Clinical severity of, and effectiveness of mRNA vaccines against, covid-19 from omicron, delta, and alpha SARS-CoV-2 variants in the United States: prospective observational study

Adam S. Lauring(University of Michigan), Mark W. Tenforde(CDC Foundation), James D. Chappell(Vanderbilt University Medical Center), Manjusha Gaglani(Baylor Scott & White Health), Adit A. Ginde(University of Colorado Denver), Tresa McNeal(Baylor Scott & White Health), Shekhar Ghamande(Baylor Scott & White Health), David J. Douin(University of Colorado Denver), H. Keipp Talbot(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 University), D. Clark Files(Wake Forest University), David N. Hager(Johns Hopkins University), Arber Shehu(Johns Hopkins University), Matthew E. Prekker(Hennepin County Medical Center), Heidi L. Erickson(Hennepin County Medical Center), Matthew C. Exline(The Ohio State University), Michelle N. Gong(Albert Einstein College of Medicine), Amira Mohamed(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(University of Utah), Samuel M. Brown(University of Utah), Emily T. Martin(University of Michigan), Arnold S. Monto(University of Michigan), Akram Khan(Oregon Health & Science University), Catherine L. Hough(Oregon Health & Science University), Laurence W. Busse(Emory University), Caitlin C. ten Lohuis(Emory Healthcare), Abhijit Duggal(Cleveland Clinic), Jennifer G. Wilson(Stanford University), Alexandra June Gordon(Stanford University), 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 in St. Louis), Jennie H. Kwon(Washington University in St. Louis), 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(CDC Foundation), Stephanie J. Schrag(CDC Foundation), Samantha M. Olson(CDC Foundation), Miwako Kobayashi(CDC Foundation), Jennifer R. Verani(CDC Foundation), Manish M. Patel(CDC Foundation), Wesley H. Self(Vanderbilt University Medical Center)
BMJ
March 9, 2022
Cited by 679Open Access
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Abstract

OBJECTIVES: To characterize the clinical severity of covid-19 associated with the alpha, delta, and omicron SARS-CoV-2 variants among adults admitted to hospital and to compare the effectiveness of mRNA vaccines to prevent hospital admissions related to each variant. DESIGN: Case-control study. SETTING: 21 hospitals across the United States. PARTICIPANTS: 11 690 adults (≥18 years) admitted to hospital: 5728 with covid-19 (cases) and 5962 without covid-19 (controls). Patients 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 (11 March to 3 July 2021), delta (4 July to 25 December 2021), and omicron (26 December 2021 to 14 January 2022). MAIN OUTCOME MEASURES: Vaccine effectiveness calculated using a test negative design for mRNA vaccines to prevent covid-19 related hospital admissions by each variant (alpha, delta, omicron). Among patients admitted to hospital with covid-19, disease severity on the World Health Organization's clinical progression scale was compared among variants using proportional odds regression. RESULTS: Effectiveness of the mRNA vaccines to prevent covid-19 associated hospital admissions was 85% (95% confidence interval 82% to 88%) for two vaccine doses against the alpha variant, 85% (83% to 87%) for two doses against the delta variant, 94% (92% to 95%) for three doses against the delta variant, 65% (51% to 75%) for two doses against the omicron variant; and 86% (77% to 91%) for three doses against the omicron variant. In-hospital mortality was 7.6% (81/1060) for alpha, 12.2% (461/3788) for delta, and 7.1% (40/565) for omicron. Among unvaccinated patients with covid-19 admitted to hospital, severity on the WHO clinical progression scale was higher for the delta versus alpha variant (adjusted proportional odds ratio 1.28, 95% confidence interval 1.11 to 1.46), and lower for the omicron versus delta variant (0.61, 0.49 to 0.77). Compared with unvaccinated patients, severity was lower for vaccinated patients for each variant, including alpha (adjusted proportional odds ratio 0.33, 0.23 to 0.49), delta (0.44, 0.37 to 0.51), and omicron (0.61, 0.44 to 0.85). CONCLUSIONS: mRNA vaccines were found to be highly effective in preventing covid-19 associated hospital admissions related to the 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 the delta and alpha variants. Among adults admitted to hospital with covid-19, the omicron variant was associated with less severe disease than the delta variant but still resulted in substantial morbidity and mortality. Vaccinated patients admitted to hospital with covid-19 had significantly lower disease severity than unvaccinated patients for all the variants.


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