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USA. CDC H1N1 Flu - In The News (11/24/09, edited)

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  • USA. CDC H1N1 Flu - In The News (11/24/09, edited)

    USA. CDC H1N1 Flu - In The News (11/24/09, edited)
    2009 H1N1 Flu In The News - November 24, 2009 6:00 PM ET


    On this Page
    • 2009 H1N1 and Seasonal Influenza Infections and Invasive Pneumococcal Disease
    • 2009 H1N1 Influenza Vaccination Safety
    • Reports of Changes to the 2009 H1N1 Virus
    • 2009 H1N1 Hospitalizations in People with Asthma
    • 2009 H1N1 Hospitalizations by Age Group


    2009 H1N1 and Seasonal Influenza Infections and Invasive Pneumococcal Disease

    Some of CDC's Active Bacterial Core surveillance (ABCs) sites have seen an increase in serious cases of pneumococcal disease coincident with increases in influenza-associated hospitalizations. CDC has been working with state and local public health officials in Colorado for example concerning its ABCs site in the Denver Metro area to collect additional data on pneumococcal disease cases.

    There is good evidence that 2009 H1N1 influenza may be responsible for this increase in invasive pneumococcal disease (IPD) cases in the Denver Metro area. (5-year average number of cases in October, ~20; total number in October 2009, 58).

    The increase in IPD cases in the Denver Metro area is primarily among younger adults with 36 out of 58 (62%) cases occurred among 20-59 year olds. In a typical non-pandemic year, most IPD cases occur among persons 65 years of age and older.

    What occurred in Denver is likely an indicator of what is happening in other parts of the country. Data shown below is preliminary and subject to change upon further investigation.

    For more information on preventing pneumococcal infections secondary to seasonal and 2009 H1N1 influenza: LINK.


    2009 H1N1 Influenza Vaccination Safety

    How many adverse event reports among people who received 2009 H1N1 vaccine have been reported to CDC?

    As of November 20, 2009, the CDC Vaccine Adverse Event Reporting System (VAERS) had received 3,182 adverse event reports following 2009 monovalent H1N1 vaccination. The vast majority (94%) of adverse events reported to VAERS after receiving the 2009 monovalent H1N1 vaccine have not been serious (e.g., they encompass things like soreness at the vaccine injection site). CDC and FDA will be providing weekly updates on our vaccine safety monitoring activities in an effort to better characterize data that are being viewed publicly through the Vaccine Adverse Event Reporting System (VAERS; LINK) and CDC?s website, WONDER (LINK).

    How does 2009 H1N1 vaccine safety compare to seasonal flu vaccine safety?

    The number of serious health events reported after H1N1 vaccination is very similar to the number of reports that typically follow seasonal influenza vaccines. Additionally, no new or unusual events or pattern of adverse events have emerged.

    How many Guillain-Barr? syndrome (GBS) cases have been reported after 2009 H1N1 vaccination?

    We know there has been interest in Guillain-Barr? syndrome (GBS). CDC employs three vaccine monitoring systems that will alert us quickly should any indications of GBS-related issues arise, including: Vaccine Adverse Event Reporting System (VAERS), Vaccine Safety Datalink (VSD), and a collaboration in 10 states to look actively look for cases of GBS regardless of vaccination. To date, there are no indications of GBS-related problems with the 2009 H1N1 vaccine. It is important to note that each week in the United States, about 80-160 cases of GBS occur in the general population - regardless of vaccination. For more information about GBS: LINK.

    How is the government monitoring H1N1 vaccine safety?

    The Federal government has a robust vaccine safety monitoring program that has been enhanced further to ensure 2009 H1N1 vaccine safety. Details available at LINK


    Reports of Changes to the 2009 H1N1 Virus - November 24, 2009 6:00 PM ET

    Have changes to the 2009 H1N1 virus been reported?

