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Effectiveness of 2 and 3 mRNA COVID-19 Vaccines Doses against Omicron and Delta-Related Outpatient Illness among Adults, October 2021 - February 2022
Sara Kim; Jessie Chung; Keipp Talbot; Carlos G Grijalva; Karen Wernli; Erika Kiniry; Emily Toth Martin; Arnold Monto; Edward Belongia; Huong Q McLean; Manjusha Gaglani; Mufaddal Mamawala; Mary Patricia Nowalk; Krissy Moehling Geffel; Sara Tartof; Ana Florea; Justin S Lee; Mark W Tenforde; Manish Patel; Brendan Flannery.
Afiliação
  • Sara Kim; Centers for Disease Control and Prevention
  • Jessie Chung; US Centers for Disease Control and Prevention
  • Keipp Talbot; Vanderbilt University Medical Center
  • Carlos G Grijalva; Vanderbilt University Medical Center
  • Karen Wernli; Kaiser Permanente Washington Research Institute
  • Erika Kiniry; Kaiser Permanente Washington Research Institute
  • Emily Toth Martin; University of Michigan-Ann Arbor
  • Arnold Monto; University of Michigan-Ann Arbor
  • Edward Belongia; Marshfield Clinic Research Institute
  • Huong Q McLean; Marshfield Clinic Research Institute
  • Manjusha Gaglani; Baylor Scott and White Health, Texas A&M University College of Medicine
  • Mufaddal Mamawala; Baylor Scott and White Health
  • Mary Patricia Nowalk; University of Pittsburgh
  • Krissy Moehling Geffel; University of Pittsburgh
  • Sara Tartof; Kaiser Permanente Southern California
  • Ana Florea; Kaiser Permanente Southern California
  • Justin S Lee; Centers for Disease Control and Prevention
  • Mark W Tenforde; Centers for Disease Control and Prevention
  • Manish Patel; Centers for Disease Control and Prevention
  • Brendan Flannery; Centers for Disease Control and Prevention
Preprint em Inglês | medRxiv | ID: ppmedrxiv-22273535
ABSTRACT
BackgroundWe estimated SARS-CoV-2 Delta and Omicron-specific effectiveness of 2 and 3 mRNA COVID-19 vaccine doses in adults against symptomatic illness in US outpatient settings. MethodsBetween October 1, 2021, and February 12, 2022, research staff consented and enrolled eligible participants who had fever, cough, or loss of taste or smell and sought outpatient medical care or clinical SARS-CoV-2 testing within 10 days of illness onset. Using the test-negative design, we compared the odds of receiving 2 or 3 mRNA COVID-19 vaccine doses among SARS-CoV-2 cases versus controls using logistic regression. Regression models were adjusted for study site, age, onset week, and prior SARS-CoV-2 infection. Vaccine effectiveness (VE) was calculated as (1 - adjusted odds ratio) x 100%. ResultsAmong 3847 participants included for analysis, 574 (32%) of 1775 tested positive for SARS-CoV-2 during the Delta predominant period and 1006 (56%) of 1794 participants tested positive during the Omicron predominant period. When Delta predominated, VE against symptomatic illness in outpatient settings was 63% (95% CI 51% to 72%) among mRNA 2-dose recipients and 96% (95% CI 93% to 98%) for 3-dose recipients. When Omicron predominated, VE was 21% (95% CI -6% to 41%) among 2-dose recipients and 62% (95% CI 48% to 72%) among 3-dose recipients. ConclusionsIn this adult population, 3 mRNA COVID-19 vaccine doses provided substantial protection against symptomatic illness in outpatient settings when the Omicron variant became the predominant cause of COVID-19 in the U.S. These findings support the recommendation for a 3rd mRNA COVID-19 vaccine dose.
Licença
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Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Estudo observacional / Estudo prognóstico Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Estudo observacional / Estudo prognóstico Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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