, also referred to as ILI. This has decreased (change of >0.1 percentage points) for the fourth consecutive week but remains above the national baseline. The percentage of visits for ILI remained stable in regions 2 and 9 and decreased in all other regions in Week 12 compared to Week 11. Regions 2, 4, 6 and 8 are below their baseline, and regions 1, 3, 5, 7, 9, and 10 are at or above their respective baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years, 5-24 years, and 25-49 years age groups, and remained stable in the 50-64 years and 65+ years age groups in Week 12 compared to Week 11.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 12
(Week ending
Mar. 23, 2024)
Week 11
(Week ending
Mar. 16, 2024)
Week 12
(Week ending
Mar. 23, 2024)
Week 11
(Week ending
Mar. 16, 2024)
Very High0124
High992544
Moderate4125372
Low2019158188
Minimal2214463393
Insufficient Data00228228




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 22,080 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and March 23, 2024. The weekly hospitalization rate observed in Week 12 was 1.4 per 100,000 population. The peak weekly hospitalization rate was observed during Week 52 and is the third highest peak weekly rate observed during all seasons going back to 2010-2011 following the 2014-2015 and 2017-2018 seasons. The overall cumulative hospitalization rate for the season was 72.2 per 100,000 population. This cumulative hospitalization rate is the second highest cumulative hospitalization rate when compared against previous end-of-season rates for Week 12, and it is the second highest cumulative in-season hospitalization rate observed in Week 12, following the 2017-2018 season (96.1). Cumulative in-season hospitalization rates observed in Week 12 from 2010-2011 through 2022-2023 ranged from 0.7 to 67.3.

When examining rates by age, the highest cumulative hospitalization rate per 100,000 population was among adults aged 65 years and older (196.9), followed by adults aged 50-64 years (86.1) and children aged 0-4 years (75.3). When examining age-adjusted rates by race and ethnicity, the highest rate of hospitalization per 100,000 population was among non-Hispanic Black persons (135.0), followed by non-Hispanic American Indian or Alaska Native persons (101.5), Hispanic persons (65.6), non-Hispanic White persons (55.6), and non-Hispanic Asian/Pacific Islander persons (37.8).

Among 22,080 hospitalizations, 18,898 (85.6%) were associated with influenza A virus, 3,028 (13.7%) with influenza B virus, 45 (0.2%) with influenza A virus and influenza B virus co-infection, and 109 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,173 (71.5%) were A(H1N1) pdm09 and 1,258 (28.4%) were A(H3N2).

Among 2,638 hospitalized adults with information on underlying medical conditions, 95.4% had at least one reported underlying medical condition, the most commonly reported were hypertension, cardiovascular disease, obesity, and metabolic disease. Among 1,276 hospitalized women of childbearing age (15-49 years) with information on pregnancy status, 22.6% were pregnant. Among 810 hospitalized children with information on underlying medical conditions, 69.0% had at least one reported underlying medical condition; the most commonly reported was asthma, followed by obesity and neurologic disease.



In these figures, cumulative and weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospitals admissions are subject to reporting delays. As hospitalization data are reviewed each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Hospitals report to NHSN the weekly number of patients admitted with laboratory-confirmed influenza. During Week 12, 5,738 patients with laboratory-confirmed influenza were admitted to a hospital. Nationally and in regions 1, 2, 3, 4, 5, 6, 7, 8, and 9, the number of patients admitted to a hospital with laboratory-confirmed influenza for Week 12 decreased (change of >5%) compared to Week 11. The number of hospitalizations with laboratory-confirmed influenza increased slightly in region 10.

Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on March 28, 2024, 0.5% of the deaths that occurred during the week ending March 23, 2024 (Week 12), were due to influenza. This percentage remained stable (< 0.1 percentage point change) compared to Week 11. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Five influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 12. The deaths occurred during week 52 of 2023 (the week ending December 30, 2023) and during weeks 2 and 10 of 2024 (the weeks ending January 13, 2024, and March 9, 2024). Three deaths were associated with influenza A viruses and two deaths were associated with influenza B viruses. Two of the influenza A viruses had subtyping performed; one was an A(H1N1) virus and one was an A(H3) virus. Neither of the influenza B viruses had lineage determined.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated April 5, 2024
fluview-banner2.jpg

Key Updates for Week 13, ending March 30, 2024

Seasonal influenza activity remains elevated nationally but is decreasing. Viruses


Clinical Lab 9.1%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 3.0%

(Trend )


of visits to a health care provider this week were for respiratory illness
(above baseline).


Outpatient Respiratory Illness: Activity Map
This week 5 jurisdictions experienced moderate activity and 6 jurisdictions experienced high activity.

FluSurv-NET 74.2 per 100,000


cumulative hospitalization rate.

NHSN Hospitalizations 5,299 (Trend )


patients admitted to hospitals with influenza this week.

NCHS Mortality 0.5%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 7


influenza-associated deaths were reported this week for a total of 133 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains elevated but is decreasing nationally.
  • Nationally, percent positivity for both influenza A and B decreased compared to last week.
  • One human infection with a highly pathogenic avian influenza (HPAI) A(H5N1) virus was reported by the Texas Department of Health.
  • Nationally, outpatient respiratory illness declined but remains above baseline.[SUP]1 [/SUP]Regions 2, 4, 6, 8, 9, and 10 are below their baselines, while all other HHS regions remain at or above their region-specific baselines.
  • Nationally, the number of weekly flu hospital admissions has been decreasing since January.
  • During Week 13, of the 329 viruses reported by public health laboratories, 201 (61.1%) were influenza A and 128 (38.9%) were influenza B. Of the 138 influenza A viruses subtyped during Week 13, 69 (50.0%) were influenza A(H1N1)pdm09 and 69 (50.0%) were A(H3N2).
  • Seven influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 13, bringing the season total to 133 pediatric deaths.
  • CDC estimates that there have been at least 32 million illnesses, 360,000 hospitalizations, and 22,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as influenza viruses are spreading.[SUP]2[/SUP] Vaccination can still provide benefit this season.
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories decreased (change of >0.5 percentage points) compared to the previous week. Regions 1, 3, 4, 5, 6, 8, 9, and 10 decreased in percent positivity; region 7 remained stable, and region 2 reported an increase during Week 13 compared to Week 12. The regions with the highest percent positivity were regions 7 (19.1%), 5 (14.0%), and 2 (10.8%). Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Viruses known to be associated with recent receipt of live attenuated influenza vaccine (LAIV) or found upon further testing to be a vaccine virus are not included, as they are not circulating influenza viruses. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested68,9892,773,210
No. of positive specimens (%)6,293 (9.1%)320,162 (11.5%)
Positive specimens by type
Influenza A3,081 (49.0%)224,430 (70.1%)
Influenza B3,212 (51.0%)95,722 (29.9%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested1,78596,345
No. of positive specimens32931,394
Positive specimens by type/subtype
Influenza A201 (61.1%)24,500 (78%)
Subtyping Performed138 (68.7%)20,284 (82.8%)
(H1N1)pdm0969 (50%)14,449 (71.2%)
H3N269 (50%)5,835 (28.8%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed63 (31.3%)4,216 (17.2%)
Influenza B128 (38.9%)6,894 (22%)
Lineage testing performed86 (67.2%)5,854 (84.9%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage86 (100.0%)5,854 (100.0%)
Lineage not performed42 (32.8%)1,040 (15.1%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Novel Influenza A Virus:


A human infection with highly pathogenic avian influenza (HPAI) A(H5N1) virus was reported by the Texas Department of State Health Services and confirmed by CDC on March 30, 2024.

A patient aged >18 years in Texas developed conjunctivitis on approximately March 27, 2024, while working at a commercial dairy cattle farm. HPAI A(H5N1) virus has been recently detected in dairy cattle, poultry and wild birds in Texas. Respiratory and conjunctival specimens were collected on March 28, 2024, and tested at the Texas Tech University Bioterrorism Response Laboratory that same day. RT-PCR analysis indicated that both specimens were presumptive positive for influenza A(H5) virus. The specimens were then sent to CDC for further testing. They were received and tested at CDC on March 30, 2024, and confirmed as HPAI A(H5N1) virus clade 2.3.4.4b using diagnostic RT-PCR and sequencing. The patient did not report symptoms other than conjunctivitis, was not hospitalized, and is recovering. Starting on March 29, 2024, the patient was recommended to isolate and was provided with influenza antivirals per CDC guidance (https://www.cdc.gov/flu/avianflu/clinicians-evaluating-patients.htm).

Public health officials are conducting surveillance activities in the area in response to this detection. Household contacts of the patient have not reported illness and have been provided influenza antiviral prophylaxis in accordance with CDC recommendations. No additional cases of human infection with HPAI A(H5N1) associated with this case and no human-to-human transmission of HPAI A(H5N1) virus have been identified.

This is the second person to test positive for HPAI A(H5N1) virus in the United States. The first was reported in April 2022 in Colorado.

Currently in the United States, HPAI A(H5N1) virus detections among wild birds are widespread, there are sporadic outbreaks among poultry and backyard flocks, and sporadic infections in wild mammals have been reported by United States Department of Agriculture (USDA) Animal Plant Health Inspection Service (APHIS). On March 25, USDA reported the first detections of H5N1 in dairy cattle in Texas and Kansas. Since then, additional detections in dairy cattle have been reported from Idaho, Michigan, New Mexico, and Ohio. USDA is continuing to monitor and test samples collected from other farms where cattle are displaying similar symptoms.

CDC recommends that state and local public health departments monitor people who were exposed to birds or other animals (including livestock) suspected to be infected with avian influenza viruses for onset of signs and symptoms until 10 days after their last exposure and that people who develop signs or symptoms of respiratory illness and/or conjunctivitis be tested for influenza. During February 9, 2022 — March 29, 2024, over 8,000 people were actively monitored following HPAI exposure.

Information about avian influenza is available at https://www.cdc.gov/flu/avianflu/index.htm.

Interim recommendations for Prevention, Monitoring, and Public Health Investigations are available at https://www.cdc.gov/flu/avianflu/hpai/hpai-interim-recommendations.html.

The latest case reports on avian influenza outbreaks in wild birds, commercial poultry; backyard or hobbyist flocks; and mammals in the United States are available from the USDA at https://www.aphis.usda.gov/aphis/ou...e-information/avian/avian-influenza/2022-hpai.

Additional information regarding human infections with novel influenza A viruses:

Surveillance Methods | FluView Interactive Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 3,263 influenza viruses collected since October 1, 2023.
A/H11,357
6B.1A.5a1,357 (100%)2a333 (24.5%)
2a.11,024 (75.5%)
A/H31,011
3C.2a1b.2a1,011 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,008 (99.7%)
2b1 (0.1%)
B/Victoria895
V1A895 (100%)3a.2895 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 217 A(H1N1)pdm09 viruses were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 249 A(H3N2) viruses were antigenically characterized by HI or HINT, and 246 (99%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 180 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 01, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested3,2551,3581,008889
Reduced Inhibition1 (0.03%)1 (0.07%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition2 (0.06%)2 (0.1%)0 (0.0%)0 (0.0%)
PeramivirViruses Tested3,2551,3581,008889
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition2 (0.06%)2 (0.1%)0 (0.0%)0 (0.0%)
ZanamivirViruses Tested3,2551,3581,008889
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested3,1631,319982862
Decreased Susceptibility1 (0.03%)0 (0.0%)1 (0.1%)0 (0.0%)
Two A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution and showed highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, during Week 13, 3.0% of patient visits reported through ILINet were due to respiratory illness that included fever plus a cough or sore throat, also referred to as ILI. This has remained stable (change of ≤ 0.1 percentage points) since Week 12 and remains above the national baseline. The percentage of visits for ILI decreased in regions 2, 3, 8, and 10, and remained stable in all other regions in Week 13 compared to Week 12. Regions 1, 3, 5, and 7 are at or above their baseline, and all other regions are below their respective baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years and 5-24 years age groups, and remained stable in the 25-49 years, 50-64 years, and the 65+ years age groups in Week 13 compared to Week 12.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 13
(Week ending
Mar. 30, 2024)
Week 12
(Week ending
Mar. 23, 2024)
Week 13
(Week ending
Mar. 30, 2024)
Week 12
(Week ending
Mar. 23, 2024)
Very High0012
High6102028
Moderate535352
Low2119138160
Minimal2323480466
Insufficient Data00237221




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 22,684 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and March 30, 2024. The weekly hospitalization rate observed in Week 13 was 1.3 per 100,000 population. The weekly hospitalization rate observed during Week 52 is the third highest peak weekly rate observed during all seasons going back to 2010-2011 following the 2014-2015 and 2017-2018 seasons. The overall cumulative hospitalization rate was 74.2 per 100,000 population. This cumulative hospitalization rate is the second highest cumulative hospitalization rate when compared against previous end-of-season rates for Week 13, and it is the second highest cumulative in-season hospitalization rate observed in Week 13, following the 2017-2018 season (99.9). Cumulative in-season hospitalization rates observed in Week 13 from 2010-2011 through 2022-2023 ranged from 0.7 to 67.9.

When examining rates by age, the highest cumulative hospitalization rate per 100,000 population was among adults aged 65 years and older (202.6), followed by adults aged 50-64 years (88.2) and children aged 0-4 years (76.5). When examining age-adjusted rates by race and ethnicity, the highest rate of hospitalization per 100,000 population was among non-Hispanic Black persons (138.4), followed by non-Hispanic American Indian or Alaska Native persons (102.7), Hispanic persons (69.3), non-Hispanic White persons (57.1), and non-Hispanic Asian/Pacific Islander persons (38.9).

Among 22,684 hospitalizations, 19,347 (85.3%) were associated with influenza A virus, 3,178 (14.0%) with influenza B virus, 43 (0.2%) with influenza A virus and influenza B virus co-infection, and 116 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,249 (71.5%) were A(H1N1) pdm09 and 1,298 (28.5%) were A(H3N2).

Among 2,758 hospitalized adults with information on underlying medical conditions, 95.3% had at least one reported underlying medical condition, the most commonly reported were hypertension, cardiovascular disease, obesity, and metabolic disease. Among 1,316 hospitalized women of childbearing age (15-49 years) with information on pregnancy status, 22.6% were pregnant. Among 853 hospitalized children with information on underlying medical conditions, 69.2% had at least one reported underlying medical condition; the most commonly reported was asthma, followed by obesity and neurologic disease.



In these figures, cumulative and weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospitals admissions are subject to reporting delays. As hospitalization data are reviewed each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Hospitals report to NHSN the weekly number of patients admitted with laboratory-confirmed influenza. During Week 13, 5,299 patients with laboratory-confirmed influenza were admitted to a hospital. Nationally and in regions 1, 3, 4, 5, 6, 8, 9, and 10, the number of patients admitted to a hospital with laboratory-confirmed influenza for Week 13 decreased (change of >5%) compared to Week 12. The number of hospitalizations with laboratory-confirmed influenza remained stable in regions 2 and 7.

Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on April 4, 2024, 0.5% of the deaths that occurred during the week ending March 30, 2024 (Week 13), were due to influenza. This percentage remained stable (< 0.1 percentage point change) compared to Week 12. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Seven influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 13. The deaths occurred during weeks 2, 6, 12 and 13 (the weeks ending January 13, February 10, March 23, and March 30 of 2024, respectively). Two deaths were associated with influenza A viruses. One of the influenza A viruses had subtyping performed and it was an A(H1N1) virus. Five deaths were associated with influenza B viruses. Two of the influenza B viruses had lineage determined and both were B/Victoria viruses.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated April 12, 2024
fluview-banner2.jpg

Key Updates for Week 14, ending April 6, 2024

Seasonal influenza activity remains elevated nationally but continues to decrease. Viruses


Clinical Lab 7.7%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 2.8%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Activity Map
This week 7 jurisdictions experienced moderate activity and 1 jurisdictions experienced high activity.

FluSurv-NET 76.0 per 100,000


cumulative hospitalization rate.

NHSN Hospitalizations 4,825 (Trend )


patients admitted to hospitals with influenza this week.

