Evidence map›Paper›PMID 35169811›Full record

ArticlemedRxiv : the preprint server for health sciences2022

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 Talbot, Jonathan D Casey and 50 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 32 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

60 authors at 20 institutions in 1 country.

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
Influenza and Other Viruses in the Acutely Ill (IVY) Network
Vanderbilt University Medical Center · USCDC Foundation · USBaylor Scott & White Health · USUniversity of Michigan · USAlbert Einstein College of Medicine · USHennepin County Medical Center · USJohns Hopkins University · USOregon Health & Science University · USStanford University · USUniversity of California, Los Angeles · USUniversity of Colorado Denver · USUniversity of Iowa · USUniversity of Miami · USUniversity of Utah · USUniversity of Washington · USWake Forest University · USWashington University in St. Louis · USBaystate Medical Center · USBeth Israel Deaconess Medical Center · USCleveland Clinic · US

Funding

Clinical and Translational Training Program in Pulmonary MedicineT32HL087738 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Lorraine B Ware · 2007 to 2026
$7.0M
Anesthesiology Mentored Research TrainingT32GM135169 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI Susan L Ingram, Vesna Jevtovic-Todorovic · 2021 to 2026
$1.0M
NHLBI NIH HHS T32 HL087738NIGMS NIH HHS T32 GM135169
6 · The paper itself

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.

Identifiers

PMID35169811
PMCPMC8845432
OpenAlexW4210915576

What OpenQuestion holds

Textmetadata
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.