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Impact of Severe Acute Respiratory Syndrome Coronavirus 2 Variants on Inpatient Clinical Outcome.
Robinson, Matthew L; Morris, C Paul; Betz, Joshua F; Zhang, Yifan; Bollinger, Robert; Wang, Natalie; Thiemann, David R; Fall, Amary; Eldesouki, Raghda E; Norton, Julie M; Gaston, David C; Forman, Michael; Luo, Chun Huai; Zeger, Scott L; Gupta, Amita; Garibaldi, Brian T; Mostafa, Heba H.
  • Robinson ML; Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Morris CP; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Betz JF; National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Zhang Y; Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Bollinger R; Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Wang N; Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Thiemann DR; Krieger School of Arts & Sciences, Johns Hopkins University, Baltimore, Maryland, USA.
  • Fall A; Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Eldesouki RE; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Norton JM; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Gaston DC; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Forman M; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Luo CH; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Zeger SL; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Gupta A; Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Garibaldi BT; Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Mostafa HH; Division of Pulmonary and Critical Care, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Clin Infect Dis ; 76(9): 1539-1549, 2023 05 03.
Article in English | MEDLINE | ID: covidwho-20242038
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Inpatients Type of study: Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Clin Infect Dis Journal subject: Communicable Diseases Year: 2023 Document Type: Article Affiliation country: Cid

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Inpatients Type of study: Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Clin Infect Dis Journal subject: Communicable Diseases Year: 2023 Document Type: Article Affiliation country: Cid