NCHS Mortality 0.4%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 5


influenza-associated deaths were reported this week for a total of 138 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains elevated but continues to decrease nationally.
  • Nationally, percent positivity for both influenza A and B decreased compared to last week.
  • Nationally, outpatient respiratory illness declined and is below baseline for the first time since late October.[SUP]1 [/SUP]Regions 2, 3, 4, 6, 8, 9, and 10 are below their baselines, while HHS regions 1, 5 and 7 remain above their region-specific baselines.
  • Nationally, the number of weekly flu hospital admissions has been decreasing since January.
  • During Week 14, of the 272 viruses reported by public health laboratories, 160 (58.8%) were influenza A and 112 (41.2%) were influenza B. Of the 104 influenza A viruses subtyped during Week 14, 45 (43.3%) were influenza A(H1N1)pdm09 and 59 (56.7%) were A(H3N2).
  • Five influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 14, bringing the season total to 138 pediatric deaths.
  • CDC estimates that there have been at least 33 million illnesses, 360,000 hospitalizations, and 23,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as influenza viruses are spreading.[SUP]2[/SUP] Vaccination can still provide benefit this season.
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories decreased (change of >0.5 percentage points) compared to the previous week. Regions 1, 2, 3, 5, 6, 8, and 10 decreased in percent positivity; regions 4 and 9 remained stable, and Region 7 reported a slight increase during Week 14 compared to Week 13. The regions with the highest percent positivity were regions 7 (17.6%), 5 (11.2%), and 1 (8.7%). Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Viruses known to be associated with recent receipt of live attenuated influenza vaccine (LAIV) or found upon further testing to be a vaccine virus are not included, as they are not circulating influenza viruses. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested66,1992,837,222
No. of positive specimens (%)5,111 (7.7%)327,063 (11.5%)
Positive specimens by type
Influenza A2,692 (52.7%)228,076 (69.7%)
Influenza B2,419 (47.3%)98,977 (30.3%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested1,11798,281
No. of positive specimens27232,302
Positive specimens by type/subtype
Influenza A160 (58.8%)24,958 (77.3%)
Subtyping Performed104 (65.0%)20,711 (83.0%)
(H1N1)pdm0945 (43.3%)14,652 (70.7%)
H3N259 (56.7%)6,059 (29.3%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed56 (35.0%)4,247 (17.0%)
Influenza B112 (41.2%)7,344 (22.7%)
Lineage testing performed69 (61.6%)6,140 (83.6%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage69 (100.0%)6,140 (100.0%)
Lineage not performed43 (38.4%)1,204 (16.4%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 3,369 influenza viruses collected since October 1, 2023.
A/H11,378
6B.1A.5a1,378 (100%)2a339 (24.6%)
2a.11,039 (75.4%)
A/H31,068
3C.2a1b.2a1,068 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,065 (99.7%)
2b1 (0.1%)
B/Victoria923
V1A923 (100%)3a.2923 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 217 A(H1N1)pdm09 viruses were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 249 A(H3N2) viruses were antigenically characterized by HI or HINT, and 246 (98.8%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 213 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 01, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested3,3501,3791,062909
Reduced Inhibition1 (0.03%)1 (0.07%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition2 (0.06%)2 (0.1%)0 (0.0%)0 (0.0%)
PeramivirViruses Tested3,3501,3791,062909
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition2 (0.06%)2 (0.1%)0 (0.0%)0 (0.0%)
ZanamivirViruses Tested3,3501,3791,062909
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested3,2611,3401,039882
Decreased Susceptibility1 (0.03%)0 (0.0%)1 (0.1%)0 (0.0%)
Two A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution and showed highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, during Week 14, 2.8% of patient visits reported through ILINet were due to respiratory illness that included fever plus a cough or sore throat, also referred to as ILI. This has decreased (change of ≥ 0.1 percentage points) since Week 13 and is now below the national baseline. The percentage of visits for ILI decreased in regions 2, 4, 5, 6, 7, and 8, and remained stable in all other regions in Week 14 compared to Week 13. Regions 1, 5, and 7 are above their baseline, and all other regions are below their respective baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years, 5-24 years, and 25-49 years age groups, and remained stable in the 50-64 years and 65+ years age groups in Week 14 compared to Week 13.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 14
(Week ending
Apr. 6, 2024)
Week 13
(Week ending
Mar. 30, 2024)
Week 14
(Week ending
Apr. 6, 2024)
Week 13
(Week ending
Mar. 30, 2024)
Very High0001
High161320
Moderate753753
Low1321127136
Minimal3323513495
Insufficient Data10239224




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 23,235 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and April 6, 2024. The weekly hospitalization rate observed in Week 14 was 1.2 per 100,000 population. The weekly hospitalization rate observed during Week 52 is the third highest peak weekly rate observed during all seasons going back to 2010-2011 following the 2014-2015 and 2017-2018 seasons. The overall cumulative hospitalization rate was 76.0 per 100,000 population. This cumulative hospitalization rate is the second highest cumulative hospitalization rate when compared against previous end-of-season rates for Week 14, and it is the second highest cumulative in-season hospitalization rate observed in Week 14, following the 2017-2018 season (101.6). Cumulative in-season hospitalization rates observed in Week 14 from 2010-2011 through 2022-2023 ranged from 0.8 to 68.2.

When examining rates by age, the highest cumulative hospitalization rate per 100,000 population was among adults aged 65 years and older (207.5), followed by adults aged 50-64 years (90.2) and children aged 0-4 years (78.0). When examining age-adjusted rates by race and ethnicity, the highest rate of hospitalization per 100,000 population was among non-Hispanic Black persons (139.8), followed by non-Hispanic American Indian or Alaska Native persons (104.8), Hispanic persons (70.8), non-Hispanic White persons (58.5), and non-Hispanic Asian/Pacific Islander persons (39.8).

Among 23,235 hospitalizations, 19,767 (85.1%) were associated with influenza A virus, 3,307 (14.2%) with influenza B virus, 42 (0.2%) with influenza A virus and influenza B virus co-infection, and 118 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,319 (71.0%) were A(H1N1) pdm09 and 1,358 (29.0%) were A(H3N2).

Among 2,879 hospitalized adults with information on underlying medical conditions, 95.4% had at least one reported underlying medical condition, the most commonly reported were hypertension, cardiovascular disease, obesity, and metabolic disease. Among 1,381 hospitalized women of childbearing age (15-49 years) with information on pregnancy status, 22.1% were pregnant. Among 898 hospitalized children with information on underlying medical conditions, 69.5% had at least one reported underlying medical condition; the most commonly reported was asthma, followed by obesity and neurologic disease.



In these figures, cumulative and weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospitals admissions are subject to reporting delays. As hospitalization data are reviewed each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Hospitals report to NHSN the weekly number of patients admitted with laboratory-confirmed influenza. During Week 14, 4,825 patients with laboratory-confirmed influenza were admitted to a hospital. The number of patients admitted to a hospital with laboratory-confirmed influenza for Week 14 decreased (change of >5%) compared to Week 13 nationally and in regions 4, 5, 6, 7, 8, 9, and 10. The number of hospitalizations remained stable in regions 1 and 2 and slightly increased in Region 3.

Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on April 11, 2024, 0.4% of the deaths that occurred during the week ending April 6, 2024 (Week 14), were due to influenza. This percentage remained stable (< 0.1 percentage point change) compared to Week 13. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Five influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 14. The deaths occurred between Week 7 (the week ending February 17, 2024) and Week 13 (the week ending March 30, 2024). Two deaths were associated with influenza A viruses for which no subtyping was performed and three deaths were associated with influenza B viruses with no lineage determined.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated April 19, 2024
fluview-banner2.jpg

Key Updates for Week 15, ending April 13, 2024

Seasonal influenza activity continues to decline in most areas of the country. Viruses


Clinical Lab 5.9%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 2.5%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Activity Map
This week 3 jurisdictions experienced moderate activity and 2 jurisdictions experienced high activity.

FluSurv-NET 77.5 per 100,000


cumulative hospitalization rate.

NHSN Hospitalizations 3,844 (Trend )


patients admitted to hospitals with influenza this week.

NCHS Mortality 0.4%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 4


influenza-associated deaths were reported this week for a total of 142 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity continues to decline nationally and in most areas of the country.
  • Nationally, percent positivity for both influenza A and B decreased compared to last week.
  • Nationally, outpatient respiratory illness declined and is below baseline for the second week in a row.[SUP]1 [/SUP]HHS regions 2, 3, 4, 5, 6, 7, 8, 9, and 10 are below their baselines, while Region 1 remains above its region-specific baselines.
  • Nationally, the number of weekly flu hospital admissions has been decreasing since January.
  • During Week 15, of the 210 viruses reported by public health laboratories, 131 (62.4%) were influenza A and 79 (37.6%) were influenza B. Of the 91 influenza A viruses subtyped during Week 15, 43 (47.3%) were influenza A(H1N1)pdm09 and 48 (52.7%) were A(H3N2).
  • Four influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 15, bringing the season total to 142 pediatric deaths.
  • CDC estimates that there have been at least 33 million illnesses, 370,000 hospitalizations, and 24,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as influenza viruses are spreading.[SUP]2[/SUP] Vaccination can still provide benefit this season.
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories decreased (change of >0.5 percentage points) compared to the previous week. Regions 1, 2, 3, 4, 5, 6, 7, and 10 decreased in percent positivity, while regions 8 and 9 remained stable during Week 15 compared to Week 14. The regions with the highest percent positivity were regions 7 (13.4%), 1 (8.3%), and 5 (8.2%). Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Viruses known to be associated with recent receipt of live attenuated influenza vaccine (LAIV) or found upon further testing to be a vaccine virus are not included, as they are not circulating influenza viruses. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested60,0702,943,347
No. of positive specimens (%)3,569 (5.9%)333,038 (11.3%)
Positive specimens by type
Influenza A1,929 (54.0%)231,132 (69.4%)
Influenza B1,640 (46.0%)101,896 (30.6%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested962100,576
No. of positive specimens21033,071
Positive specimens by type/subtype
Influenza A131 (62.4%)25,433 (76.9%)
Subtyping Performed91 (69.5%)21,112 (83.0%)
(H1N1)pdm0943 (47.3%)14,839 (70.3%)
H3N248 (52.7%)6,273 (29.7%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed40 (30.5%)4,321 (17.0%)
Influenza B79 (37.6%)7,638 (23.1%)
Lineage testing performed58 (73.4%)6,341 (83.0%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage58 (100%)6,341 (100%)
Lineage not performed21 (26.6%)1,297 (17.0%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 3,626 influenza viruses collected since October 1, 2023.
A/H11,457
6B.1A.5a1,457 (100%)2a350 (24.0%)
2a.11,107 (76.0%)
A/H31,173
3C.2a1b.2a1,173 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,170 (99.7%)
2b1 (0.1%)
B/Victoria996
V1A996 (100%)3a.2996 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 244 A(H1N1)pdm09 viruses were antigenically characterized by HI, and 244 (100%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 249 A(H3N2) viruses were antigenically characterized by HI or HINT, and 246 (98.8%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 235 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 01, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested3,6371,4691,178990
Reduced Inhibition1 (0.03%)1 (0.07%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition2 (0.05%)2 (0.1%)0 (0.0%)0 (0.0%)
PeramivirViruses Tested3,6371,4691,178990
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition2 (0.05%)2 (0.1%)0 (0.0%)0 (0.0%)
ZanamivirViruses Tested3,6371,4691,178990
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested3,5191,4121,146961
Decreased Susceptibility1 (0.03%)0 (0.0%)1 (0.09%)0 (0.0%)
Two A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, during Week 15, 2.5% of patient visits reported through ILINet were due to respiratory illness that included fever plus a cough or sore throat, also referred to as ILI. This has decreased (change of > 0.1 percentage points) since Week 14 and is below the national baseline. The percentage of visits for ILI decreased in regions 1, 2, 3, 4, 5, 6, and 7 and remained stable in regions 8, 9, and 10 in Week 15 compared to Week 14. Region 1 is above its region-specific baseline, and all other regions are below their respective baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years, 5-24 years, 25-49 years, and 50-64 years age groups, and remained stable in the 65+ years age groups in Week 15 compared to Week 14.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 15
(Week ending
Apr. 13, 2024)
Week 14
(Week ending
Apr. 6, 2024)
Week 15
(Week ending
Apr. 13, 2024)
Week 14
(Week ending
Apr. 6, 2024)
Very High0000
High22612
Moderate372537
Low111298127
Minimal3834571535
Insufficient Data10229218




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 23,694 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and April 13, 2024. The weekly hospitalization rate observed in Week 15 was 0.9 per 100,000 population. The weekly hospitalization rate peaked this season during Week 52, and is the third highest weekly rate peak observed during all seasons going back to 2010-2011 following the 2014-2015 and 2017-2018 seasons. The overall cumulative hospitalization rate was 77.5 per 100,000 population. This cumulative hospitalization rate is the second highest cumulative hospitalization rate when compared against previous end-of-season rates for Week 15, and it is the second highest cumulative in-season hospitalization rate observed in Week 15, following the 2017-2018 season (103.7). Cumulative in-season hospitalization rates observed in Week 15, from 2010-2011 through 2022-2023 ranged from 0.8 to 68.3.

When examining rates by age, the highest cumulative hospitalization rate per 100,000 population was among adults aged 65 years and older (211.7), followed by adults aged 50-64 years (92.1) and children aged 0-4 years (79.5). When examining age-adjusted rates by race and ethnicity, the highest rate of hospitalization per 100,000 population was among non-Hispanic Black persons (142.4), followed by non-Hispanic American Indian or Alaska Native persons (106.3), Hispanic persons (72.5), non-Hispanic White persons (59.8), and non-Hispanic Asian/Pacific Islander persons (41.3).

Among 23,694 hospitalizations, 20,127 (84.9%) were associated with influenza A virus, 3,403 (14.4%) with influenza B virus, 42 (0.2%) with influenza A virus and influenza B virus co-infection, and 122 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,386 (70.4%) were A(H1N1) pdm09 and 1,421 (29.6%) were A(H3N2).

Among 3,099 hospitalized adults with information on underlying medical conditions, 95.5% had at least one reported underlying medical condition, the most commonly reported were hypertension, cardiovascular disease, obesity, and metabolic disease. Among 1,419 hospitalized women of childbearing age (15-49 years) with information on pregnancy status, 22.1% were pregnant. Among 963 hospitalized children with information on underlying medical conditions, 69.8% had at least one reported underlying medical condition; the most commonly reported was asthma, followed by obesity and neurologic disease.



In these figures, cumulative and weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospitals admissions are subject to reporting delays. As hospitalization data are reviewed each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Hospitals report to NHSN the weekly number of patients admitted with laboratory-confirmed influenza. During Week 15, 3,844 patients with laboratory-confirmed influenza were admitted to a hospital. The number of patients admitted to a hospital with laboratory-confirmed influenza for Week 15 decreased (change of >5%) compared to Week 14 nationally and in regions 1, 2, 3, 4, 5, 6, 7, 8, and 10. The number of hospitalizations remained stable in Region 9.

Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on April 18, 2024, 0.4% of the deaths that occurred during the week ending April 13, 2024 (Week 15), were due to influenza. This percentage increased (≥ 0.1 percentage point change) slightly compared to Week 14. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Four influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 15. The deaths occurred during Week 44 of 2023 (the week ending November 4, 2023) and during weeks 13 and 14 of 2024 (the weeks ending March 30, 2024, and April 6, 2024). Two deaths were associated with influenza A viruses and two deaths were associated with influenza B viruses with no lineage determined. Both influenza A viruses had subtyping performed; one was an A(H1N1) virus and one was an A(H3) virus.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated April 26, 2024
fluview-banner2.jpg

Key Updates for Week 16, ending April 20, 2024

Seasonal influenza activity continues to decline in most areas of the country. Viruses


Clinical Lab 4.8%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 2.3%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Activity Map
1 moderate jurisdiction

FluSurv-NET 79.0 per 100,000


cumulative hospitalization rate.

NHSN Hospitalizations 2,762 (Trend )


patients admitted to hospitals with influenza this week.

NCHS Mortality 0.3%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 6


influenza-associated deaths were reported this week for a total of 148 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity continues to decline nationally and in most areas of the country.
  • Nationally, percent positivity for both influenza A and B decreased compared to last week.
  • Nationally, outpatient respiratory illness declined and is below baseline for the third week in a row.[SUP]1 [/SUP]HHS regions 2, 3, 4, 5, 6, 7, 8, 9, and 10 are below their baselines, while Region 1 is at its region-specific baseline.
  • Nationally, the number of weekly flu hospital admissions has been decreasing since January.
  • During Week 16, of the 185 viruses reported by public health laboratories, 116 (62.7%) were influenza A and 69 (37.3%) were influenza B. Of the 63 influenza A viruses subtyped during Week 16, 21 (33.3%) were influenza A(H1N1)pdm09 and 42 (66.7%) were A(H3N2).
  • Six influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 16, bringing the season total to 148 pediatric deaths.
  • CDC estimates that there have been at least 34 million illnesses, 380,000 hospitalizations, and 24,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as flu activity continues.[SUP]2[/SUP]
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories decreased (change of >0.5 percentage points) compared to the previous week. Regions 1, 2, 3, 5, 6, 7, and 8 decreased in percent positivity, Region 9 slightly increased in percent positivity while regions 4 and 10 remained stable during Week 16 compared to Week 15. The regions with the highest percent positivity were regions 7 (9.7%), 1 (6.5%), and 5 (5.9%). Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Viruses known to be associated with recent receipt of live attenuated influenza vaccine (LAIV) or found upon further testing to be a vaccine virus are not included, as they are not circulating influenza viruses. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested56,2062,989,749
No. of positive specimens (%)2,720 (4.8%)336,223 (11.2%)
Positive specimens by type
Influenza A1,532 (56.3%)232,930 (69.3%)
Influenza B1,188 (43.7%)103,282 (30.7%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested900102,610
No. of positive specimens18533,910
Positive specimens by type/subtype
Influenza A116 (62.7%)25,982 (76.6%)
Subtyping Performed63 (54.3%)21,493 (82.7%)
(H1N1)pdm0921 (33.3%)14,982 (69.7%)
H3N242 (66.7%)6,511 (30.3%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed53 (45.7%)4,489 (17.3%)
Influenza B69 (37.3%)7,928 (23.4%)
Lineage testing performed39 (56.5%)6,561 (82.8%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage39 (100.0%)6,561 (100.0%)
Lineage not performed30 (43.5%)1,367 (17.2%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 3,842 influenza viruses collected since October 1, 2023.
A/H11,457
6B.1A.5a1,457 (100%)2a350 (24.0%)
2a.11,107 (76.0%)
A/H31,173
3C.2a1b.2a1,173 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,170 (99.7%)
2b1 (0.1%)
B/Victoria996
V1A996 (100%)3a.2996 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 244 A(H1N1)pdm09 viruses were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 265 A(H3N2) viruses were antigenically characterized by HI or HINT, and 262 (98.7%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 235 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested3,9111,5521,2761,083
Reduced Inhibition1 (0.03%)1 (0.06%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition2 (0.05%)2 (0.1%)0 (0.0%)0 (0.0%)
PeramivirViruses Tested3,9111,5521,2761,083
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition2 (0.05%)2 (0.1%)0 (0.0%)0 (0.0%)
ZanamivirViruses Tested3,9111,5521,2761,083
Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
Highly Reduced Inhibition0 (0.0%)0 (0.0%)0 (0.0%)0 (0.0%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested3,7921,5031,2371,052
Decreased Susceptibility1 (0.03%)0 (0.0%)1 (0.08%)0 (0.0%)
Two A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, during Week 16, 2.3% of patient visits reported through ILINet were due to respiratory illness that included fever plus a cough or sore throat, also referred to as ILI. This has decreased (change of > 0.1 percentage points) since Week 15 and is below the national baseline. The percentage of visits for ILI decreased in regions 1, 2, 3, 4, 5, 6, 8, 9, and 10 and remained stable in Region 7 in Week 16 compared to Week 15. Region 1 is at its region-specific baseline, and all other regions are below their respective baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years, 5-24 years, 25-49 years, and 50-64 years age groups, and remained stable in the 65+ years age groups in Week 16 compared to Week 15.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 16
(Week ending
Apr. 20, 2024)
Week 15
(Week ending
Apr. 13, 2024)
Week 16
(Week ending
Apr. 20, 2024)
Week 15
(Week ending
Apr. 13, 2024)
Very High0000
High0115
Moderate14824
Low7115999
Minimal4639626577
Insufficient Data10235224




