• FluTrackers.com Inc. does not provide medical advice. Information on this web site is collected from various internet resources, and the FluTrackers board of directors makes no warranty to the safety, efficacy, correctness or completeness of the information posted on this site by any author or poster. The information collated here is for instructional and/or discussion purposes only and is NOT intended to diagnose or treat any disease, illness, or other medical condition. Every individual reader or poster should seek advice from their personal physician/healthcare practitioner before considering or using any interventions that are discussed on this website. By continuing to access this website you agree to consult your personal physican before using any interventions posted on this website, and you agree to hold harmless FluTrackers.com Inc., the board of directors, the members, and all authors and posters for any effects from use of any medication, supplement, vitamin or other substance, device, intervention, etc. mentioned in posts on this website, or other internet venues referenced in posts on this website.
  • We are not asking for any donations. Do not donate to any entity who says they are raising funds for us.

CIDRAP- NEWS BRIEFS May 21, 2024

Lance

MPH, CSP & CIT Retired, CHMM Emeritus
https://www.cidrap.umn.edu/all-news

New tool may help identify infants at high risk for poor RSV outcomes



News brief

Today at 1:11 p.m.
Mary Van Beusekom, MS
Topics

Respiratory Syncytial Virus (RSV)

A new tool developed by a Vanderbilt University-led team may help identify infants at high risk for severe respiratory syncytial virus (RSV) lower respiratory tract infection (LRTI), according to an abstract presented today at the American Thoracic Society (ATS) 2024 International Conference in San Diego.

"To predict whether these infants developed severe RSV LRTI requiring ICU [intensive care unit] admission during the first year of life, we developed a multivariable logistic regression model," coauthor Tebeb Gebretsadik, MPH, said in an ATS press release. "The model includes demographic and clinical variables collected at or shortly after birth—19 variables in all, such as prenatal smoking, delivery method, maternal age and assisted breathing (ventilation) during birth hospitalization."

The researchers evaluated the tool in infants insured through the Tennessee Medicaid Program, including those who did not receive a preventive monoclonal antibody. They said the tool may be especially helpful during shortages of drugs that help prevent severe RSV, such as nirsevimab (Beyfortus), a monoclonal antibody in short supply in the 2023-24 respiratory virus season.

"At least half of infant hospitalizations due to respiratory syncytial virus (RSV) in the United States are among infants who are currently considered low-risk (i.e., healthy and term)," the study authors said in the abstract.

Tool may persuade vaccine-hesitant parents


Of 429,365 infants, 713 (0.2%) had severe RSV requiring ICU admission. The tool had good predictive accuracy, and internal validation indicated a good fit.

At least half of infant hospitalizations due to respiratory syncytial virus (RSV) in the United States are among infants who are currently considered low-risk (i.e., healthy and term).

Principal investigator Tina Hartert, MD, MPH, said the tool "may also persuade vaccine-hesitant families to accept RSV immunoprophylaxis [vaccination], by showing them their newborn is at high risk."

Coauthor Niek Achten, MD, of Erasmus University in the Netherlands, said it may also prove useful abroad. "In addition to use in the United States during times of limited availability, our tool may prove useful in countries with budgetary constraints needing to prioritize administration to the highest risk infants," he said.

The study was published in Open Forum Infectious Diseases in February. The authors said the tool will undergo validation in other populations and cost-effectiveness and decision-curve analyses.


CARB-X to fund neonatal sepsis vaccine candidate


News brief

Today at 12:02 p.m.
Chris Dall, MA
Topics

Antimicrobial Stewardship

Sepsis
CARB-X today announced an award of $3.96 million to the University of Maryland School of Medicine to develop a vaccine to prevent neonatal sepsis.

The funding from CARB-X (Combating Antibiotic-Resistant Bacteria Biopharmaceutical Accelerator) will help the Center for Vaccine Development and Global Health (CVD) develop a maternal vaccine that targets the surface sugars of Klebsiella pneumoniae, one of the leading causes of neonatal sepsis. The hope is that giving the vaccine to pregnant women will help protect their newborns from infection.

More than 2 million infant deaths a year


An estimated 2.5 million newborns and infants a year die within the first month of life from sepsis, with the greatest burden in low- and middle-income countries. CVD officials say they believe the vaccine, which is being developed in partnership with Auro Vaccines of Hyderabad, India, could prevent 80% to 90% of K pneumoniae neonatal sepsis infections if successful.

"The CVD has participated in research that has highlighted the importance of K. pneumoniae in causing serious infections in young infants in resource limited settings," CVD Interim Director Miriam Laufer, MD, MPH, said in a CARB-X press release. "We are excited to continue development of a vaccine that can prevent these infections and save lives."

The neonatal sepsis vaccine candidate is the second to receive funding through CARB-X's 2022-2023 funding call. In January, the public-private partnership awarded Syntiron of St. Paul, Minnesota, $1.7 million to develop a maternal vaccine targeting neonatal sepsis caused by K pneumoniae and Escherichia coli.

Since its founding in 2016, CARB-X has supported 102 early-stage products for the treatment, diagnosis, and prevention of drug-resistant infections.

ALL BRIEFS
 
Back
Top Bottom