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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

Authors :
Adam S Lauring
Mark W Tenforde
James D Chappell
Manjusha Gaglani
Adit A Ginde
Tresa McNeal
Shekhar Ghamande
David J Douin
H Keipp Talbot
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
Jennifer 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
Source :
BMJ. :e069761
Publication Year :
2022
Publisher :
BMJ, 2022.

Abstract

ObjectivesTo 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.DesignCase-control study.Setting21 hospitals across the United States.Participants11 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 measuresVaccine 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.ResultsEffectiveness 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).ConclusionsmRNA 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.

Subjects

Subjects :
General Medicine

Details

ISSN :
17561833
Database :
OpenAIRE
Journal :
BMJ
Accession number :
edsair.doi...........fedb6b83ed08c87cee740e32562eb2be
Full Text :
https://doi.org/10.1136/bmj-2021-069761