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 24,140 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and April 20, 2024. The weekly hospitalization rate observed in Week 16 was 0.7 per 100,000 population. The weekly hospitalization rate observed during Week 52 is tied with the 2014-2015 season for the second highest peak weekly rate observed during all seasons going back to 2010-2011 and only lower than the 2017-2018 season. The overall cumulative hospitalization rate was 79.0 per 100,000 population. This cumulative hospitalization rate is the second highest cumulative hospitalization rate when compared against previous end-of-season rates for Week 16, and it is the second highest cumulative in-season hospitalization rate observed in Week 16, following the 2017-2018 season (105.3). Cumulative in-season hospitalization rates observed in Week 16, from 2010-2011 through 2022-2023 (excluding the 2017-2018 season) ranged from 0.8 to 68.6.

When examining rates by age, the highest cumulative hospitalization rate per 100,000 population was among adults aged 65 years and older (215.8) followed by adults aged 50-64 years (93.8) and children aged 0-4 years (80.9). When examining age-adjusted rates by race and ethnicity, the highest rate of hospitalization per 100,000 population was among non-Hispanic Black persons (144.3), followed by non-Hispanic American Indian or Alaska Native persons (108.2), Hispanic persons (73.7), non-Hispanic White persons (60.9), and non-Hispanic Asian/Pacific Islander persons (41.8).

Among 24,140 hospitalizations, 20,474 (84.8%) were associated with influenza A virus, 3,495 (14.5%) with influenza B virus, 45 (0.2%) with influenza A virus and influenza B virus co-infection, and 126 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,426 (70.2%) were A(H1N1) pdm09 and 1,453 (29.8%) were A(H3N2).

Among 3,259 hospitalized adults with information on underlying medical conditions, 95.6% had at least one reported underlying medical condition; the most commonly reported were hypertension, cardiovascular disease, obesity, and metabolic disease. Among 1,449 hospitalized women of childbearing age (15-49 years) with information on pregnancy status, 22.2% were pregnant. Among 991 hospitalized children with information on underlying medical conditions, 68.8% had at least one reported underlying medical condition; the most commonly reported was asthma, followed by obesity and neurologic disease.



In these figures, cumulative and weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospitals admissions are subject to reporting delays. As hospitalization data are reviewed each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Hospitals report to NHSN the weekly number of patients admitted with laboratory-confirmed influenza. During Week 16, 2,762 patients with laboratory-confirmed influenza were admitted to a hospital. The number of patients admitted to a hospital with laboratory-confirmed influenza for Week 16 decreased (change of >5%) compared to Week 15 nationally and in all 10 regions.

Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. After May 3, 2024, the NHSN flu hospitalization data will not be included in FluView/FluView Interactive for the remainder of the 2023-2024 season.

Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on April 25, 2024, 0.3% of the deaths that occurred during the week ending April 20, 2024 (Week 16), were due to influenza. This percentage remained stable (< 0.1 percentage point change) compared to Week 15. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Six influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 16. The deaths occurred during weeks 46 and 50 of 2023 (the weeks ending November 18 and December 16 of 2023) and during weeks 3, 7, 8, and 14 of 2024 (the weeks ending January 20, February 17, February 24, and April 6 of 2024, respectively). Three deaths were associated with influenza A viruses for which subtyping was not performed, and three deaths were associated with influenza B viruses. Two of the influenza B viruses had lineage determined, and both were B/Victoria viruses.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated May 3, 2024
fluview-banner2.jpg

Key Updates for Week 17, ending April 27, 2024

Seasonal influenza activity continues to decline in most areas of the country. Viruses


Clinical Lab 3.9%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 2.2%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Activity Map
0 moderate jurisdictions and 0 high or very high jurisdictions

FluSurv-NET 79.8 per 100,000


cumulative hospitalization rate.

NHSN Hospitalizations 2,302 (Trend )


patients admitted to hospitals with influenza this week.

NCHS Mortality 0.2%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 10


influenza-associated deaths were reported this week for a total of 158 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity continues to decline nationally and in most areas of the country.
  • Nationally, percent positivity for both influenza A and B decreased compared to last week.
  • Nationally, outpatient respiratory illness remained stable and is below baseline for the fourth week in a row.[SUP]1 [/SUP]All 10 HHS regions are below their region-specific baselines.
  • Nationally, the number of weekly flu hospital admissions has been decreasing since January.
  • During Week 17, of the 157 viruses reported by public health laboratories, 101 (64.3%) were influenza A and 56 (35.7%) were influenza B. Of the 69 influenza A viruses subtyped during Week 17, 23 (33.3%) were influenza A(H1N1)pdm09 and 46 (66.7%) were A(H3N2).
  • Ten influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 17, bringing the season total to 158 pediatric deaths.
  • CDC estimates that there have been at least 34 million illnesses, 380,000 hospitalizations, and 24,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as flu activity continues.[SUP]2[/SUP]
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories decreased (change of >0.5 percentage points) compared to the previous week. Regions 1, 2, 3, 5, 6, 7, and 8 decreased in percent positivity while regions 4, 9, and 10 remained stable during Week 17 compared to Week 16. The regions with the highest percent positivity were regions 7 (5.9%), 1 (5.0%), and 5 (4.4%). Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Viruses known to be associated with recent receipt of live attenuated influenza vaccine (LAIV) or found upon further testing to be a vaccine virus are not included, as they are not circulating influenza viruses. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested58,8443,084,016
No. of positive specimens (%)2,263 (3.8%)339,304 (11.0%)
Positive specimens by type
Influenza A1,323 (58.5%)234,716 (69.2%)
Influenza B940 (41.5%)104,577 (30.8%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested915104,214
No. of positive specimens15734,456
Positive specimens by type/subtype
Influenza A101 (64.3%)26,333 (76.4%)
Subtyping Performed69 (68.3%)21,818 (82.9%)
(H1N1)pdm0923 (33.3%)15,115 (69.3%)
H3N246 (66.7%)6,703 (30.7%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed32 (31.7%)4,515 (17.1%)
Influenza B56 (35.7%)8,123 (23.6%)
Lineage testing performed29 (51.8%)6,716 (82.7%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage29 (100.0%)6,716 (100.0%)
Lineage not performed27 (48.2%)1,407 (17.3%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 4,012 influenza viruses collected since October 1, 2023.
A/H11,582
6B.1A.5a1,582 (100%)2a366 (23.1%)
2a.11,216 (76.9%)
A/H31,293
3C.2a1b.2a1,293 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,290 (99.7%)
2b1 (0.1%)
B/Victoria1,137
V1A1,137 (100%)3a.21,137 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 325 A(H1N1)pdm09 viruses were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 306 A(H3N2) viruses were antigenically characterized by HI or HINT, and 302 (98.7%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 235 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested4,0111,5851,2931,133
Reduced Inhibition1 (0.02%)1 (0.06%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition2 (0.05%)2 (0.1%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested4,0111,5851,2931,133
Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition2 (0.05%)2 (0.1%)0 (0.00%)0 (0.00%)
ZanamivirViruses Tested4,0111,5851,2931,133
Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested3,8871,5341,2541,099
Decreased Susceptibility1 (0.03%)0 (0.0%)1 (0.1%)0 (0.0%)
Two A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, during Week 17, 2.2% of patient visits reported through ILINet were due to respiratory illness that included fever plus a cough or sore throat, also referred to as ILI. This has remained stable (change of ≤ 0.1 percentage points) since Week 16 and is below the national baseline. The percentage of visits for ILI decreased in regions 1, 2, 7, and 8 and remained stable in regions 3, 4, 6, 9, and 10 in Week 17 compared to Week 16. All 10 regions are below their respective baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet remained stable in all age groups in Week 17 compared to Week 16.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 17
(Week ending
Apr. 27, 2024)
Week 16
(Week ending
Apr. 20, 2024)
Week 17
(Week ending
Apr. 27, 2024)
Week 16
(Week ending
Apr. 20, 2024)
Very High0000
High0031
Moderate01411
Low584957
Minimal4945645639
Insufficient Data11228221




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 24,385 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and April 27, 2024. The weekly hospitalization rate observed in Week 17 was 0.5 per 100,000 population. The weekly hospitalization rate observed during Week 52 is tied with the 2014-2015 season for the second highest peak weekly rate observed during all seasons going back to 2010-2011, and only lower than the 2017-2018 season. The overall cumulative hospitalization rate was 79.8 per 100,000 population. This cumulative hospitalization rate is the second highest cumulative hospitalization rate when compared against previous end-of-season rates for Week 17, and it is the second highest cumulative in-season hospitalization rate observed in Week 17, following the 2017-2018 season (106.0). Cumulative in-season hospitalization rates observed in Week 17, from 2010-2011 through 2022-2023 (excluding 2017-2018) ranged from 0.8 to 69.0.

When examining rates by age, the highest cumulative hospitalization rate per 100,000 population was among adults aged 65 years and older (218.2), followed by adults aged 50-64 years (94.7) and children aged 0-4 years (82.0). When examining age-adjusted rates by race and ethnicity, the highest rate of hospitalization per 100,000 population was among non-Hispanic Black persons (145.5), followed by non-Hispanic American Indian or Alaska Native persons (109.7), Hispanic persons (75.4), non-Hispanic White persons (61.6), and non-Hispanic Asian/Pacific Islander persons (42.9).

Among 24,385 hospitalizations, 20,666 (84.7%) were associated with influenza A virus, 3,546 (14.5%) with influenza B virus, 46 (0.2%) with influenza A virus and influenza B virus co-infection, and 127 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,487 (69.9%) were A(H1N1) pdm09 and 1,501 (30.1%) were A(H3N2).

Among 3,450 hospitalized adults with information on underlying medical conditions, 95.6% had at least one reported underlying medical condition, the most commonly reported were hypertension, cardiovascular disease, obesity, and metabolic disease. Among 1,509 hospitalized women of childbearing age (15-49 years) with information on pregnancy status, 22.7% were pregnant. Among 1,015 hospitalized children with information on underlying medical conditions, 68.6% had at least one reported underlying medical condition; the most commonly reported was asthma, followed by obesity and neurologic disease.



In these figures, cumulative and weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospitals admissions are subject to reporting delays. As hospitalization data are reviewed each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Hospitals report to NHSN the weekly number of patients admitted with laboratory-confirmed influenza. During Week 17, 2,302 patients with laboratory-confirmed influenza were admitted to a hospital. The number of patients admitted to a hospital with laboratory-confirmed influenza for Week 17 decreased (change of >5%) compared to Week 16 nationally and in regions 1, 2, 3, 4, 5, 6, 7, and 8. The number of hospitalizations reported in regions 9 and 10 increased slightly compared to last week.

Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. After May 3, 2024, the NHSN flu hospitalization data will not be included in FluView/FluView Interactive for the remainder of the 2023-2024 season.

Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on May 2, 2024, 0.2% of the deaths that occurred during the week ending April 27, 2024 (Week 17), were due to influenza. This percentage decreased (≥ 0.1 percentage point change) compared to Week 16. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Ten influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 17. The deaths occurred between weeks 1 and 10 (the weeks ending January 6, 2024, and March 9, 2024) and during Week 16 (the week ending April 20, 2024). Six deaths were associated with influenza A viruses. Four of the influenza A viruses had subtyping performed; three were A(pdm09H1N1) viruses and one was an A(H3N2) virus. Three deaths were associated with influenza B viruses with no lineage determined. Lastly, one death was associated with a co-infection of influenza A and B viruses.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated May 10, 2024
fluview-banner2.jpg

Key Updates for Week 18, ending May 4, 2024

Seasonal influenza activity continues to decline in most areas of the country. Viruses


Clinical Lab 3.1%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 2.1%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Activity Map
This week no jurisdictions experienced moderate, high, or very high activity.

FluSurv-NET 80.3 per 100,000


cumulative hospitalization rate.

NHSN Hospitalizations
Mandatory reporting is no longer required.

NCHS Mortality 0.2%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 7


influenza-associated deaths were reported (1 occurred during 2022-2023 season and 6 occurred during 2023-2024 season)

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity continues to decline nationally and in most areas of the country.
  • Nationally, outpatient respiratory illness remained stable and is below baseline for the fifth week in a row.[SUP]1 [/SUP]All 10 HHS regions are below their region-specific baselines.
  • During Week 18, of the 109 viruses reported by public health laboratories, 77 (70.6%) were influenza A and 32 (29.4%) were influenza B. Of the 54 influenza A viruses subtyped during Week 18, 25 (46.3%) were influenza A(H1N1)pdm09 and 29 (53.7%) were A(H3N2).
  • Six influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 18, bringing the season total to 164 pediatric deaths.
  • CDC estimates that there have been at least 34 million illnesses, 380,000 hospitalizations, and 24,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as flu activity continues.[SUP]2[/SUP]
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories decreased (change of >0.5 percentage points) compared to the previous week. Regions 3, 5, 7, and 10 decreased in percent positivity while regions 1, 2, 4, 6, 8, and 9 remained stable during Week 18 compared to Week 17. The regions with the highest percent positivity were regions 1 (4.9%), 7 (4.4%), and 9 (3.9%). Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Viruses known to be associated with recent receipt of live attenuated influenza vaccine (LAIV) or found upon further testing to be a vaccine virus are not included, as they are not circulating influenza viruses. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested46,2453,117,205
No. of positive specimens (%)1,426 (3.1%)340,899 (10.9%)
Positive specimens by type
Influenza A839 (58.8%)235,659 (69.1%)
Influenza B587 (41.2%)105,229 (30.9%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested787105,685
No. of positive specimens10934,984
Positive specimens by type/subtype
Influenza A77 (70.6%)26,681 (76.3%)
Subtyping Performed54 (70.1%)22,074 (82.7%)
(H1N1)pdm0925 (46.3%)15,231 (69.0%)
H3N229 (53.7%)6,843 (31.0%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed23 (29.9%)4,607 (17.3%)
Influenza B32 (29.4%)8,303 (23.7%)
Lineage testing performed18 (56.3%)6,884 (82.9%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage18 (100.0%)6,884 (100.0%)
Lineage not performed14 (43.8%)1,419 (17.1%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 4,257 influenza viruses collected since October 1, 2023.
A/H11,638
6B.1A.5a1,638 (100%)2a375 (22.9%)
2a.11,263 (77.1%)
A/H31,429
3C.2a1b.2a1,429 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,426 (99.8%)
2b1 (0.1%)
B/Victoria1,190
V1A1,190 (100%)3a.21,190 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 364 A(H1N1)pdm09 viruses were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 349 A(H3N2) viruses were antigenically characterized by HI or HINT, and 342 (98.0%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 264 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested4,2611,6421,4321,187
Reduced Inhibition1 (0.02%)1 (0.1%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition2 (0.05%)2 (0.1%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested4,2611,6421,4321,187
Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition2 (0.05%)2 (0.1%)0 (0.00%)0 (0.00%)
ZanamivirViruses Tested4,2611,6421,4321,187
Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested4,1391,5891,3941,156
Decreased Susceptibility1 (0.02%)0 (0.0%)1 (0.1%)0 (0.0%)
Two A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, during Week 18, 2.1% of patient visits reported through ILINet were due to respiratory illness that included fever plus a cough or sore throat, also referred to as ILI. This has remained stable (change of ≤ 0.1 percentage points) since Week 17 and is below the national baseline. The percentage of visits for ILI decreased in regions 5 and 7 and remained stable in all other regions in Week 18 compared to Week 17. All 10 regions are below their respective baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet remained stable in all age groups in Week 18 compared to Week 17.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 18
(Week ending
May 4, 2024)
Week 17
(Week ending
Apr. 27, 2024)
Week 18
(Week ending
May 4, 2024)
Week 17
(Week ending
Apr. 27, 2024)
Very High0000
High0014
Moderate0063
Low363249
Minimal5249654649
Insufficient Data00236224




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 24,547 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and May 4, 2024. The weekly hospitalization rate observed in Week 18 was 0.3 per 100,000 population The weekly hospitalization rate observed during Week 52 is tied with the 2014-2015 season for the second highest peak weekly rate observed during all seasons going back to 2010-2011, and only lower than the 2017-2018 season. The overall cumulative hospitalization rate was 80.3 per 100,000 population. This cumulative hospitalization rate is the second highest cumulative hospitalization rate when compared against previous end-of-season rates for Week 18, and it is the second highest cumulative in-season hospitalization rate observed in Week 18, following the 2017-2018 season (106.7). Cumulative in-season hospitalization rates observed in Week 18, from 2010-2011 through 2022-2023 (excluding the 2017-2018 season) ranged from 0.8 to 69.4.