    The majority of 2009 H1N1 viruses tested by CDC and the other three World Health Organization (WHO) Collaborating Centres located around the world are similar and have changed relatively little since April 2009 when the 2009 H1N1 virus was first detected. However, there have been occasional reports of small changes in the genes of some virus samples collected from some people infected with 2009 H1N1 in several countries.

    What are these changes to the 2009 H1N1 virus and what are the implications for public health?

    The changes to the 2009 H1N1 virus that have been reported out of Norway, and that WHO has reported as being detected occasionally in viral isolates in other countries, are scientifically known as D222G and D222N changes. The public health implications of these changes are currently being studied by CDC and WHO scientists. At this time, these changes appear to occur sporadically and spontaneously. No links between the small number of patients infected with 2009 H1N1 virus with these changes have been found, and viruses with these changes do not appear to be spreading to other people. Although further investigation is underway, there is no evidence that these changes in the 2009 H1N1 virus have lead to an unusual increase in the number of 2009 H1N1 infections or to a greater number of severe or fatal cases. Worldwide, these changes have been found in mild cases of 2009 H1N1 illness as well as severe cases of illness that have resulted in death. As a result, the public health significance of this finding remains unclear.

    Will the 2009 H1N1 vaccine still protect against these viruses?

    According to CDC and WHO experts, the 2009 H1N1 vaccine remains well matched with the 2009 H1N1 viruses that contain these small changes. There is no reason to think that the 2009 H1N1 vaccine will be less effective against these viruses based on the area of the influenza virus where these changes have occurred.

    Will antiviral drugs work against the 2009 H1N1 viruses that have these changes?

    The D222G and D222N changes found in these 2009 H1N1 isolates are not associated with resistance to oseltamivir or any other influenza antiviral medication.

    Which countries have reported finding 2009 H1N1 viruses with these changes?

    A recent report from the Norwegian Institute of Public Health described a change in the 2009 H1N1 virus (D222G) found in the first two people in Norway who died from 2009 H1N1 as well as an additional Norwegian patient with severe influenza illness. This D222G change was not found in the virus samples isolated from other people who died in Norway of 2009 H1N1 related causes. Norwegian scientists have analyzed samples from more than 70 patients infected with 2009 H1N1, and no additional viral isolates containing these changes have been found.

    In addition to Norway, CDC has received sporadic reports of these changes found in viral isolates from Australia, Brazil, China, Japan, Mexico, Saudi Arabia, Ukraine, Uruguay and the United States.
    (...)
    -
    <cite cite="http://www.cdc.gov/h1n1flu/in_the_news.htm">CDC H1N1 Flu | In The News</cite>

  • #2
    Re: USA. CDC H1N1 Flu - In The News (11/24/09, edited)

    From above: "The vast majority (94&#37 of adverse events reported to VAERS after receiving the 2009 monovalent H1N1 vaccine have not been serious (e.g., they encompass things like soreness at the vaccine injection site)"

    "Among the 177 reports of serious health events, there were 11 reports of death. .
    The 11 VAERS reports that involve deaths are under review by CDC, FDA and the states where the reported deaths occurred. Preliminary findings do not indicate a common cause or pattern
    VAERS has received 10 reports of Guillian-Barr&#233; syndrome (GBS), for which follow-up assessments are underway."
        # 4084     From the VAERS ( Vaccine Adverse Event Reporting System ) we get the latest US pandemic vaccine safety report – d...


    "Each year the VAERS receives 10,000–20,000 reports of adverse events following immunization. Higher-priority uses of the data include reports of death and other serious adverse events, recognizing and detecting adverse effects, and finding unexpected adverse events involving new vaccines."


    "While about 85% of adverse events reported to VAERS are minor (such as mild fevers or redness and swelling at the injection site), the remaining 15% describe more serious events. The more serious events include hospitalizations, life-threatening events, and deaths."
    Last edited by Missouriwatcher; November 27, 2009, 02:48 PM. Reason: additional info

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