Impact of Severe Acute Respiratory Syndrome Coronavirus 2 Variants on Inpatient Clinical Outcome

Author:

Robinson Matthew L1ORCID,Morris C Paul23,Betz Joshua F4,Zhang Yifan4,Bollinger Robert1,Wang Natalie5,Thiemann David R6,Fall Amary2,Eldesouki Raghda E2,Norton Julie M2,Gaston David C2,Forman Michael2,Luo Chun Huai2,Zeger Scott L4,Gupta Amita1ORCID,Garibaldi Brian T7,Mostafa Heba H2

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine , Baltimore, Maryland , USA

2. Department of Pathology, Johns Hopkins University School of Medicine , Baltimore, Maryland , USA

3. National Institute of Allergy and Infectious Diseases, National Institutes of Health , Bethesda, Maryland , USA

4. Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health , Baltimore, Maryland , USA

5. Krieger School of Arts & Sciences, Johns Hopkins University , Baltimore, Maryland , USA

6. Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine , Baltimore, Maryland , USA

7. Division of Pulmonary and Critical Care, Department of Medicine, Johns Hopkins University School of Medicine , Baltimore, Maryland , USA

Abstract

Abstract Background Prior observation has shown differences in COVID-19 hospitalization risk between SARS-CoV-2 variants, but limited information describes hospitalization outcomes. Methods Inpatients with COVID-19 at 5 hospitals in the eastern United States were included if they had hypoxia, tachypnea, tachycardia, or fever, and SARS-CoV-2 variant data, determined from whole-genome sequencing or local surveillance inference. Analyses were stratified by history of SARS-CoV-2 vaccination or infection. The average effect of SARS-CoV-2 variant on 28-day risk of severe disease, defined by advanced respiratory support needs, or death was evaluated using models weighted on propensity scores derived from baseline clinical features. Results Severe disease or death within 28 days occurred for 977 (29%) of 3369 unvaccinated patients and 269 (22%) of 1230 patients with history of vaccination or prior SARS-CoV-2 infection. Among unvaccinated patients, the relative risk of severe disease or death for Delta variant compared with ancestral lineages was 1.30 (95% confidence interval [CI]: 1.11–1.49). Compared with Delta, the risk for Omicron patients was .72 (95% CI: .59–.88) and compared with ancestral lineages was .94 (.78–1.1). Among Omicron and Delta infections, patients with history of vaccination or prior SARS-CoV-2 infection had half the risk of severe disease or death (adjusted hazard ratio: .40; 95% CI: .30–.54), but no significant outcome difference by variant. Conclusions Although risk of severe disease or death for unvaccinated inpatients with Omicron was lower than with Delta, it was similar to ancestral lineages. Severe outcomes were less common in vaccinated inpatients, with no difference between Delta and Omicron infections.

Funder

National Institute of Allergy and Infectious Diseases

National Institutes of Health

Johns Hopkins Center of Excellence in Influenza Research and Surveillance

NIH RADx-UP initiative

Centers for Disease Control and Prevention

Maryland Department of Health, the Johns Hopkins University President’s Fund Research Response

the Sherrilyn and Ken Fisher Center for Environmental Infectious Diseases

Scleroderma Research Foundation Trajectory Modeling

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

Reference43 articles.

1. Household transmission of COVID-19 cases associated with SARS-CoV-2 Delta variant (B.1.617.2): national case-control study;Allen;Lancet Reg Health Eur,2021

2. Risk of hospital admission for patients with SARS-CoV-2 variant B.1.1.7: cohort analysis;Nyberg;BMJ,2021

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