When examining rates by age, the highest cumulative hospitalization rate per 100,000 population was among adults aged 65 years and older (219.8) followed by adults aged 50-64 years (95.2) and children aged 0-4 years (82.6). When examining age-adjusted rates by race and ethnicity, the highest rate of hospitalization per 100,000 population was among non-Hispanic Black persons (146.1), followed by non-Hispanic American Indian or Alaska Native persons (110.9), Hispanic persons (76.0), non-Hispanic White persons (62.1), and non-Hispanic Asian/Pacific Islander persons (43.3).

Among 24,547 hospitalizations, 20,782 (84.7%) were associated with influenza A virus, 3,588 (14.6%) with influenza B virus, 48 (0.2%) with influenza A virus and influenza B virus co-infection, and 125 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,551 (69.4%) were A(H1N1) pdm09 and 1,566 (30.6%) were A(H3N2).

Among 3,689 hospitalized adults with information on underlying medical conditions, 95.4% had at least one reported underlying medical condition, the most commonly reported were hypertension, cardiovascular disease, obesity, and metabolic disease. Among 1,553 hospitalized women of childbearing age (15-49 years) with information on pregnancy status, 22.7% were pregnant. Among 1,049 hospitalized children with information on underlying medical conditions, 67.9% had at least one reported underlying medical condition; the most commonly reported was asthma, followed by obesity and neurologic disease.



In these figures, cumulative and weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospitals admissions are subject to reporting delays. As hospitalization data are reviewed each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. After May 3, 2024, NHSN flu hospitalization data will not be included in FluView/FluView Interactive for the remainder of the 2023-2024 season.
Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on May 9, 2024, 0.2% of the deaths that occurred during the week ending May 4, 2024 (Week 18), were due to influenza. This percentage remained stable (< 0.1 percentage point change) compared to Week 17. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Seven influenza-associated pediatric deaths were reported to CDC during Week 18.

Six deaths occurred during the 2023-2024 season, bringing the total pediatric deaths for this season to 164. The deaths occurred during Week 49 of 2023 (the week ending December 9, 2023) and between weeks 7 and 14 of 2024 (the weeks ending February 17, 2024, and April 6, 2024). Two deaths were associated with influenza A viruses and four deaths were associated with influenza B viruses with no lineage determined. One of the influenza A viruses had subtyping performed and it was an A(H3N2) virus.

One death occurring during the 2022-2023 season was also reported, which brings the total number of pediatric deaths for last season to 185. The death was associated with an influenza A(H3N2) virus and occurred during Week 45 of 2022 (the week ending November 12, 2022).

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated May 17, 2024
fluview-banner2.jpg

Key Updates for Week 19, ending May 11, 2024

Seasonal influenza activity is low nationally. Viruses


Clinical Lab 2.4%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 2.0%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Map
This week no jurisdictions experienced moderate, high, or very high activity.

FluSurv-NET 80.6 per 100,000


cumulative hospitalization rate.

NCHS Mortality 0.1%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 3


influenza-associated deaths were reported this week for a total of 167 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity is low nationally.
  • Nationally, outpatient respiratory illness remained stable and is below baseline for the sixth week in a row.[SUP]1 [/SUP]All 10 HHS regions are below their region-specific baselines.
  • During Week 19, of the 94 viruses reported by public health laboratories, 57 (60.6%) were influenza A and 37 (39.4%) were influenza B. Of the 43 influenza A viruses subtyped during Week 19, 17 (39.5%) were influenza A(H1N1)pdm09 and 26 (60.5%) were A(H3N2).
  • Three influenza-associated pediatric deaths were reported to CDC during Week 19, bringing the season total to 167 pediatric deaths.
  • CDC estimates that there have been at least 35 million illnesses, 390,000 hospitalizations, and 24,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as flu activity continues.[SUP]2[/SUP]
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Seasonal flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories decreased (change of >0.5 percentage points) compared to the previous week. Regions 1, 2, 3, 5, 6, 7, and 8 decreased in percent positivity while regions 4 and 9 remained stable and Region 10 increased slightly during Week 19 compared to Week 18. The regions with the highest percent positivity were regions 10 (4.4%), 9 (4.0%), and 7 (3.1%). Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Viruses known to be associated with recent receipt of live attenuated influenza vaccine (LAIV) or found upon further testing to be a vaccine virus are not included, as they are not circulating influenza viruses. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested44,0713,208,299
No. of positive specimens (%)1,048 (2.4%)343,365 (10.7%)
Positive specimens by type
Influenza A676 (64.5%)236,845 (69.0%)
Influenza B372 (35.5%)106,509 (31.0%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested796107,016
No. of positive specimens9435,385
Positive specimens by type/subtype
Influenza A57 (60.6%)26,958 (76.2%)
Subtyping Performed43 (75.4%)22,327 (82.8%)
(H1N1)pdm0917 (39.5%)15,333 (68.7%)
H3N226 (60.5%)6,994 (31.3%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed14 (24.6%)4,631 (17.2%)
Influenza B37 (39.4%)8,427 (23.8%)
Lineage testing performed13 (35.1%)6,994 (83.0%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage13 (100.0%)6,994 (100.0%)
Lineage not performed24 (64.9%)1,433 (17.0%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 4,374 influenza viruses collected since October 1, 2023.
A/H11,673
6B.1A.5a1,673 (100%)2a387 (23.1%)
2a.11,286 (76.9%)
A/H31,466
3C.2a1b.2a1,466 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,463 (99.8%)
2b1 (0.1%)
B/Victoria1,235
V1A1,235 (100%)3a.21,235 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 387 A(H1N1)pdm09 viruses were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 371 A(H3N2) viruses were antigenically characterized by HI or HINT, and 364 (98.1%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 264 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested4,2791,6481,4381,193
Reduced Inhibition1 (0.02%)1 (0.06%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition2 (0.05%)2 (0.1%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested4,2791,6481,4381,193
Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition2 (0.05%)2 (0.1%)0 (0.00%)0 (0.00%)
ZanamivirViruses Tested4,2791,6481,4381,193
Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested4,1551,5941,3991,162
Decreased Susceptibility1 (0.02%)0 (0.0%)1 (0.1%)0 (0.0%)
Two A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, during Week 19, 2.0% of patient visits reported through ILINet were due to respiratory illness that included fever plus a cough or sore throat, also referred to as ILI. This has remained stable (change of ≤ 0.1 percentage points) since Week 18 and is below the national baseline. The percentage of visits for ILI decreased in regions 1 and 5 and remained stable in all other regions in Week 19 compared to Week 18. All 10 regions are below their respective baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years and 5-24 years age groups and remained stable in all other age groups in Week 19 compared to Week 18.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 19
(Week ending
May 11, 2024)
Week 18
(Week ending
May 4, 2024)
Week 19
(Week ending
May 11, 2024)
Week 18
(Week ending
May 4, 2024)
Very High0000
High0011
Moderate0016
Low443633
Minimal5151655657
Insufficient Data00236232




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 24,643 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and May 11, 2024. The weekly hospitalization rate observed in Week 19 was 0.2 per 100,000 population. The weekly hospitalization rate observed during Week 52 is tied with the 2014-2015 season for the second highest peak weekly rate observed during all seasons going back to 2010-2011 and only lower than the 2017-2018 season. The overall cumulative hospitalization rate was 80.6 per 100,000 population.

When examining rates by age, the highest cumulative hospitalization rate per 100,000 population was among adults aged 65 years and older (220.7) followed by adults aged 50-64 years (95.6) and children aged 0-4 years (82.9). When examining age-adjusted rates by race and ethnicity, the highest rate of hospitalization per 100,000 population was among non-Hispanic Black persons (146.7), followed by non-Hispanic American Indian or Alaska Native persons (111.9), Hispanic persons (76.6), non-Hispanic White persons (62.3), and non-Hispanic Asian/Pacific Islander persons (43.6).

Among 24,643 hospitalizations, 20,857 (84.6%) were associated with influenza A virus, 3,609 (14.7%) with influenza B virus, 48 (0.2%) with influenza A virus and influenza B virus co-infection, and 128 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,563 (69.3%) were A(H1N1) pdm09 and 1,578 (30.7%) were A(H3N2).

Among 3,845 hospitalized adults with information on underlying medical conditions, 95.4% had at least one reported underlying medical condition, the most commonly reported were hypertension, cardiovascular disease, obesity, and metabolic disease. Among 1,582 hospitalized women of childbearing age (15-49 years) with information on pregnancy status, 22.9% were pregnant. Among 1,085 hospitalized children with information on underlying medical conditions, 67.7% had at least one reported underlying medical condition; the most commonly reported was asthma, followed by obesity and neurologic disease.



In these figures, cumulative and weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospitals admissions are subject to reporting delays. As hospitalization data are reviewed each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. Voluntarily reported NHSN hospital data can found at Weekly United States Hospitalization Metrics by Jurisdiction.
Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on May 16, 2024, 0.1% of the deaths that occurred during the week ending May 11, 2024 (Week 19), were due to influenza. This percentage remained stable (< 0.1 percentage point change) compared to Week 18. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Three influenza-associated pediatric deaths were reported to CDC during Week 19, bringing the total pediatric deaths for this season to 167. The deaths occurred during weeks 1, 9, and 12 of 2024 (the weeks ending January 6, March 2, and March 23, 2024). Two deaths were associated with influenza A viruses and one death was associated with an influenza B/Victoria virus. One of the influenza A viruses had subtyping performed and was an A(H3N2) virus.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated May 24, 2024
fluview-banner2.jpg

Key Updates for Week 20, ending May 18, 2024

Seasonal influenza activity is low nationally. Viruses


Clinical Lab 2.0%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 2.0%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Map
2 Moderate

0 High or Very High

FluSurv-NET 0.2 per 100,000


weekly hospitalization rate.

NCHS Mortality 0.1%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 2


influenza-associated deaths were reported this week for a total of 169 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains low nationally.
  • Nationally, outpatient respiratory illness remained stable and is below baseline for the seventh week in a row.[SUP]1 [/SUP]All 10 HHS regions are below their region-specific baselines.
  • One human infection with an influenza A(H5N1) virus was reported by the Michigan Department of Health.
  • During Week 20, of the 64 viruses reported by public health laboratories, 49 (76.6%) were influenza A and 15 (23.4%) were influenza B. Of the 38 influenza A viruses subtyped during Week 20, 15 (39.5%) were influenza A(H1N1)pdm09 and 23 (60.5%) were A(H3N2).
  • Two influenza-associated pediatric deaths were reported to CDC during Week 20, bringing the season total to 169 pediatric deaths.
  • CDC estimates that there have been at least 35 million illnesses, 390,000 hospitalizations, and 25,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as flu activity continues.[SUP]2[/SUP]
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Seasonal flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories remained stable (change of ≤0.5 percentage points) compared to the previous week. Regions 1, 2, 7, and 9 decreased in percent positivity while regions 3, 4, 5, 6, 8, and 10 remained stable during Week 20 compared to Week 19. The regions with the highest percent positivity were regions 10 (4.8%), 9 (2.9%), and 8 (2.0%). Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Viruses known to be associated with recent receipt of live attenuated influenza vaccine (LAIV) or found upon further testing to be a vaccine virus are not included, as they are not circulating influenza viruses. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested35,9463,234,435
No. of positive specimens (%)731 (2.0%)344,458 (10.6%)
Positive specimens by type
Influenza A462 (63.2%)237,465 (68.9%)
Influenza B269 (36.8%)106,982 (31.1%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested594108,684
No. of positive specimens6436,220
Positive specimens by type/subtype
Influenza A49 (76.6%)27,548 (76.1%)
Subtyping Performed38 (77.6%)23,228 (84.3%)
(H1N1)pdm0915 (39.5%)15,763 (67.9%)
H3N223 (60.5%)7,465 (32.1%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed11 (22.4%)4,320 (15.7%)
Influenza B15 (23.4%)8,672 (23.9%)
Lineage testing performed5 (33.3%)7,553 (87.1%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage5 (100.0%)7,553 (100.0%)
Lineage not performed10 (66.7%)1,119 (12.9%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Novel Influenza A Virus


A human infection with highly pathogenic avian influenza (HPAI) A(H5N1) virus was reported by the Michigan Department of Health and Human Services.

A patient aged >18 years in Michigan developed conjunctivitis while working at a commercial dairy farm where HPAI A(H5N1) virus had been detected in cows. The patient reported their symptom onset to the Michigan Department of Health and Human Services via a text-based symptom monitoring system. Respiratory and conjunctival swab specimens were collected from the patient. The respiratory specimen (a nasopharyngeal swab) tested negative for influenza A virus at the Michigan Public Health Laboratory using a Centers for Disease Control and Prevention (CDC) assay. Both specimens were sent to CDC for further testing, where they were received and tested on May 21, 2024. The conjunctival specimen was positive for A(H5N1) virus using diagnostic RT-PCR and sequencing, and the respiratory specimen tested negative for influenza A and A(H5) virus. The patient did not report symptoms other than eye redness, discharge, and discomfort consistent with conjunctivitis, was not hospitalized, and has fully recovered. (https://www.cdc.gov/flu/avianflu/clinicians-evaluating-patients.htm).

In response to this detection, public health officials are conducting surveillance in the area and additional case investigation activities, including contact tracing. Additional symptomatic persons among workers exposed to infected cattle at the same farm have not been identified through monitoring of workers. Additional cases of human infection with A(H5) virus associated with this case and human-to-human transmission of A(H5) virus have not been identified to date.

This is the third person to test positive for A(H5) virus in the United States. The first was reported in April 2022 in Colorado in a person who reported fatigue during culling of poultry infected with HPAI A(H5N1) virus, and the second was reported in April 2024 in a dairy farm worker with conjunctivitis in Texas. This is the second case associated with an ongoing multistate outbreak of HPAI A(H5N1) in dairy cows.

Currently in the United States, HPAI A(H5N1) virus detections among wild birds are widespread. There are outbreaks among animals including poultry, backyard flocks, and dairy cows. Sporadic infections in wild mammals also have been reported by United States Department of Agriculture (USDA) Animal Plant Health Inspection Service (APHIS).

CDC recommends that state and local public health departments monitor people who are exposed to birds or other animals (including livestock) infected or suspected to be infected with avian influenza A viruses for onset of signs and symptoms for 10 days after their last exposure and that people who develop signs or symptoms of respiratory illness and/or conjunctivitis be tested for influenza. Between February 9, 2022 and May 21, 2024, more than 9,000 people were actively monitored following HPAI exposure.

Information about avian influenza is available at https://www.cdc.gov/flu/avianflu/index.htm.

Interim recommendations for Prevention, Monitoring, and Public Health Investigations are available at https://www.cdc.gov/flu/avianflu/hpai/hpai-interim-recommendations.html.

The latest case reports on avian influenza outbreaks in wild birds, commercial poultry, backyard or hobbyist flocks, and mammals in the U.S. are available from the USDA at https://www.aphis.usda.gov/aphis/ou...e-information/avian/avian-influenza/2022-hpai.

Additional information regarding human infections with novel influenza A viruses:

Surveillance Methods | FluView Interactive Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 4,540 influenza viruses collected since October 1, 2023.
A/H11,725
6B.1A.5a1,725 (100%)2a398 (23.1%)
2a.11,327 (76.9%)
A/H31,529
3C.2a1b.2a1,529 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,526 (99.8%)
2b1 (0.1%)
B/Victoria1,286
V1A1,286 (100%)3a.21,286 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 398 A(H1N1)pdm09 viruses were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 405 A(H3N2) viruses were antigenically characterized by HI or HINT, and 394 (97.3%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 281 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested4,5301,7261,5271,277
Reduced Inhibition1 (0.02%)1 (0.1%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition2 (0.04%)2 (0.1%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested4,5301,7261,5271,277
Reduced Inhibition1 (0.02%)0 (0.00%)0 (0.00%)1 (0.1%)
Highly Reduced Inhibition2 (0.04%)2 (0.1%)0 (0.00%)0 (0.00%)
ZanamivirViruses Tested4,5301,7261,5271,277
Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested4,3971,6701,4861,241
Decreased Susceptibility1 (0.02%)0 (0.0%)1 (0.1%)0 (0.0%)
Two A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. One B virus had NA-A245G amino acid substitution and showed reduced inhibition by peramivir.

