<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tenforde MW</submitter><funding>National Center for Advancing Translational Sciences</funding><funding>Centers for Disease Control and Prevention</funding><funding>Clinical and Translational Science Award</funding><funding>NIH</funding><funding>NIGMS NIH HHS</funding><pagination>1030-1037</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10226741</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>76(6)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The COVID-19 pandemic was associated with historically low influenza circulation during the 2020-2021 season, followed by an increase in influenza circulation during the 2021-2022 US season. The 2a.2 subgroup of the influenza A(H3N2) 3C.2a1b subclade that predominated was antigenically different from the vaccine strain.&lt;h4>Methods&lt;/h4>To understand the effectiveness of the 2021-2022 vaccine against hospitalized influenza illness, a multistate sentinel surveillance network enrolled adults aged ≥18 years hospitalized with acute respiratory illness and tested for influenza by a molecular assay. Using the test-negative design, vaccine effectiveness (VE) was measured by comparing the odds of current-season influenza vaccination in influenza-positive case-patients and influenza-negative, SARS-CoV-2-negative controls, adjusting for confounders. A separate analysis was performed to illustrate bias introduced by including SARS-CoV-2-positive controls.&lt;h4>Results&lt;/h4>A total of 2334 patients, including 295 influenza cases (47% vaccinated), 1175 influenza- and SARS-CoV-2-negative controls (53% vaccinated), and 864 influenza-negative and SARS-CoV-2-positive controls (49% vaccinated), were analyzed. Influenza VE was 26% (95% CI: -14% to 52%) among adults aged 18-64 years, -3% (-54% to 31%) among adults aged ≥65 years, and 50% (15-71%) among adults aged 18-64 years without immunocompromising conditions. Estimated VE decreased with inclusion of SARS-CoV-2-positive controls.&lt;h4>Conclusions&lt;/h4>During a season where influenza A(H3N2) was antigenically different from the vaccine virus, vaccination was associated with a reduced risk of influenza hospitalization in younger immunocompetent adults. However, vaccination did not provide protection in adults ≥65 years of age. Improvements in vaccines, antivirals, and prevention strategies are warranted.</pubmed_abstract><journal>Clinical infectious diseases : an official publication of the Infectious Diseases Society of America</journal><pubmed_title>Vaccine Effectiveness Against Influenza A(H3N2)-Associated Hospitalized Illness: United States, 2022.</pubmed_title><pmcid>PMC10226741</pmcid><funding_grant_id>UL1 TR002243</funding_grant_id><funding_grant_id>K23 GM129661</funding_grant_id><pubmed_authors>Kwon JH</pubmed_authors><pubmed_authors>Mohr NM</pubmed_authors><pubmed_authors>Exline MC</pubmed_authors><pubmed_authors>Talbot HK</pubmed_authors><pubmed_authors>Chappell JD</pubmed_authors><pubmed_authors>Lindsell CJ</pubmed_authors><pubmed_authors>Baughman A</pubmed_authors><pubmed_authors>Lewis NM</pubmed_authors><pubmed_authors>Gibbs KW</pubmed_authors><pubmed_authors>Gaglani M</pubmed_authors><pubmed_authors>Martin ET</pubmed_authors><pubmed_authors>Tenforde MW</pubmed_authors><pubmed_authors>Hart KW</pubmed_authors><pubmed_authors>Shapiro NI</pubmed_authors><pubmed_authors>Mallow C</pubmed_authors><pubmed_authors>Womack KN</pubmed_authors><pubmed_authors>Self WH</pubmed_authors><pubmed_authors>Patel MM</pubmed_authors><pubmed_authors>Gong MN</pubmed_authors><pubmed_authors>Grijalva CG</pubmed_authors><pubmed_authors>Swan SA</pubmed_authors><pubmed_authors>Halasa N</pubmed_authors><pubmed_authors>Peltan ID</pubmed_authors><pubmed_authors>Steingrub JS</pubmed_authors><pubmed_authors>Adams K</pubmed_authors><pubmed_authors>Influenza and Other Viruses in the Acutely Ill (IVY) Network</pubmed_authors><pubmed_authors>Prekker ME</pubmed_authors><pubmed_authors>Ginde AA</pubmed_authors><pubmed_authors>Lauring AS</pubmed_authors><pubmed_authors>Duggal A</pubmed_authors><pubmed_authors>Hager DN</pubmed_authors></additional><is_claimable>false</is_claimable><name>Vaccine Effectiveness Against Influenza A(H3N2)-Associated Hospitalized Illness: United States, 2022.</name><description>&lt;h4>Background&lt;/h4>The COVID-19 pandemic was associated with historically low influenza circulation during the 2020-2021 season, followed by an increase in influenza circulation during the 2021-2022 US season. The 2a.2 subgroup of the influenza A(H3N2) 3C.2a1b subclade that predominated was antigenically different from the vaccine strain.&lt;h4>Methods&lt;/h4>To understand the effectiveness of the 2021-2022 vaccine against hospitalized influenza illness, a multistate sentinel surveillance network enrolled adults aged ≥18 years hospitalized with acute respiratory illness and tested for influenza by a molecular assay. Using the test-negative design, vaccine effectiveness (VE) was measured by comparing the odds of current-season influenza vaccination in influenza-positive case-patients and influenza-negative, SARS-CoV-2-negative controls, adjusting for confounders. A separate analysis was performed to illustrate bias introduced by including SARS-CoV-2-positive controls.&lt;h4>Results&lt;/h4>A total of 2334 patients, including 295 influenza cases (47% vaccinated), 1175 influenza- and SARS-CoV-2-negative controls (53% vaccinated), and 864 influenza-negative and SARS-CoV-2-positive controls (49% vaccinated), were analyzed. Influenza VE was 26% (95% CI: -14% to 52%) among adults aged 18-64 years, -3% (-54% to 31%) among adults aged ≥65 years, and 50% (15-71%) among adults aged 18-64 years without immunocompromising conditions. Estimated VE decreased with inclusion of SARS-CoV-2-positive controls.&lt;h4>Conclusions&lt;/h4>During a season where influenza A(H3N2) was antigenically different from the vaccine virus, vaccination was associated with a reduced risk of influenza hospitalization in younger immunocompetent adults. However, vaccination did not provide protection in adults ≥65 years of age. Improvements in vaccines, antivirals, and prevention strategies are warranted.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2024-11-09T08:44:50.045Z</modification><creation>2024-11-09T08:44:50.045Z</creation></dates><accession>S-EPMC10226741</accession><cross_references><pubmed>36327388</pubmed><doi>10.1093/cid/ciac869</doi></cross_references></HashMap>