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Clinical Severity and mRNA Vaccine Effectiveness for Omicron, Delta, and Alpha SARS-CoV-2 Variants in the United States: A Prospective Observational Study
Adam S. Lauring; Mark W. Tenforde; James D. Chappell; Manjusha Gaglani; Adit A. Ginde; Tresa McNeal; Shekhar Ghamande; David J. Douin; H. Keipp Tablot; Jonathan D. Casey; Nicholas M. Mohr; Anne Zepeski; Nathan I. Shapiro; Kevin W. Gibbs; D. Clark Files; David N. Hager; Arber Shehu; Matthew E. Prekker; Heidi L. Erickson; Matthew C. Exline; Michelle N. Gong; Amira Mohamed; Nicholas J. Johnson; Vasisht Srinivasan; Jay S. Steingrub; Ithan D. Peltan; Samuel M. Brown; Emily T. Martin; Arnold S. Monto; Akram Khan; Catherine L. Hough; Laurence W. Busse; Caitlin C. ten Lohuis; Abhijit Duggal; Jenny G. Wilson; Alexandra June Gordon; Nida Qadir; Steven Y. Chang; Christopher Mallow; Carolina Rivas; Hilary M. Babcock; Jennie H. Kwon; Natasha Halasa; Carlos G. Grijalva; Todd W. Rice; William B. Stubblefield; Adrienne Baughman; Kelsey N. Womack; Jillian P. Rhoads; Christopher J. Lindsell; Kimberly W. Hart; Yuwei Zhu; Katherine Adams; Stephanie J. Schrag; Samantha M. Olson; Miwako Kobayashi; Jennifer R. Verani; Manish M. Patel; Wesley H. Self; - For the Influenza and Other Viruses in the Acutely Ill (IVY) Network.
Affiliation
  • Adam S. Lauring; University of Michigan
  • Mark W. Tenforde; US Centers for Disease Control and Prevention
  • James D. Chappell; Vanderbilt University Medical Center
  • Manjusha Gaglani; Baylor Scott and White Health, Texas A&M University College of Medicine
  • Adit A. Ginde; University of Colorado School of Medicine
  • Tresa McNeal; Baylor Scott and White Health, Texas A&M University College of Medicine
  • Shekhar Ghamande; Baylor Scott and White Health, Texas A&M University College of Medicine
  • David J. Douin; University of Colorado School of Medicine
  • H. Keipp Tablot; Vanderbilt University Medical Center
  • Jonathan D. Casey; Vanderbilt University Medical Center
  • Nicholas M. Mohr; University of Iowa
  • Anne Zepeski; University of Iowa
  • Nathan I. Shapiro; Beth Israel Deaconess Medical Center
  • Kevin W. Gibbs; Wake Forest School of Medicine
  • D. Clark Files; Wake Forest School of Medicine
  • David N. Hager; Johns Hopkins University School of Medicine
  • Arber Shehu; Johns Hopkins University School of Medicine
  • Matthew E. Prekker; Hennepin County Medical Center
  • Heidi L. Erickson; Hennepin County Medical Center
  • Matthew C. Exline; The Ohio State University
  • Michelle N. Gong; Montefiore Health System, Albert Einstein College of Medicine
  • Amira Mohamed; Montefiore Health System, Albert Einstein College of Medicine
  • Nicholas J. Johnson; University of Washington
  • Vasisht Srinivasan; University of Washington
  • Jay S. Steingrub; Baystate Medical Center
  • Ithan D. Peltan; Intermountain Medical Center
  • Samuel M. Brown; Intermountain Medical Center
  • Emily T. Martin; University of Michigan
  • Arnold S. Monto; University of Michigan
  • Akram Khan; Oregon Health and Sciences University
  • Catherine L. Hough; Oregon Health and Sciences University
  • Laurence W. Busse; Emory University
  • Caitlin C. ten Lohuis; Emory University
  • Abhijit Duggal; Cleveland Clinic
  • Jenny G. Wilson; Stanford University School of Medicine
  • Alexandra June Gordon; Stanford University School of Medicine
  • Nida Qadir; University of California-Los Angeles
  • Steven Y. Chang; University of California-Los Angeles
  • Christopher Mallow; University of Miami
  • Carolina Rivas; University of Miami
  • Hilary M. Babcock; Washington University
  • Jennie H. Kwon; Washington University
  • Natasha Halasa; Vanderbilt University Medical Center
  • Carlos G. Grijalva; Vanderbilt University Medical Center
  • Todd W. Rice; Vanderbilt University Medical Center
  • William B. Stubblefield; Vanderbilt University Medical Center