One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, during Week 20, 2.0% of patient visits reported through ILINet were due to respiratory illness that included fever plus a cough or sore throat, also referred to as ILI. This has remained stable (change of ≤ 0.1 percentage points) since Week 19 and is below the national baseline. The percentage of visits for ILI decreased in regions 8 and 10, increased slightly in Region 2, and remained stable in all other regions in Week 20 compared to Week 19. All 10 regions are below their respective baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet remained stable in all age groups in Week 20 compared to Week 19.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 20
(Week ending
May 18, 2024)
Week 19
(Week ending
May 11, 2024)
Week 20
(Week ending
May 18, 2024)
Week 19
(Week ending
May 11, 2024)
Very High0000
High0011
Moderate2031
Low151936
Minimal5250644662
Insufficient Data00262229




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 24,763 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and May 18, 2024. The weekly hospitalization rate observed in Week 20 was 0.2 per 100,000 population. The peak weekly hospitalization rate observed this season was 9.0 per 100,000 population and occurred during Week 52.

Among 24,763 hospitalizations, 20,954 (84.6%) were associated with influenza A virus, 3,631 (14.7%) with influenza B virus, 50 (0.2%) with influenza A virus and influenza B virus co-infection, and 127 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,671 (68.6%) were A(H1N1) pdm09 and 1,683 (31.4%) were A(H3N2).



In these figures, cumulative and weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospitals admissions are subject to reporting delays. As hospitalization data are reviewed each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. Voluntarily reported NHSN hospital data can found at Weekly United States Hospitalization Metrics by Jurisdiction.
Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on May 23, 2024, 0.1% of the deaths that occurred during the week ending May 18, 2024 (Week 20), were due to influenza. This percentage slightly decreased (≥ 0.1 percentage point change) compared to Week 19. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Two influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 20, bringing the total pediatric deaths for this season to 169. One death was associated with an influenza A virus with no subtyping performed and occurred during Week 7 (the week ending February 17, 2024). The other death was associated with an influenza A(H3) virus and occurred during Week 17 (the week ending April 27, 2024).

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated May 31, 2024
fluview-banner2.jpg

Key Updates for Week 21, ending May 25, 2024

Seasonal influenza activity remains low nationally. Viruses


Clinical Lab 1.7%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 1.9%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Map
This week no jurisdictions experienced moderate, high, or very high activity.

FluSurv-NET 0.2 per 100,000


weekly hospitalization rate.

NCHS Mortality 0.1%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 3


influenza-associated deaths were reported this week for a total of 172 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains low nationally.
  • One human infection with an influenza A(H5) virus was reported by the Michigan Department of Health this week. Three human infections with an influenza A(H5) virus have been reported in 2024.
  • CDC estimates that there have been at least 35 million illnesses, 390,000 hospitalizations, and 25,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as flu activity continues.[SUP]2[/SUP]
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Seasonal flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories remained stable (change of ≤0.5 percentage points) compared to the previous week. Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested35,2973,298,461
No. of positive specimens (%)609 (1.7%)345,283 (10.5%)
Positive specimens by type
Influenza A395 (64.9%)237,989 (68.9%)
Influenza B214 (35.1%)107,283 (31.1%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested619109,785
No. of positive specimens5136,456
Positive specimens by type/subtype
Influenza A45 (88.2%)27,736 (76.1%)
Subtyping Performed31 (68.9%)23,425 (84.5%)
(H1N1)pdm0912 (38.7%)15,873 (67.8%)
H3N219 (61.3%)7,552 (32.2%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed14 (31.1%)4,311 (15.5%)
Influenza B6 (11.8%)8,720 (23.9%)
Lineage testing performed2 (33.3%)7,589 (87.0%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage2 (100.0%)7,589 (100.0%)
Lineage not performed4 (66.7%)1,131 (13.0%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Novel Influenza A Virus


A human infection with influenza A(H5) virus was reported by the Michigan Department of Health and Human Services.

The patient, aged >18 years, developed symptoms while working at a commercial dairy farm where highly pathogenic avian influenza (HPAI) A(H5N1) virus has been detected in cows. The patient was referred to the local health department and Michigan Department of Health and Human Services for evaluation and influenza testing. The patient reported congestion, sore throat, cough, fatigue, and “runny” and burning eyes at the time when specimens for influenza testing were collected (including respiratory and conjunctival swabs).

Specimens were tested at the Michigan Public Health Laboratory. The respiratory specimen was presumptive positive for influenza A(H5) virus using a Centers for Disease Control and Prevention (CDC) assay. All specimens were then sent to CDC for further testing. The specimens were received and tested at CDC on May 29, 2024. The respiratory specimen was positive for A(H5) virus using diagnostic RT-PCR. Additional analysis of the respiratory specimen, including genetic sequencing, is underway. The patient was not hospitalized, was provided influenza antivirals per CDC guidance (https://www.cdc.gov/flu/avianflu/clinicians-evaluating-patients.htm), is isolating at home, and symptoms are resolving.

In response to this detection, public health officials are conducting additional case investigation and surveillance activities in the area, including contact tracing of the case. Contacts of the patient have not reported illness and have been offered influenza antiviral post-exposure prophylaxis in accordance with CDC recommendations. Symptom monitoring among workers exposed to infected cattle at the same farm has not identified additional symptomatic persons. Additional cases of human infection with A(H5) virus associated with this case and human-to-human transmission of A(H5) virus have not been identified to date.

This is the fourth person to test positive for A(H5) virus in the United States. The first was reported in April 2022 in Colorado, the second in April 2024 in Texas, and the third was also reported in May 2024 in Michigan. This is the third case associated with an ongoing multistate outbreak of HPAI A(H5N1) in dairy cows and is not linked to the same dairy as the previous Michigan case.

Currently in the United States, HPAI A(H5N1) virus detections among wild birds are widespread. There are outbreaks among animals including poultry, backyard flocks, and dairy cows. Sporadic infections in wild mammals have also been reported by United States Department of Agriculture (USDA) Animal Plant Health Inspection Service (APHIS).

CDC recommends that state and local public health departments monitor people who are exposed to birds or other animals (including livestock) suspected to be infected with avian influenza viruses for onset of signs and symptoms until 10 days after their last exposure and that people who develop signs or symptoms of respiratory illness and/or conjunctivitis be tested for influenza. During February 9, 2022 — May 29, 2024, over 9,400 people were actively monitored following exposure to HPAI infected birds, cows, or other animals.

Interim recommendations for Prevention, Monitoring, and Public Health Investigations are available at https://www.cdc.gov/flu/avianflu/hpai/hpai-interim-recommendations.html.

Information about avian influenza is available at https://www.cdc.gov/flu/avianflu/index.htm.

The latest case reports on avian influenza outbreaks in wild birds, commercial poultry, backyard or hobbyist flocks and mammals, in the United States are available from the USDA at https://www.aphis.usda.gov/aphis/ou...e-information/avian/avian-influenza/2022-hpai.

Additional information regarding human infections with novel influenza A viruses:

Surveillance Methods | FluView Interactive Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 4,653 influenza viruses collected since October 1, 2023.
A/H11,754
6B.1A.5a1,754 (100%)2a406 (23.1%)
2a.11,348 (76.9%)
A/H31,575
3C.2a1b.2a1,575 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,572 (99.8%)
2b1 (0.1%)
B/Victoria1,324
V1A1,324 (100%)3a.21,324 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 398 A(H1N1)pdm09 viruses were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 442 A(H3N2) viruses were antigenically characterized by HI or HINT, and 430 (97.3%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 281 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested4,6391,7541,5721,313
Reduced Inhibition1 (0.02%)1 (0.06%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition3 (0.06%)3 (0.2%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested4,6391,7541,5721,313
Reduced Inhibition2 (0.04%)0 (0.00%)0 (0.00%)2 (0.2%)
Highly Reduced Inhibition3 (0.06%)3 (0.2%)0 (0.00%)0 (0.00%)
ZanamivirViruses Tested4,6391,7541,5721,313
Reduced Inhibition1 (0.02%)0 (0.00%)0 (0.00%)1 (0.08%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested4,5001,6941,5271,279
Decreased Susceptibility1 (0.02%)0 (0.0%)1 (0.07%)0 (0.0%)
Three A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. One B virus had NA-A245G amino acid substitution and showed reduced inhibition by peramivir. One B virus had NA-D197N amino acid substitution and showed reduced inhibition by zanamivir and peramivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, the percentage of visits for respiratory illness that were reported through ILINet remained stable (change of ≤ 0.1 percentage points) compared to the previous week and is below the national baseline. All 10 regions are below their region-specific baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years and 5-24 years age groups and remained stable in all other age groups in Week 21 compared to Week 20.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 21
(Week ending
May 25, 2024)
Week 20
(Week ending
May 18, 2024)
Week 21
(Week ending
May 25, 2024)
Week 20
(Week ending
May 18, 2024)
Very High0000
High0001
Moderate0243
Low211718
Minimal5252644668
Insufficient Data10264239




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 24,889 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and May 25, 2024. The weekly hospitalization rate observed in Week 21 was 0.2 per 100,000 population. The peak weekly hospitalization rate observed this season was 9.0 per 100,000 population and occurred during Week 52.

Among 24,889 hospitalizations, 21,071 (84.7%) were associated with influenza A virus, 3,643 (14.6%) with influenza B virus, 51 (0.2%) with influenza A virus and influenza B virus co-infection, and 124 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,707 (68.4%) were A(H1N1) pdm09 and 1,710 (31.6%) were A(H3N2).



**In this figure, weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospital admissions are subject to reporting delays and are shown as a dashed line for the current season. As hospitalization data are received each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. Voluntarily reported NHSN hospital data can found at Weekly United States Hospitalization Metrics by Jurisdiction.
Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on May 30, 2024, the percentage of deaths that were due to influenza remained stable (< 0.1 percentage point change) compared to the previous week. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Three influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 21, bringing the total pediatric deaths for this season to 172. One death was associated with an influenza A virus with no subtyping performed and occurred during Week 1 (the week ending January 6, 2024). Two deaths occurred during Week 10 (the week ending March 9, 2024); one was associated with an influenza A(H1N1)pdm09 virus and the other was associated with an influenza B virus with no lineage determined.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated June 7, 2024
fluview-banner2.jpg

Key Updates for Week 22, ending June 1, 2024

Seasonal influenza activity remains low nationally. Viruses


Clinical Lab 1.8%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 1.9%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Map
This week no jurisdictions experienced moderate, high, or very high activity.

FluSurv-NET 0.2 per 100,000


weekly hospitalization rate.

NCHS Mortality 0.1%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 1


influenza-associated deaths were reported this week for a total of 173 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains low nationally.
  • CDC estimates that there have been at least 35 million illnesses, 390,000 hospitalizations, and 24,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as flu activity continues.[SUP]2[/SUP]
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Seasonal flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories remained stable (change of ≤0.5 percentage points) compared to the previous week. Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested33,2143,328,139
No. of positive specimens (%)591 (1.8%)346,143 (10.4%)
Positive specimens by type
Influenza A435 (73.6%)238,589 (68.9%)
Influenza B156 (26.4%)107,543 (31.1%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested710111,201
No. of positive specimens7736,837
Positive specimens by type/subtype
Influenza A51 (66.2%)28,029 (76.1%)
Subtyping Performed36 (70.6%)23,619 (84.3%)
(H1N1)pdm0915 (41.7%)15,979 (67.7%)
H3N221 (58.3%)7,640 (32.3%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed15 (29.4%)4,410 (15.7%)
Influenza B26 (33.8%)8,808 (23.9%)
Lineage testing performed22 (84.6%)7,669 (87.1%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage22 (100.0%)7,669 (100.0%)
Lineage not performed4 (15.4%)1,139 (12.9%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 4,722 influenza viruses collected since October 1, 2023.
A/H11,770
6B.1A.5a1,770 (100%)2a409 (23.1%)
2a.11,361 (76.9%)
A/H31,602
3C.2a1b.2a1,602 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,599 (99.8%)
2b1 (0.1%)
B/Victoria1,350
V1A1,350 (100%)3a.21,350 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 425 A(H1N1)pdm09 viruses were antigenically characterized by HI, and 424 (99.8%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 442 A(H3N2) viruses were antigenically characterized by HI or HINT, and 430 (97.3%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 302 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested4,6451,7481,5751,321
Reduced Inhibition1 (0.02%)1 (0.1%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition3 (0.1%)3 (0.2%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested4,6451,7481,5751,321
Reduced Inhibition3 (0.1%)0 (0.00%)0 (0.00%)2 (0.2%)
Highly Reduced Inhibition3 (0.1%)3 (0.2%)0 (0.00%)0 (0.00%)
ZanamivirViruses Tested4,6451,7481,5751,321
Reduced Inhibition1 (0.02%)0 (0.00%)0 (0.00%)1 (0.1%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested4,5731,7111,5541,308
Decreased Susceptibility1 (0.02%)0 (0.0%)1 (0.1%)0 (0.0%)
Three A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. Two B viruses had NA-A245G amino acid substitution and showed reduced inhibition by peramivir. One B virus had NA-D197N amino acid substitution and showed reduced inhibition by zanamivir and peramivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, the percentage of visits for respiratory illness that were reported through ILINet remained stable (change of ≤ 0.1 percentage points) compared to the previous week and is below the national baseline. All 10 regions are below their region-specific baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet remained stable for all age groups in Week 22 compared to Week 21.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 22
(Week ending
June 1, 2024)
Week 21
(Week ending
May 25, 2024)
Week 22
(Week ending
June 1, 2024)
Week 21
(Week ending
May 25, 2024)
Very High0000
High0000
Moderate0044
Low232018
Minimal5352653658
Insufficient Data00252249




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 24,976 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and June 1, 2024. The weekly hospitalization rate observed in Week 22 was 0.2 per 100,000 population. The peak weekly hospitalization rate observed this season was 9.0 per 100,000 population and occurred during Week 52.

Among 24,976 hospitalizations, 21,138 (84.6%) were associated with influenza A virus, 3,662 (14.7%) with influenza B virus, 51 (0.2%) with influenza A virus and influenza B virus co-infection, and 125 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,783 (68.5%) were A(H1N1) pdm09 and 1,738 (31.5%) were A(H3N2).



**In this figure, weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospital admissions are subject to reporting delays and are shown as a dashed line for the current season. As hospitalization data are received each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. Voluntarily reported NHSN hospital data can found at Weekly United States Hospitalization Metrics by Jurisdiction.
Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on June 6, 2024, the percentage of deaths that were due to influenza remained stable (< 0.1 percentage point change) compared to the previous week. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


One influenza-associated pediatric death occurring during the 2023-2024 season was reported to CDC during Week 22. The death was associated with an influenza B virus with no lineage determined and occurred during Week 12 (the week ending March 23, 2024).

A total of 173 influenza-associated pediatric deaths occurring during the 2023-2024 season have been reported to CDC.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.

https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated June 14, 2024
fluview-banner2.jpg

Key Updates for Week 23, ending June 8, 2024

Seasonal influenza activity remains low nationally. Viruses


Clinical Lab 1.6%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 1.7%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Map
This week no jurisdictions experienced moderate, high, or very high activity.

FluSurv-NET 0.1 per 100,000


weekly hospitalization rate.

NCHS Mortality 0.1%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 2


influenza-associated deaths were reported this week for a total of 175 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains low nationally.
  • CDC estimates that there have been at least 35 million illnesses, 390,000 hospitalizations, and 25,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as flu activity continues.[SUP]2[/SUP]
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Seasonal flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories remained stable (change of ≤0.5 percentage points) compared to the previous week. Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested31,8243,391,175
No. of positive specimens (%)507 (1.6%)347,368 (10.2%)
Positive specimens by type
Influenza A399 (78.7%)239,625 (69.0%)
Influenza B108 (21.3%)107,732 (31.0%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested626112,317
No. of positive specimens5137,111
Positive specimens by type/subtype
Influenza A41 (80.4%)28,233 (76.1%)
Subtyping Performed26 (63.4%)23,776 (84.2%)
(H1N1)pdm097 (26.9%)16,036 (67.4%)
H3N219 (73.1%)7,740 (32.6%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed15 (36.6%)4,457 (15.8%)
Influenza B10 (19.6%)8,878 (23.9%)
Lineage testing performed9 (90.0%)7,734 (87.1%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage9 (100.0%)7,734 (100.0%)
Lineage not performed1 (10.0%)1,144 (12.9%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 4,824 influenza viruses collected since October 1, 2023.
A/H11,798
6B.1A.5a1,798 (100%)2a417 (23.2%)
2a.11,381 (76.8%)
A/H31,642
3C.2a1b.2a1,642 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,639 (99.8%)
2b1 (0.1%)
B/Victoria1,384
V1A1,384 (100%)3a.21,384 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 425 A(H1N1)pdm09 viruses were antigenically characterized by HI, and 424 (99.8%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 469 A(H3N2) viruses were antigenically characterized by HI or HINT, and 454 (96.8%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 325 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested4,7591,7811,6181,360
Reduced Inhibition1 (0.02%)1 (0.1%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition3 (0.1%)3 (0.2%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested4,7591,7811,6181,360
Reduced Inhibition3 (0.1%)0 (0.00%)0 (0.00%)3 (0.2%)
Highly Reduced Inhibition3 (0.1%)3 (0.2%)0 (0.00%)0 (0.00%)
ZanamivirViruses Tested4,7591,7811,6181,360
Reduced Inhibition1 (0.02%)0 (0.00%)0 (0.00%)1 (0.1%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested4,6811,7401,5941,347
Decreased Susceptibility1 (0.02%)0 (0.0%)1 (0.1%)0 (0.0%)
Three A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. Two B viruses had NA-A245G amino acid substitution and showed reduced inhibition by peramivir. One B virus had NA-D197N amino acid substitution and showed reduced inhibition by zanamivir and peramivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, the percentage of visits for respiratory illness that were reported through ILINet decreased (change of > 0.1 percentage points) compared to the previous week and is below the national baseline. All 10 regions are below their region-specific baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years and 5-24 years age groups and remained stable for all other age groups in Week 23 compared to Week 22.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 23
(Week ending
Jun. 8, 2024)
Week 22
(Week ending
Jun. 1, 2024)
Week 23
(Week ending
Jun. 8, 2024)
Week 22
(Week ending
Jun. 1, 2024)
Very High0000
High0001
Moderate0025
Low02621
Minimal5153627663
Insufficient Data40294239




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 24,970 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and June 8, 2024. The weekly hospitalization rate observed in Week 23 was 0.1 per 100,000 population. The peak weekly hospitalization rate observed this season was 9.0 per 100,000 population and occurred during Week 52.

