Association Between mRNA Vaccination and COVID-19 Hospitalization and Disease Severity

Mark W. Tenforde(CDC Foundation), Wesley H. Self(Vanderbilt University Medical Center), Katherine Adams(CDC Foundation), 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(Montefiore Health System), Amira Mohamed(Montefiore Medical Center), Daniel J. Henning(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–Ann Arbor), Arnold S. Monto(University of Michigan–Ann Arbor), 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), James D. Chappell(Vanderbilt University Medical Center), Adam S. Lauring(University of Michigan–Ann Arbor), Carlos G. Grijalva(Vanderbilt University Medical Center), Todd W. Rice(Vanderbilt University Medical Center), Ian Jones(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), Samantha M. Olson(CDC Foundation), Miwako Kobayashi(CDC Foundation), Jennifer R. Verani(CDC Foundation), Manish M. Patel(CDC Foundation), Influenza and Other Viruses in the Acutely Ill (IVY) Network
JAMA
November 4, 2021
Cited by 681Open Access
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Abstract

Importance: A comprehensive understanding of the benefits of COVID-19 vaccination requires consideration of disease attenuation, determined as whether people who develop COVID-19 despite vaccination have lower disease severity than unvaccinated people. Objective: To evaluate the association between vaccination with mRNA COVID-19 vaccines-mRNA-1273 (Moderna) and BNT162b2 (Pfizer-BioNTech)-and COVID-19 hospitalization, and, among patients hospitalized with COVID-19, the association with progression to critical disease. Design, Setting, and Participants: A US 21-site case-control analysis of 4513 adults hospitalized between March 11 and August 15, 2021, with 28-day outcome data on death and mechanical ventilation available for patients enrolled through July 14, 2021. Date of final follow-up was August 8, 2021. Exposures: COVID-19 vaccination. Main Outcomes and Measures: Associations were evaluated between prior vaccination and (1) hospitalization for COVID-19, in which case patients were those hospitalized for COVID-19 and control patients were those hospitalized for an alternative diagnosis; and (2) disease progression among patients hospitalized for COVID-19, in which cases and controls were COVID-19 patients with and without progression to death or mechanical ventilation, respectively. Associations were measured with multivariable logistic regression. Results: Among 4513 patients (median age, 59 years [IQR, 45-69]; 2202 [48.8%] women; 23.0% non-Hispanic Black individuals, 15.9% Hispanic individuals, and 20.1% with an immunocompromising condition), 1983 were case patients with COVID-19 and 2530 were controls without COVID-19. Unvaccinated patients accounted for 84.2% (1669/1983) of COVID-19 hospitalizations. Hospitalization for COVID-19 was significantly associated with decreased likelihood of vaccination (cases, 15.8%; controls, 54.8%; adjusted OR, 0.15; 95% CI, 0.13-0.18), including for sequenced SARS-CoV-2 Alpha (8.7% vs 51.7%; aOR, 0.10; 95% CI, 0.06-0.16) and Delta variants (21.9% vs 61.8%; aOR, 0.14; 95% CI, 0.10-0.21). This association was stronger for immunocompetent patients (11.2% vs 53.5%; aOR, 0.10; 95% CI, 0.09-0.13) than immunocompromised patients (40.1% vs 58.8%; aOR, 0.49; 95% CI, 0.35-0.69) (P < .001) and weaker at more than 120 days since vaccination with BNT162b2 (5.8% vs 11.5%; aOR, 0.36; 95% CI, 0.27-0.49) than with mRNA-1273 (1.9% vs 8.3%; aOR, 0.15; 95% CI, 0.09-0.23) (P < .001). Among 1197 patients hospitalized with COVID-19, death or invasive mechanical ventilation by day 28 was associated with decreased likelihood of vaccination (12.0% vs 24.7%; aOR, 0.33; 95% CI, 0.19-0.58). Conclusions and Relevance: Vaccination with an mRNA COVID-19 vaccine was significantly less likely among patients with COVID-19 hospitalization and disease progression to death or mechanical ventilation. These findings are consistent with risk reduction among vaccine breakthrough infections compared with absence of vaccination.


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