  • Adrienne Baughman; Vanderbilt University Medical Center
  • Kelsey N. Womack; Vanderbilt University Medical Center
  • Jillian P. Rhoads; Vanderbilt University Medical Center
  • Christopher J. Lindsell; Vanderbilt University Medical Center
  • Kimberly W. Hart; Vanderbilt University Medical Center
  • Yuwei Zhu; Vanderbilt University Medical Center
  • Katherine Adams; US Centers for Disease Control and Prevention
  • Stephanie J. Schrag; US Centers for Disease Control and Prevention
  • Samantha M. Olson; US Centers for Disease Control and Prevention
  • Miwako Kobayashi; US Centers for Disease Control and Prevention
  • Jennifer R. Verani; US Centers for Disease Control and Prevention
  • Manish M. Patel; US Centers for Disease Control and Prevention
  • Wesley H. Self; Vanderbilt University Medical Center
  • - For the Influenza and Other Viruses in the Acutely Ill (IVY) Network;
Preprint in English | medRxiv | ID: ppmedrxiv-22270558
ABSTRACT
ObjectivesTo characterize the clinical severity of COVID-19 caused by Omicron, Delta, and Alpha SARS-CoV-2 variants among hospitalized adults and to compare the effectiveness of mRNA COVID-19 vaccines to prevent hospitalizations caused by each variant. DesignA case-control study of 11,690 hospitalized adults. SettingTwenty-one hospitals across the United States. ParticipantsThis study included 5728 cases hospitalized with COVID-19 and 5962 controls hospitalized without COVID-19. Cases were classified into SARS-CoV-2 variant groups based on viral whole genome sequencing, and if sequencing did not reveal a lineage, by the predominant circulating variant at the time of hospital admission Alpha (March 11 to July 3, 2021), Delta (July 4 to December 25, 2021), and Omicron (December 26, 2021 to January 14, 2022). Main Outcome MeasuresVaccine effectiveness was calculated using a test-negative design for COVID-19 mRNA vaccines to prevent COVID-19 hospitalizations by each variant (Alpha, Delta, Omicron). Among hospitalized patients with COVID-19, disease severity on the WHO Clinical Progression Ordinal Scale was compared among variants using proportional odds regression. ResultsVaccine effectiveness of the mRNA vaccines to prevent COVID-19-associated hospitalizations included 85% (95% CI 82 to 88%) for 2 vaccine doses against Alpha; 85% (95% CI 83 to 87%) for 2 doses against Delta; 94% (95% CI 92 to 95%) for 3 doses against Delta; 65% (95% CI 51 to 75%) for 2 doses against Omicron; and 86% (95% CI 77 to 91%) for 3 doses against Omicron. Among hospitalized unvaccinated COVID-19 patients, severity on the WHO Clinical Progression Scale was higher for Delta than Alpha (adjusted proportional odds ratio [aPOR] 1.28, 95% CI 1.11 to 1.46), and lower for Omicron than Delta (aPOR 0.61, 95% CI 0.49 to 0.77). Compared to unvaccinated cases, severity was lower for vaccinated cases for each variant, including Alpha (aPOR 0.33, 95% CI 0.23 to 0.49), Delta (aPOR 0.44, 95% CI 0.37 to 0.51), and Omicron (aPOR 0.61, 95% CI 0.44 to 0.85). ConclusionsmRNA vaccines were highly effective in preventing COVID-19-associated hospitalizations from Alpha, Delta, and Omicron variants, but three vaccine doses were required to achieve protection against Omicron similar to the protection that two doses provided against Delta and Alpha. Among adults hospitalized with COVID-19, Omicron caused less severe disease than Delta, but still resulted in substantial morbidity and mortality. Vaccinated patients hospitalized with COVID-19 had significantly lower disease severity than unvaccinated patients for all the variants.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Experimental_studies / Observational study / Prognostic study / Rct Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Experimental_studies / Observational study / Prognostic study / Rct Language: English Year: 2022 Document type: Preprint
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