Among 24,970 hospitalizations, 21,123 (84.6%) were associated with influenza A virus, 3,669 (14.7%) with influenza B virus, 53 (0.2%) with influenza A virus and influenza B virus co-infection, and 125 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,910 (68.5%) were A(H1N1) pdm09 and 1,799 (31.5%) were A(H3N2).



**In this figure, weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospital admissions are subject to reporting delays and are shown as a dashed line for the current season. As hospitalization data are received each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. Voluntarily reported NHSN hospital data can found at Weekly United States Hospitalization Metrics by Jurisdiction.
Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on June 13, 2024, the percentage of deaths that were due to influenza remained stable (< 0.1 percentage point change) compared to the previous week. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Two influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 23. One death was associated with an influenza A virus with no subtyping performed and the other death was associated with an influenza B virus with no lineage determined. Both deaths occurred during Week 12 (the week ending March 23, 2024).

A total of 175 influenza-associated pediatric deaths occurring during the 2023-2024 season have been reported to CDC.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated June 21, 2024
fluview-banner2.jpg

Key Updates for Week 24, ending June 15, 2024

Seasonal influenza activity remains low nationally. Viruses


Clinical Lab 1.4%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 1.6%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Map
This week no jurisdictions experienced moderate, high, or very high activity.

FluSurv-NET 0.1 per 100,000


weekly hospitalization rate.

NCHS Mortality 0.1%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 3


influenza-associated deaths were reported this week for a total of 178 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains low nationally.
  • CDC estimates that there have been at least 35 million illnesses, 390,000 hospitalizations, and 25,000 deaths from flu so far this season.
  • CDC recommends that everyone 6 months and older get an annual flu vaccine as long as flu activity continues.[SUP]2[/SUP]
  • There also are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Seasonal flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories remained stable (change of ≤0.5 percentage points) compared to the previous week. Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested29,1393,415,941
No. of positive specimens (%)416 (1.4%)347,941 (10.2%)
Positive specimens by type
Influenza A325 (78.1%)240,055 (69.0%)
Influenza B91 (21.9%)107,875 (31.0%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested358112,752
No. of positive specimens7837,227
Positive specimens by type/subtype
Influenza A50 (64.1%)28,295 (76.0%)
Subtyping Performed39 (78.0%)23,851 (84.3%)
(H1N1)pdm0913 (33.3%)16,069 (67.4%)
H3N226 (66.7%)7,782 (32.6%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed11 (22.0%)4,444 (15.7%)
Influenza B28 (35.9%)8,932 (24.0%)
Lineage testing performed28 (100.0%)7,790 (87.2%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage28 (100.0%)7,790 (100.0%)
Lineage not performed0 (0.0%)1,142 (12.8%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 4,824 influenza viruses collected since October 1, 2023.
A/H11,817
6B.1A.5a1,817 (100%)2a422 (23.2%)
2a.11,395 (76.8%)
A/H31,659
3C.2a1b.2a1,659 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,656 (99.8%)
2b1 (0.1%)
B/Victoria1,397
V1A1,397 (100%)3a.21,397 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 458 A(H1N1)pdm09 viruses were antigenically characterized by HI, and 457 (99.8%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 509 A(H3N2) viruses were antigenically characterized by HI or HINT, and 492 (96.7%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 342 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested4,7951,7961,6311,368
Reduced Inhibition1 (0.02%)1 (0.1%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition3 (0.1%)3 (0.2%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested4,7951,7961,6311,368
Reduced Inhibition3 (0.1%)0 (0.00%)0 (0.00%)3 (0.2%)
Highly Reduced Inhibition3 (0.1%)3 (0.2%)0 (0.00%)0 (0.00%)
ZanamivirViruses Tested4,7951,7961,6311,368
Reduced Inhibition1 (0.02%)0 (0.00%)0 (0.00%)1 (0.1%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested4,7181,7551,6081,355
Decreased Susceptibility1 (0.02%)0 (0.0%)1 (0.1%)0 (0.0%)
Three A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. Two B viruses had NA-A245G amino acid substitution and showed reduced inhibition by peramivir. One B virus had NA-D197N amino acid substitution and showed reduced inhibition by zanamivir and peramivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, the percentage of visits for respiratory illness that were reported through ILINet remained stable (change of ≤ 0.1 percentage points) compared to the previous week and is below the national baseline. All 10 regions are below their region-specific baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years and 5-24 years age groups and remained stable for all other age groups in Week 24 compared to Week 23.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 24
(Week ending
Jun. 15, 2024)
Week 23
(Week ending
Jun. 8, 2024)
Week 24
(Week ending
Jun. 15, 2024)
Week 23
(Week ending
Jun. 8, 2024)
Very High0000
High0000
Moderate0022
Low1146
Minimal5453670672
Insufficient Data01253249




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 25,015 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and June 15, 2024. The weekly hospitalization rate observed in Week 24 was 0.1 per 100,000 population. The peak weekly hospitalization rate observed this season was 8.9 per 100,000 population and occurred during Week 52.

Among 25,015 hospitalizations, 21,171 (84.6%) were associated with influenza A virus, 3,665 (14.7%) with influenza B virus, 52 (0.2%) with influenza A virus and influenza B virus co-infection, and 126 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 3,982 (68.3%) were A(H1N1) pdm09 and 1,845 (31.7%) were A(H3N2).



**In this figure, weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospital admissions are subject to reporting delays and are shown as a dashed line for the current season. As hospitalization data are received each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. Voluntarily reported NHSN hospital data can found at Weekly United States Hospitalization Metrics by Jurisdiction.
Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on June 20, 2024, the percentage of deaths that were due to influenza remained stable (< 0.1 percentage point change) compared to the previous week. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Three influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 24. Two deaths occurred during Week 11 (the week ending March 16, 2024). One of the deaths was associated with an influenza A(H3) virus and the other was associated with an influenza B/Victoria virus. The third death occurred during Week 21 (the week ending May 25, 2024) and was associated with an influenza B virus with no lineage determined.

A total of 178 influenza-associated pediatric deaths occurring during the 2023-2024 season have been reported to CDC.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.

https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated June 28, 2024
fluview-banner2.jpg

Key Updates for Week 25, ending June 22, 2024

Seasonal influenza activity remains low nationally. Viruses


Clinical Lab 1.1%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 1.5%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Map
This week no jurisdictions experienced moderate, high, or very high activity.

FluSurv-NET 0.2 per 100,000


weekly hospitalization rate.

NCHS Mortality 0.1%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 3


influenza-associated deaths were reported this week for a total of 181 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains low nationally.
  • CDC estimates that there have been at least 35 million illnesses, 390,000 hospitalizations, and 25,000 deaths from flu so far this season.
  • There are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Seasonal flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories remained stable (change of ≤0.5 percentage points) compared to the previous week. Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested31,8543,457,891
No. of positive specimens (%)352 (1.1%)348,428 (10.1%)
Positive specimens by type
Influenza A283 (80.4%)240,427 (69.0%)
Influenza B69 (19.6%)107,990 (31.0%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested688114,661
No. of positive specimens10137,649
Positive specimens by type/subtype
Influenza A82 (81.2%)28,641 (76.1%)
Subtyping Performed56 (68.3%)24,147 (84.3%)
(H1N1)pdm0921 (37.5%)16,175 (67.0%)
H3N235 (62.5%)7,972 (33.0%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed26 (31.7%)4,494 (15.7%)
Influenza B19 (18.8%)9,008 (23.9%)
Lineage testing performed12 (63.2%)7,853 (87.2%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage12 (100.0%)7,853 (100.0%)
Lineage not performed7 (36.8%)1,155 (12.8%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Novel Influenza A Virus:


Two human infections with a novel influenza A virus were reported by the Pennsylvania Department of Health. The patients, who are close contacts, were both infected with influenza A(H1N2) variant (A(H1N2)v) viruses. Both patients are ≥18 years of age and sought healthcare during the week ending June 22, 2024 (Week 25). One of the patients was hospitalized, and one was not. An investigation by state public health officials found that the patients had attended a livestock auction where swine were present prior to their illness onset. Investigation did not identify illness among additional close contacts of either patient. The investigation is ongoing.

Including these two reports there have been a total of three human infections with variant influenza A viruses reported in the United States in 2024.

When an influenza virus that normally circulates in swine (but not people) is detected in a person, it is called a “variant” influenza virus. Most human infections with variant influenza viruses occur following exposure to swine, but human-to-human transmission can occur. It is important to note that in most cases, variant influenza viruses have not shown the ability to spread easily and sustainably from person to person.

Early identification and investigation of human infections with novel influenza A viruses are critical so that the risk of infection can be understood, and appropriate public health measures can be taken.

Additional information on influenza in swine, variant influenza virus infection in humans, and guidance to interact safely with swine can be found at www.cdc.gov/flu/swineflu/index.htm.

Additional information regarding human infections with novel influenza A viruses:

Surveillance Methods | FluView Interactive Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 4,922 influenza viruses collected since October 1, 2023.
A/H11,828
6B.1A.5a1,828 (100%)2a423 (23.1%)
2a.11,405 (76.9%)
A/H31,681
3C.2a1b.2a1,681 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,678 (99.8%)
2b1 (0.1%)
B/Victoria1,413
V1A1,413 (100%)3a.21,413 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 458 A(H1N1)pdm09 viruses were antigenically characterized by HI, and 457 (99.8%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 537 A(H3N2) viruses were antigenically characterized by HI or HINT, and 519 (96.6%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 342 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested4,8431,8071,6531,383
Reduced Inhibition1 (0.02%)1 (0.1%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition4 (0.1%)4 (0.1%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested4,8431,8071,6531,383
Reduced Inhibition3 (0.1%)0 (0.00%)0 (0.00%)3 (0.2%)
Highly Reduced Inhibition4 (0.1%)4 (0.1%)0 (0.00%)0 (0.00%)
ZanamivirViruses Tested4,8431,8071,6531,383
Reduced Inhibition1 (0.02%)0 (0.00%)0 (0.00%)1 (0.1%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested4,7651,7641,6301,371
Decreased Susceptibility1 (0.02%)0 (0.0%)1 (0.1%)0 (0.0%)
Three A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution and one A(H1N1)pdm09 virus had NA-H275H/Y, conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. Two B viruses had NA-A245G amino acid substitution and showed reduced inhibition by peramivir. One B virus had NA-D197N amino acid substitution and showed reduced inhibition by zanamivir and peramivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, the percentage of visits for respiratory illness that were reported through ILINet remained stable (change of ≤ 0.1 percentage points) compared to the previous week and is below the national baseline. All 10 regions are below their region-specific baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years and 5-24 years age groups and remained stable for all other age groups in Week 25 compared to Week 24.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 25
(Week ending
Jun. 22, 2024)
Week 24
(Week ending
Jun. 15, 2024)
Week 25
(Week ending
Jun. 22, 2024)
Week 24
(Week ending
Jun. 15, 2024)
Very High0000
High0000
Moderate0013
Low1155
Minimal5354676676
Insufficient Data10247245




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 25,155 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and June 22, 2024. The weekly hospitalization rate observed in Week 25 was 0.2 per 100,000 population. The peak weekly hospitalization rate observed this season was 9.0 per 100,000 population and occurred during Week 52.

Among 25,155 hospitalizations, 21,273 (84.6%) were associated with influenza A virus, 3,696 (14.7%) with influenza B virus, 52 (0.2%) with influenza A virus and influenza B virus co-infection, and 133 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 4,112 (67.9%) were A(H1N1) pdm09 and 1,944 (32.1%) were A(H3N2).



**In this figure, weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospital admissions are subject to reporting delays and are shown as a dashed line for the current season. As hospitalization data are received each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. Voluntarily reported NHSN hospital data can found at Weekly United States Hospitalization Metrics by Jurisdiction.
Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on June 27, 2024, the percentage of deaths that were due to influenza remained stable (< 0.1 percentage point change) compared to the previous week. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Three influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 25. Two deaths were associated with influenza A viruses with no subtyping performed. One of the deaths occurred during Week 51 (the week ending December 23, 2023) and the other occurred during Week 14 (the week ending April 6, 2024). The third death occurred during Week 20 (the week ending May 18, 2024) and was associated with an influenza B/Victoria virus.

A total of 181 influenza-associated pediatric deaths occurring during the 2023-2024 season have been reported to CDC.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.
https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated July 5, 2024
fluview-banner2.jpg

Key Updates for Week 26, ending June 29, 2024

Seasonal influenza activity remains low nationally. Viruses


Clinical Lab 1.0%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 1.4%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Map
This week no jurisdictions experienced moderate, high, or very high activity.

FluSurv-NET 0.1 per 100,000


weekly hospitalization rate.

NCHS Mortality 0.02%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 3


influenza-associated deaths were reported this week for a total of 184 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains low nationally.
  • CDC estimates that there have been at least 35 million illnesses, 390,000 hospitalizations, and 25,000 deaths from flu so far this season.
  • There are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Seasonal flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories remained stable (change of ≤0.5 percentage points) compared to the previous week. Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested25,4423,488,352
No. of positive specimens (%)242 (1.0%)348,710 (10.0%)
Positive specimens by type
Influenza A207 (85.5%)240,667 (69.0%)
Influenza B35 (14.5%)108,032 (31.0%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested1,125116,287
No. of positive specimens13637,940
Positive specimens by type/subtype
Influenza A121 (89.0%)28,897 (76.2%)
Subtyping Performed106 (87.6%)24,391 (84.4%)
(H1N1)pdm0933 (31.1%)16,273 (66.7%)
H3N273 (68.9%)8,118 (33.3%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed15 (12.4%)4,506 (15.6%)
Influenza B15 (11.0%)9,043 (23.8%)
Lineage testing performed14 (93.3%)7,890 (87.2%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage14 (100.0%)7,890 (100.0%)
Lineage not performed1 (6.7%)1,153 (12.8%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Novel Influenza A Virus:


A patient aged > 18 years in Colorado developed eye redness and irritation on June 26, 2024, while working at a commercial dairy cattle farm where highly pathogenic avian influenza (HPAI) A(H5N1) virus had been detected in cows. The patient reported their symptoms to the Colorado Department of Public Health and Environment during a public health visit to the farm. Respiratory and conjunctival specimens were collected on June 28, 2024. A respiratory specimen was inconclusive at the Colorado State Public Health Lab using the Centers for Disease Control and Prevention (CDC) influenza A(H5) assay. Specimens were then sent to CDC for further testing. The specimens were received and tested at CDC on July 2, 2024. A respiratory specimen was positive for influenza A and A(H5) virus using diagnostic RT-PCR. Additional analysis of the respiratory specimen, including genetic sequencing, is underway. The patient was not hospitalized, was provided with oseltamivir for treatment and symptoms are resolving.

In response to this detection additional case investigation and surveillance activities are currently ongoing by public health officials.

This is the fifth person to test positive for A(H5) virus in the United States overall. The first was reported in April 2022 in Colorado, the second in April 2024 in Texas, and the third and fourth were reported in May 2024 in Michigan. This is the fourth case associated with an ongoing multistate outbreak of HPAI A(H5N1) in dairy cows in 2024.

Currently in the United States, HPAI A(H5N1) virus has been detected in wild birds, and there have been outbreaks among other animals including commercial poultry, backyard flocks, and dairy cows. Sporadic infections in wild mammals have also been reported by United States Department of Agriculture (USDA) Animal Plant Health Inspection Service (APHIS).

CDC recommends that state and local public health departments monitor people who are exposed to birds or other animals (including livestock) suspected to be infected with avian influenza A viruses for onset of signs and symptoms until 10 days after their last exposure and that people who develop signs or symptoms of respiratory illness and/or conjunctivitis be tested for influenza. During February 9, 2022 — June 29, 2024, over 9,800 people were monitored following exposure to HPAI infected birds, cows, or other animals.

Interim recommendations for Prevention, Monitoring, and Public Health Investigations are available at https://www.cdc.gov/bird-flu/prevention/hpai-interim-recommendations.html.

Information about avian influenza is available at https://www.cdc.gov/flu/avianflu/index.htm.

