Preprint
Clinical Severity and mRNA Vaccine Effectiveness for Omicron, Delta, and Alpha SARS-CoV-2 Variants in the United States: A Prospective Observational Study
medRxiv : the preprint server for health sciences
02/07/2022
DOI: 10.1101/2022.02.06.22270558
PMCID: PMC8845432
PMID: 35169811
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.
Details
- Title: Subtitle
- Clinical Severity and mRNA Vaccine Effectiveness for Omicron, Delta, and Alpha SARS-CoV-2 Variants in the United States: A Prospective Observational Study
- Creators
- Adam S Lauring - University of MichiganMark W Tenforde - Centers for Disease Control and PreventionJames D Chappell - Vanderbilt University Medical CenterManjusha Gaglani - Scott & White HospitalAdit A Ginde - University of Colorado DenverTresa McNeal - Scott & White HospitalShekhar Ghamande - Scott & White HospitalDavid J Douin - University of Colorado DenverH Keipp Talbot - Vanderbilt University Medical CenterJonathan D Casey - Vanderbilt University Medical CenterNicholas M Mohr - University of IowaAnne Zepeski - University of IowaNathan I Shapiro - Beth Israel Deaconess Medical CenterKevin W Gibbs - Wake Forest UniversityD Clark Files - Wake Forest UniversityDavid N Hager - Johns Hopkins MedicineArber Shehu - Johns Hopkins MedicineMatthew E Prekker - Hennepin County Medical CenterHeidi L Erickson - Hennepin County Medical CenterMatthew C Exline - The Ohio State UniversityMichelle N Gong - Albert Einstein College of MedicineAmira Mohamed - Albert Einstein College of MedicineNicholas J JohnsonVasisht Srinivasan - University of WashingtonJay S Steingrub - Baystate Medical CenterIthan D Peltan - Intermountain Medical CenterSamuel M Brown - Intermountain Medical CenterEmily T Martin - University of MichiganArnold S Monto - University of MichiganAkram Khan - Oregon Health & Science UniversityCatherine L Hough - Oregon Health & Science UniversityLaurence W Busse - Emory UniversityCaitlin C Ten LohuisAbhijit Duggal - Cleveland ClinicJennifer G Wilson - Stanford UniversityAlexandra June Gordon - Stanford UniversityNida Qadir - University of California, Los AngelesSteven Y Chang - University of California, Los AngelesChristopher Mallow - University of MiamiCarolina Rivas - University of MiamiHilary M Babcock - Washington University in St. LouisJennie H Kwon - Washington University in St. LouisNatasha Halasa - Vanderbilt University Medical CenterCarlos G Grijalva - Vanderbilt University Medical CenterTodd W Rice - Vanderbilt University Medical CenterWilliam B Stubblefield - Vanderbilt University Medical CenterAdrienne Baughman - Vanderbilt University Medical CenterKelsey N Womack - Vanderbilt University Medical CenterJillian P Rhoads - Vanderbilt University Medical CenterChristopher J Lindsell - Vanderbilt University Medical CenterKimberly W Hart - Vanderbilt University Medical CenterYuwei Zhu - Vanderbilt University Medical CenterKatherine Adams - Centers for Disease Control and PreventionStephanie J Schrag - Centers for Disease Control and PreventionSamantha M Olson - Centers for Disease Control and PreventionMiwako Kobayashi - Centers for Disease Control and PreventionJennifer R Verani - Centers for Disease Control and PreventionManish M Patel - Centers for Disease Control and PreventionWesley H Self - Vanderbilt University Medical Center
- Resource Type
- Preprint
- Publication Details
- medRxiv : the preprint server for health sciences
- DOI
- 10.1101/2022.02.06.22270558
- PMID
- 35169811
- PMCID
- PMC8845432
- Language
- English
- Date posted
- 02/07/2022
- Academic Unit
- Epidemiology; Emergency Medicine; Anesthesia; Injury Prevention Research Center
- Record Identifier
- 9984295919402771
Metrics
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