The latest case reports on avian influenza outbreaks in wild birds, commercial poultry; backyard or hobbyist flocks; and mammals in the United States are available from the USDA at https://www.aphis.usda.gov/aphis/ou...e-information/avian/avian-influenza/2022-hpai.

Additional information regarding human infections with novel influenza A viruses:

Surveillance Methods | FluView Interactive Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 4,922 influenza viruses collected since October 1, 2023.
A/H11,828
6B.1A.5a1,828 (100%)2a423 (23.1%)
2a.11,405 (76.9%)
A/H31,681
3C.2a1b.2a1,681 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,678 (99.8%)
2b1 (0.1%)
B/Victoria1,413
V1A1,413 (100%)3a.21,413 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 476 A(H1N1)pdm09 viruses were antigenically characterized by HI, and 457 (96.0%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 537 A(H3N2) viruses were antigenically characterized by HI or HINT, and 519 (96.6%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 342 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested4,8831,8201,6711,392
Reduced Inhibition1 (0.02%)1 (0.1%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition4 (0.1%)4 (0.2%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested4,8831,8201,6711,392
Reduced Inhibition3 (0.1%)0 (0.00%)0 (0.00%)3 (0.2%)
Highly Reduced Inhibition4 (0.1%)4 (0.2%)0 (0.00%)0 (0.00%)
ZanamivirViruses Tested4,8831,8201,6711,392
Reduced Inhibition1 (0.02%)0 (0.00%)0 (0.00%)1 (0.1%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested4,8031,7751,6481,380
Decreased Susceptibility1 (0.02%)0 (0.0%)1 (0.1%)0 (0.0%)
Three A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution and one A(H1N1)pdm09 virus had NA-H275H/Y, conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. Two B viruses had NA-A245G amino acid substitution and showed reduced inhibition by peramivir. One B virus had NA-D197N amino acid substitution and showed reduced inhibition by zanamivir and peramivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, the percentage of visits for respiratory illness that were reported through ILINet remained stable (change of ≤ 0.1 percentage points) compared to the previous week and is below the national baseline. All 10 regions are below their region-specific baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years age group and remained stable for all other age groups in Week 26 compared to Week 25.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 26
(Week ending
Jun. 29, 2024)
Week 25
(Week ending
Jun. 22, 2024)
Week 26
(Week ending
Jun. 29, 2024)
Week 25
(Week ending
Jun. 22, 2024)
Very High0000
High0001
Moderate0022
Low0065
Minimal5554664679
Insufficient Data01257242




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 25,196 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and June 29, 2024. The weekly hospitalization rate observed in Week 26 was 0.1 per 100,000 population. The peak weekly hospitalization rate observed this season was 9.0 per 100,000 population and occurred during Week 52.

Among 25,196 hospitalizations, 21,301 (84.5%) were associated with influenza A virus, 3,707 (14.7%) with influenza B virus, 53 (0.2%) with influenza A virus and influenza B virus co-infection, and 134(0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 4,223 (68.0%) were A(H1N1) pdm09 and 1,991 (32.0%) were A(H3N2).



**In this figure, weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospital admissions are subject to reporting delays and are shown as a dashed line for the current season. As hospitalization data are received each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. Voluntarily reported NHSN hospital data can found at Weekly United States Hospitalization Metrics by Jurisdiction.
Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on July 3, 2024, the percentage of deaths that were due to influenza slightly decreased (≥0.1 percentage point change) compared to the previous week. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Three influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during Week 26. The deaths occurred during weeks 3, 17 and 18 of 2024 (the weeks ending January 20, April 27, and May 4 of 2024). Two deaths were associated with influenza A viruses and one death was associated with an influenza B virus with no lineage determined. One of the influenza A viruses had subtyping performed and it was an A(H1N1)pdm09 virus.

A total of 184 influenza-associated pediatric deaths occurring during the 2023-2024 season have been reported to CDC.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.

https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated July 12, 2024
fluview-banner2.jpg

Key Updates for Week 27, ending July 6, 2024

Seasonal influenza activity remains low nationally. Viruses


Clinical Lab 0.9%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 1.4%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Map
This week no jurisdictions experienced moderate, high, or very high activity.

FluSurv-NET 0.1 per 100,000


weekly hospitalization rate.

NCHS Mortality 0.1%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 2


influenza-associated deaths were reported this week for a total of 186 deaths this season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains low nationally.
  • CDC estimates that there have been at least 35 million illnesses, 400,000 hospitalizations, and 25,000 deaths from flu so far this season.
  • There are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Seasonal flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories remained stable (change of ≤0.5 percentage points) compared to the previous week. Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested24,5703,546,814
No. of positive specimens (%)223 (0.9%)349,249 (9.8%)
Positive specimens by type
Influenza A207 (92.8%)241,105 (69.0%)
Influenza B16 (7.2%)108,133 (31.0%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested740117,543
No. of positive specimens8338,140
Positive specimens by type/subtype
Influenza A77 (92.8%)29,058 (76.2%)
Subtyping Performed63 (81.8%)24,539 (84.4%)
(H1N1)pdm0914 (22.2%)16,328 (66.5%)
H3N249 (77.8%)8,211 (33.5%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed14 (18.2%)4,519 (15.6%)
Influenza B6 (7.2%)9,082 (23.8%)
Lineage testing performed5 (83.3%)7,899 (87.0%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage5 (100.0%)7,899 (100.0%)
Lineage not performed1 (16.7%)1,183 (13.0%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 5,054 influenza viruses collected since October 1, 2023.
A/H11,865
6B.1A.5a1,865 (100%)2a439 (23.5%)
2a.11,426 (76.5%)
A/H31,745
3C.2a1b.2a1,745 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,742 (99.8%)
2b1 (0.1%)
B/Victoria1,444
V1A1,444 (100%)3a.21,444 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 476 A(H1N1)pdm09 viruses were antigenically characterized by HI, and 475 (99.8%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 555 A(H3N2) viruses were antigenically characterized by HI or HINT, and 535 (96.4%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 377 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested4,9661,8401,7141,412
Reduced Inhibition1 (0.02%)1 (0.05%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition5 (0.10%)5 (0.27%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested4,9661,8401,7141,412
Reduced Inhibition3 (0.06%)0 (0.00%)0 (0.00%)3 (0.21%)
Highly Reduced Inhibition5 (0.10%)5 (0.27%)0 (0.00%)0 (0.00%)
ZanamivirViruses Tested4,9661,8401,7141,412
Reduced Inhibition1 (0.02%)0 (0.00%)0 (0.00%)1 (0.07%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested4,8921,8001,6921,400
Decreased Susceptibility1 (0.02%)0 (0.00%)1 (0.05%)0 (0.00%)
Four A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution and one A(H1N1)pdm09 virus had NA-H275H/Y, conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. Two B viruses had NA-A245G amino acid substitution and showed reduced inhibition by peramivir. One B virus had NA-D197N amino acid substitution and showed reduced inhibition by zanamivir and peramivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, the percentage of visits for respiratory illness that were reported through ILINet remained stable (change of ≤ 0.1 percentage points) compared to the previous week and is below the national baseline. All 10 regions are below their region-specific baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet remained stable for all age groups in Week 27 compared to Week 26.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 27
(Week ending
Jul. 6, 2024)
Week 26
(Week ending
Jun. 29, 2024)
Week 27
(Week ending
Jul. 6, 2024)
Week 26
(Week ending
Jun. 29, 2024)
Very High0000
High0010
Moderate0004
Low0036
Minimal5455664667
Insufficient Data10261252




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 25,251 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and July 6, 2024. The weekly hospitalization rate observed in week 27 was 0.1 per 100,000 population. The peak weekly hospitalization rate observed this season was 9.0 per 100,000 population and occurred during week 52.

Among 25,251 hospitalizations, 21,350 (84.6%) were associated with influenza A virus, 3,716 (14.7%) with influenza B virus, 53 (0.2%) with influenza A virus and influenza B virus co-infection, and 133 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 4,225 (67.8%) were A(H1N1) pdm09 and 2,001 (32.1%) were A(H3N2).



**In this figure, weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospital admissions are subject to reporting delays and are shown as a dashed line for the current season. As hospitalization data are received each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. Voluntarily reported NHSN hospital data can found at Weekly United States Hospitalization Metrics by Jurisdiction.
Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on July 11, 2024, the percentage of deaths that were due to influenza remained stable (<0.1 percentage point change) compared to the previous week. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Two influenza-associated pediatric deaths occurring during the 2023-2024 season were reported to CDC during week 27. One death was associated with an influenza A(H3) virus and occurred during week 16 (the week ending April 20, 2024). The other death was associated with an influenza B virus with no lineage determined and occurred during week 15 (the week ending April 13, 2024).

A total of 186 influenza-associated pediatric deaths occurring during the 2023-2024 season have been reported to CDC.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.

https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated July 19, 2024
fluview-banner2.jpg

Key Updates for Week 28, ending July 13, 2024

Seasonal influenza activity remains low nationally. Viruses


Clinical Lab 0.8%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 1.4%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Map
This week no jurisdictions experienced moderate, high, or very high activity.

FluSurv-NET 0.1 per 100,000


weekly hospitalization rate.

NCHS Mortality 0.1%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 2


influenza-associated deaths were reported; 1 occurred during 2022-2023 season and 1 occurred during 2023-2024 season.

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains low nationally.
  • CDC estimates that there have been at least 35 million illnesses, 400,000 hospitalizations, and 25,000 deaths from flu so far this season.
  • There are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Seasonal flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories remained stable (change of ≤0.5 percentage points) compared to the previous week. Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested29,8633,578,813
No. of positive specimens (%)236 (0.8%)349,690 (9.8%)
Positive specimens by type
Influenza A206 (87.3%)241,481 (69.1%)
Influenza B30 (12.7%)108,198 (30.9%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested1,010119,075
No. of positive specimens11738,404
Positive specimens by type/subtype
Influenza A113 (96.6%)29,306 (76.3%)
Subtyping Performed95 (84.1%)24,757 (84.5%)
(H1N1)pdm0934 (35.8%)16,417 (66.3%)
H3N261 (64.2%)8,340 (33.7%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed18 (15.9%)4,549 (15.5%)
Influenza B4 (3.4%)9,098 (23.7%)
Lineage testing performed4 (100.0%)7,914 (87.0%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage4 (100.0%)7,914 (100.0%)
Lineage not performed0 (0.0%)1,184 (13.0%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Novel Influenza A Virus:


Five human infections with influenza A(H5) virus were reported by the Colorado Department of Health and Environment.

Five individuals in Colorado, each aged >18 years, tested positive for influenza A(H5) virus. All five had performed disposal and culling operations prior to symptom onset at the same commercial poultry farm where highly pathogenic avian influenza (HPAI) A(H5N1) virus clade 2.3.4.4b, genotype B3.13 had been detected in poultry. All five individuals reported mild symptoms; none were hospitalized; all were offered oseltamivir for treatment; and all are recovering from their illnesses.

All five individuals reported their symptoms to the Colorado Department of Public Health and Environment during daily active monitoring on the farm conducted by public health staff. Specimens were collected from the individuals. Specimens were initially tested at the Colorado State Public Health Laboratory using the Centers for Disease Control and Prevention (CDC) influenza A(H5) assay before being sent to CDC for further testing. The specimens were received and tested at CDC. Specimens from all five individuals were positive for influenza A and A(H5) virus using diagnostic rRT-PCR at CDC. Additional analysis including genetic sequencing is underway.

In response to these detections, additional case investigation and surveillance activities are ongoing by public health officials, including additional specimen collection at this farm from symptomatic individuals. Further symptom screening will continue.

A total of ten people have tested positive for A(H5) virus in the United States since 2022. The first case occurred in April 2022 in Colorado in an individual who had performed poultry culling; the next four occurred in April-June 2024 in individuals who worked with dairy cows in Texas (one case) and Michigan (two cases); followed by these five cases associated with poultry disposal and culling operations in Colorado in July 2024.

Interim recommendations for Prevention, Monitoring, and Public Health Investigations are available at https://www.cdc.gov/bird-flu/prevention/hpai-interim-recommendations.html.

Information about avian influenza is available at https://www.cdc.gov/flu/avianflu/index.htm.

The latest case reports on avian influenza outbreaks in wild birds, commercial poultry; backyard or hobbyist flocks; and mammals in the United States are available from the USDA at https://www.aphis.usda.gov/aphis/ou...e-information/avian/avian-influenza/2022-hpai.

Additional information regarding human infections with novel influenza A viruses:

Surveillance Methods | FluView Interactive Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 5,077 influenza viruses collected since October 1, 2023.
A/H11,872
6B.1A.5a1,872 (100%)2a443 (23.7%)
2a.11,429 (76.3%)
A/H31,755
3C.2a1b.2a1,755 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,752 (99.8%)
2b1 (0.1%)
B/Victoria1,450
V1A1,450 (100%)3a.21,450 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 494 A(H1N1)pdm09 viruses were antigenically characterized by HI, and 493 (99.8%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 555 A(H3N2) viruses were antigenically characterized by HI or HINT, and 535 (96.4%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 400 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested4,9901,8471,7241,419
Reduced Inhibition1 (0.02%)1 (0.1%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition5 (0.1%)5 (0.3%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested4,9901,8471,7241419
Reduced Inhibition3 (0.1%)0 (0.00%)0 (0.00%)3 (0.2%)
Highly Reduced Inhibition6 (0.1%)5 (0.3%)0 (0.00%)1 (0.1%)
ZanamivirViruses Tested4,9901,8471,7241,419
Reduced Inhibition1 (0.02%)0 (0.00%)0 (0.00%)1 (0.1%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested4,9151,8071,7031,405
Decreased Susceptibility1 (0.02%)0 (0.00%)1 (0.1%)0 (0.00%)
Four A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution and one A(H1N1)pdm09 virus had NA-H275H/Y, conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. Two B viruses had NA-A245G amino acid substitution and showed reduced inhibition by peramivir. One B virus had NA-D197N amino acid substitution and showed reduced inhibition by zanamivir and peramivir. One B virus had NA-H273Y amino acid substitution and showed highly reduced inhibition by zanamivir and peramivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, the percentage of visits for respiratory illness that were reported through ILINet remained stable (change of ≤ 0.1 percentage points) compared to the previous week and is below the national baseline. All 10 regions are below their region-specific baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years age group and remained stable for all other age groups in Week 28 compared to Week 27.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 28
(Week ending
Jul. 13, 2024)
Week 27
(Week ending
Jul. 6, 2024)
Week 28
(Week ending
Jul. 13, 2024)
Week 27
(Week ending
Jul. 6, 2024)
Very High0000
High0011
Moderate0010
Low1033
Minimal5454664677
Insufficient Data01260248




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 25,274 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and July 13, 2024. The weekly hospitalization rate observed in Week 28 was 0.1 per 100,000 population. The peak weekly hospitalization rate observed this season was 9.0 per 100,000 population and occurred during Week 52.

Among 25,274 hospitalizations, 21,371 (84.6%) were associated with influenza A virus, 3,720 (14.7%) with influenza B virus, 52 (0.2%) with influenza A virus and influenza B virus co-infection, and 131 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 4,238 (67.8%) were A(H1N1) pdm09 and 2,009 (32.2%) were A(H3N2).



**In this figure, weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospital admissions are subject to reporting delays and are shown as a dashed line for the current season. As hospitalization data are received each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. Voluntarily reported NHSN hospital data can found at Weekly United States Hospitalization Metrics by Jurisdiction.
Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on July 18, 2024, the percentage of deaths that were due to influenza remained stable (<0.1 percentage point change) compared to the previous week. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


Two influenza-associated pediatric deaths were reported to CDC during Week 28.

One death occurred during Week 15 of the 2023-2024 season (the week ending April 13, 2024), bringing the total pediatric deaths for this season to 187. The other death occurred during Week 22 of the 2022-2023 season (the week ending June 3, 2023), which brings the total number of pediatric deaths for last season to 186. Both deaths were associated with an influenza B virus with no lineage determined.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.

https://www.cdc.gov/flu/weekly/index.htm
 
Weekly U.S. Influenza Surveillance Report


Print
Updated July 26, 2024
fluview-banner2.jpg

Key Updates for Week 29, ending July 20, 2024

Seasonal influenza activity remains low nationally. Viruses


Clinical Lab 0.7%

(Trend )


positive for influenza
this week


Public Health Lab
Influenza A(H1N1)pdm09, A(H3N2), and B viruses were all co-circulating this week.

Virus Characterization
Genetic and antigenic characterization and antiviral susceptibility are summarized in this report. Illness


Outpatient Respiratory Illness 1.4%

(Trend )


of visits to a health care provider this week were for respiratory illness
(below baseline).


Outpatient Respiratory Illness: Map
This week, no jurisdictions experienced moderate, high, or very high activity.

FluSurv-NET 0.1 per 100,000


weekly hospitalization rate.

NCHS Mortality 0.04%

(Trend )


of deaths attributed to influenza this week.

Pediatric Deaths 0


influenza-associated deaths reported this week

All data are preliminary and may change as more reports are received.

Directional arrows indicate changes between the current week and the previous week. Additional information on the arrows can be found at the bottom of this page.

A description of the CDC influenza surveillance system, including methodology and detailed descriptions of each data component is available on the surveillance methods page.

Additional information on the current and previous influenza seasons for each surveillance component are available on FluView Interactive.

Key Points
  • Seasonal influenza activity remains low nationally.
  • Four additional human infections with an influenza A(H5) virus were reported by the Colorado Department of Public Health and Environment.
  • CDC estimates that there have been at least 35 million illnesses, 400,000 hospitalizations, and 25,000 deaths from flu so far this season.
  • There are prescription flu antiviral drugs that can treat flu illness; those should be started as early as possible and are especially important for higher risk patients.[SUP]3[/SUP]
  • Seasonal flu viruses are among several viruses contributing to respiratory disease activity. CDC is providing updated, integrated information about COVID-19, flu, and RSV activity on a weekly basis.
U.S. Virologic Surveillance


Nationally, the percentage of respiratory specimens testing positive for influenza in clinical laboratories remained stable (change of ≤0.5 percentage points) compared to the previous week. Nationally, influenza A(H1N1)pdm09, A(H3N2), and B/Victoria viruses are all co-circulating. However, the distribution of circulating viruses varies by region. For regional and state level data and age group distribution, please visit FluView Interactive. Clinical Laboratories


The results of tests performed by clinical laboratories nationwide are summarized below. Data from clinical laboratories (the percentage of specimens tested that are positive for influenza virus) are used to monitor whether influenza activity is increasing or decreasing.
No. of specimens tested29,2203,616,901
No. of positive specimens (%)195 (0.7%)350,001 (9.7%)
Positive specimens by type
Influenza A174 (89.2%)241,761 (69.1%)
Influenza B21 (10.8%)108,229 (30.9%)
Public Health Laboratories


The results of tests performed by public health laboratories nationwide are summarized below. Data from public health laboratories are used to monitor the proportion of circulating influenza viruses that belong to each influenza subtype/lineage.
No. of specimens tested935120,400
No. of positive specimens8138,579
Positive specimens by type/subtype
Influenza A76 (93.8%)29,474 (76.4%)
Subtyping Performed62 (81.6%)24,917 (84.5%)
(H1N1)pdm0923 (37.1%)16,474 (66.1%)
H3N239 (62.9%)8,443 (33.9%)
H3N2v0 (0.0%)0 (0.0%)
Subtyping not performed14 (18.4%)4,557 (15.5%)
Influenza B5 (6.2%)9,104 (23.6%)
Lineage testing performed5 (100.0%)7,922 (87.0%)
Yamagata lineage0 (0.0%)0 (0.0%)
Victoria lineage5 (100.0%)7,922 (100.0%)
Lineage not performed0 (0.0%)1,182 (13.0%)

Additional virologic surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or Age Data Novel Influenza A Virus:


Four additional human infections with an influenza A(H5) virus were reported by the Colorado Department of Public Health and Environment.

Four individuals in Colorado, all aged >18 years, have tested positive for influenza A(H5) virus infection. All four individuals had performed disposal and culling operations prior to symptom onset at one of two Colorado poultry facilities where highly pathogenic avian influenza (HPAI) A(H5N1) virus clade 2.3.4.4b, genotype B3.13, was detected in poultry.

All four individuals reported their symptoms to the Colorado Department of Public Health and Environment during regular active monitoring on the farm conducted by public health staff. Specimens were collected from the individuals. Specimens were initially tested at the Colorado State Public Health Laboratory using the Centers for Disease Control and Prevention (CDC) influenza A(H5) assay before being sent to CDC for further testing. Specimens from all four individuals were positive for influenza A and A(H5) virus using diagnostic rRT-PCR at CDC. Additional analysis including genetic sequencing is underway.

In response to these detections, additional case investigations and surveillance activities are being conducted by public health officials, including the collection of additional specimens from symptomatic individuals at these farms. Further symptom screening will also continue.

A total of 14 people have tested positive for influenza A(H5) virus in the United States since 2022. The first case occurred in April 2022 in Colorado in an individual who had performed poultry culling. The next four cases occurred April-June 2024 in Texas (one case), Michigan (two cases), and Colorado (one case) in individuals who worked with dairy cows, followed by nine cases in persons associated with poultry disposal and culling operations in Colorado in July 2024.

Interim recommendations for Prevention, Monitoring, and Public Health Investigations are available at https://www.cdc.gov/bird-flu/prevention/hpai-interim-recommendations.html.

Information about avian influenza is available at https://www.cdc.gov/flu/avianflu/index.htm.

The latest case reports on avian influenza outbreaks in wild birds, commercial poultry; backyard or hobbyist flocks; and mammals in the United States are available from the USDA at https://www.aphis.usda.gov/aphis/ou...e-information/avian/avian-influenza/2022-hpai.

Additional information regarding human infections with novel influenza A viruses:

Surveillance Methods | FluView Interactive Influenza Virus Characterization


CDC performs genetic and antigenic characterization of U.S. viruses submitted from state and local public health laboratories according to the Right Size Roadmap submission guidance. These data are used to compare how similar the currently circulating influenza viruses are to the reference viruses representing viruses contained in the current influenza vaccines. The data are also used to monitor evolutionary changes that continually occur in influenza viruses circulating in humans. CDC also tests susceptibility of circulating influenza viruses to antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir.

CDC has genetically characterized 5,077 influenza viruses collected since October 1, 2023.
A/H11,890
6B.1A.5a1,890 (100%)2a451 (23.9%)
2a.11,439 (76.1%)
A/H31,775
3C.2a1b.2a1,775 (100%)2a.1b1 (0.1%)
2a.3a1 (0.1%)
2a.3a.11,772 (99.8%)
2b1 (0.1%)
B/Victoria1,462
V1A1,462 (100%)3a.21,462 (100%)
B/Yamagata0
Y30Y30 (0%)
CDC antigenically characterizes influenza viruses by hemagglutination inhibition (HI) (H1N1pdm09, H3N2, B/Victoria, and B/Yamagata viruses) or neutralization-based HINT (H3N2 viruses) using antisera that ferrets make after being infected with reference viruses representing the 2023-2024 Northern Hemisphere recommended cell or recombinant-based vaccine viruses. Antigenic differences between viruses are determined by comparing how well the antibodies made against the vaccine reference viruses recognize the circulating viruses that have been grown in cell culture. Ferret antisera are useful because antibodies raised against a particular virus can often recognize small changes in the surface proteins of other viruses. In HI assays, viruses with similar antigenic properties have antibody titer differences of less than or equal to 4-fold when compared to the reference (vaccine) virus. In HINT, viruses with similar antigenic properties have antibody neutralization titer differences of less than or equal to 8-fold. Viruses selected for antigenic characterization are a subset representing the genetic changes in the surface proteins seen in genetically characterized viruses.

Influenza A Viruses
  • A (H1N1)pdm09: 494 A(H1N1)pdm09 viruses were antigenically characterized by HI, and 493 (99.8%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown A/Wisconsin/67/2022-like reference viruses representing the A(H1N1)pdm09 component for the cell- and recombinant-based influenza vaccines.
  • A (H3N2): 581 A(H3N2) viruses were antigenically characterized by HI or HINT, and 558 (96.0%) were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer in HI or reacting at titers that were less than or equal to 8-fold of the homologous virus in HINT) by ferret antisera to cell-grown A/Darwin/6/2021-like reference viruses representing the A(H3N2) component for the cell- and recombinant-based influenza vaccines.
Influenza B Viruses
  • B/Victoria: 400 influenza B/Victoria-lineage virus were antigenically characterized by HI, and all were well-recognized (reacting at titers that were within 4-fold of the homologous virus titer) by ferret antisera to cell-grown B/Austria/1359417/2021-like reference viruses representing the B/Victoria component for the cell- and recombinant-based influenza vaccines.
  • B/Yamagata: No influenza B/Yamagata-lineage viruses were available for antigenic characterization.
Assessment of Virus Susceptibility to Antiviral Medications

CDC assesses susceptibility of influenza viruses to the antiviral medications including the neuraminidase inhibitors (oseltamivir, zanamivir, and peramivir) and the PA endonuclease inhibitor baloxavir using next generation sequence analysis supplemented by laboratory assays. Information about antiviral susceptibility test methods can be found at U.S. Influenza Surveillance: Purpose and Methods | CDC.

Viruses collected in the U.S. since October 1, 2023, were tested for antiviral susceptibility as follows:
Neuraminidase InhibitorsOseltamivirViruses Tested5,0371,8641,7441,429
Reduced Inhibition1 (0.02%)1 (0.1%)0 (0.00%)0 (0.00%)
Highly Reduced Inhibition5 (0.1%)5 (0.3%)0 (0.00%)0 (0.00%)
PeramivirViruses Tested5,0371,8641,7441,429
Reduced Inhibition3 (0.1%)0 (0.00%)0 (0.00%)3 (0.2%)
Highly Reduced Inhibition6 (0.1%)5 (0.3%)0 (0.00%)1 (0.1%)
ZanamivirViruses Tested5,0371,8641,7441,429
Reduced Inhibition1 (0.02%)0 (0.00%)0 (0.00%)1 (0.1%)
Highly Reduced Inhibition0 (0.00%)0 (0.00%)0 (0.00%)0 (0.00%)
PA Cap-Dependent Endonuclease InhibitorBaloxavirViruses Tested4,9601,8201,7231,417
Decreased Susceptibility1 (0.02%)0 (0.00%)1 (0.1%)0 (0.00%)
Four A(H1N1)pdm09 viruses had NA-H275Y amino acid substitution and one A(H1N1)pdm09 virus had NA-H275Y/H, conferring highly reduced inhibition by oseltamivir and peramivir. One (H1N1)pdm09 virus had NA-I223V and NA-S247N amino acid substitutions and showed reduced inhibition by oseltamivir. Two B viruses had NA-A245G amino acid substitution and showed reduced inhibition by peramivir. One B virus had NA-D197N amino acid substitution and showed reduced inhibition by zanamivir and peramivir. One B virus had NA-H273Y amino acid substitution and showed highly reduced inhibition by peramivir. One A(H3N2) virus had PA-I38T amino acid substitution and showed reduced susceptibility to baloxavir.

High levels of resistance to the adamantanes (amantadine and rimantadine) persist among influenza A(H1N1)pdm09 and influenza A(H3N2) viruses (the adamantanes are not effective against influenza B viruses). Therefore, use of these antivirals for treatment and prevention of influenza A virus infection is not recommended and data from adamantane resistance testing are not presented. Outpatient Respiratory Illness Surveillance


The U.S. Outpatient Influenza-like Illness Surveillance Network (ILINet) monitors outpatient visits for respiratory illness referred to as influenza-like illness [ILI (fever plus cough or sore throat)], not laboratory-confirmed influenza and will therefore capture respiratory illness visits due to infection with pathogens that can present with similar symptoms, including influenza viruses, SARS-CoV-2, and RSV. It is important to evaluate syndromic surveillance data, including that from ILINet, in the context of other sources of surveillance data to obtain a more complete and accurate picture of influenza, SARS-CoV-2, and other respiratory virus activity. CDC is providing integrated information about COVID-19, influenza, and RSV activity on a website that is updated weekly. Information about other respiratory virus activity can be found on CDC’s National Respiratory and Enteric Virus Surveillance System (NREVSS) website. Outpatient Respiratory Illness Visits


Nationally, the percentage of visits for respiratory illness that were reported through ILINet remained stable (change of ≤ 0.1 percentage points) compared to the previous week and is below the national baseline. All 10 regions are below their region-specific baselines. Multiple respiratory viruses are co-circulating, and the relative contribution of influenza virus infection to ILI varies by location.

Outpatient Respiratory Illness Visits by Age Group


About 70% of ILINet participants provide both the number of patient visits for respiratory illness and the total number of patient visits for the week broken out by age group. Data from this subset of providers are used to calculate the percentages of patient visits for respiratory illness by age group.

The percentage of visits for respiratory illness reported in ILINet decreased in the 0-4 years age group and remained stable for all other age groups in Week 29 compared to Week 28.

Outpatient Respiratory Illness Activity Map


Data collected in ILINet are used to produce a measure of ILI activity* by state/jurisdiction and Core Based Statistical Areas (CBSA).
Week 29
(Week ending
Jul. 20, 2024)
Week 28
(Week ending
Jul. 13, 2024)
Week 29
(Week ending
Jul. 20, 2024)
Week 28
(Week ending
Jul. 13, 2024)
Very High0000
High0001
Moderate0022
Low0052
Minimal5555663668
Insufficient Data00259256




*Data collected in ILINet may disproportionally represent certain populations within a jurisdiction or CBSA, and therefore, may not accurately depict the full picture of influenza activity for the entire jurisdiction or CBSA. Differences in the data presented here by CDC and independently by some health departments likely represent differing levels of data completeness with data presented by the health department likely being the more complete.
Additional information about medically attended visits for ILI for current and past seasons:
Surveillance Methods | FluView Interactive: National, Regional, and State Data or ILI Activity Map Hospitalization Surveillance

FluSurv-NET


The Influenza Hospitalization Surveillance Network (FluSurv-NET) conducts population-based surveillance for laboratory-confirmed influenza-related hospitalizations in select counties in 14 states and represents approximately 9% of the U.S. population. FluSurv-NET hospitalization data are preliminary. As data are received each week, prior case counts and rates are updated accordingly.

A total of 25,279 laboratory-confirmed influenza-associated hospitalizations were reported by FluSurv-NET sites between October 1, 2023, and July 20, 2024. The weekly hospitalization rate observed in Week 29 was 0.1 per 100,000 population. The peak weekly hospitalization rate observed this season was 9.0 per 100,000 population and occurred during Week 52.

Among 25,279 hospitalizations, 21,376 (84.6%) were associated with influenza A virus, 3,721 (14.7%) with influenza B virus, 51 (0.2%) with influenza A virus and influenza B virus co-infection, and 131 (0.5%) with influenza virus for which the type was not determined. Among those with influenza A subtype information, 4,241 (67.9%) were A(H1N1) pdm09 and 2,009 (32.1%) were A(H3N2).



**In this figure, weekly rates for all seasons prior to the 2023-2024 season reflect end-of-season rates. For the 2023-2024 season, rates for recent hospital admissions are subject to reporting delays and are shown as a dashed line for the current season. As hospitalization data are received each week, prior case counts and rates are updated accordingly.
Additional FluSurv-NET hospitalization surveillance information for current and past seasons and additional age groups:
Surveillance Methods |FluView Interactive: Rates by Age, Sex, and Race/Ethnicity or Data on Patient Characteristics | RESP-NET Interactive National Healthcare Safety Network (NHSN) Hospitalization Surveillance


Effective May 1, 2024, hospitals are no longer required to report hospital admissions, hospital capacity, or hospital occupancy data to HHS through NHSN. Voluntarily reported NHSN hospital data can found at Weekly United States Hospitalization Metrics by Jurisdiction.
Additional NHSN Hospitalization Surveillance information:
Surveillance Methods | Additional Data | FluView Interactive Mortality Surveillance

National Center for Health Statistics (NCHS) Mortality Surveillance


Based on NCHS mortality surveillance data available on July 25, 2024, the percentage of deaths that were due to influenza remained stable (<0.1 percentage point change) compared to the previous week. The data presented are preliminary and may change as more data are received and processed.

Additional pneumonia, influenza and COVID-19 mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Influenza-Associated Pediatric Mortality


No influenza-associated pediatric deaths were reported to CDC during Week 29.

A total of 187 influenza-associated pediatric deaths occurring during the 2023-2024 season have been reported to CDC.

Additional pediatric mortality surveillance information for current and past seasons:
Surveillance Methods | FluView Interactive Trend Indicators


Increasing:
IncreasingArrow.png

Decreasing:
DecreasingArrow.png

Stable:
StableArrow.png
Indicators Status by System


Clinical Labs: Up or down arrows indicate a change of greater than or equal to 0.5 percentage points in the percent of specimens positive for influenza compared to the previous week.
Outpatient Respiratory Illness (ILINet): Up or down arrows indicate a change of greater than 0.1 percentage points in the percent of visits due to respiratory illness (ILI) compared to the previous week.
NHSN Hospitalizations: Up or down arrows indicate change of greater than or equal to 5% of the number of patients admitted with laboratory-confirmed influenza compared to the previous week.
NCHS Mortality: Up or down arrows indicate change of greater than 0.1 percentage points of the percent of deaths due to influenza compared to the previous week. Reference Footnotes


[SUP]1[/SUP]U.S. Influenza Surveillance: Purpose and Methods (2023 Oct). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/weekly/overview.htm#ILINet.

[SUP]2[/SUP]Grohskopf LA, Blanton LH, Ferdinands JM, Chung JR, Broder KR, Talbot HK. Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices — United States, 2023–24 Influenza Season. MMWR Recomm Rep 2023;72(No. RR-2):1–25. DOI: http://dx.doi.org/10.15585/mmwr.rr7202a1

[SUP]3[/SUP]Influenza Antiviral Medications: Summary for Clinicians (2023 Sept). Centers for Disease Control and Prevention. https://www.cdc.gov/flu/professionals/antivirals/summary-clinicians.htm.

Additional National and International Influenza Surveillance Information


FluView Interactive: FluView includes enhanced web-based interactive applications that can provide dynamic visuals of the influenza data collected and analyzed by CDC. These FluView Interactive applications allow people to create customized, visual interpretations of influenza data, as well as make comparisons across flu seasons, regions, age groups and a variety of other demographics.

National Institute for Occupational Safety and Health: Monthly surveillance data on the prevalence of health-related workplace absenteeism among full-time workers in the United States are available from NIOSH.

https://www.cdc.gov/flu/weekly/index.htm
 
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