Characteristics and Factors Associated with COVID-19 Infection, Hospitalization, and Mortality Across Race and Ethnicity.

COVID-19 SARS-CoV-2 health disparity public health race/ethnicity

Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
12 Feb 2021
Historique:
pubmed: 18 2 2021
medline: 18 2 2021
entrez: 17 2 2021
Statut: epublish

Résumé

Data on the characteristics of COVID-19 patients disaggregated by race/ethnicity remain limited. We evaluated the sociodemographic and clinical characteristics of patients across racial/ethnic groups and assessed their associations with COVID-19 outcomes. This retrospective cohort study examined 629,953 patients tested for SARS-CoV-2 in a large health system spanning California, Oregon, and Washington between March 1 and December 31, 2020. Sociodemographic and clinical characteristics were obtained from electronic health records. Odds of SARS-CoV-2 infection, COVID-19 hospitalization, and in-hospital death were assessed with multivariate logistic regression. 570,298 patients with known race/ethnicity were tested for SARS-CoV-2, of whom 27.8% were non-White minorities. 54,645 individuals tested positive, with minorities representing 50.1%. Hispanics represented 34.3% of infections but only 13.4% of tests. While generally younger than White patients, Hispanics had higher rates of diabetes but fewer other comorbidities. 8,536 patients were hospitalized and 1,246 died, of whom 56.1% and 54.4% were non-White, respectively. Racial/ethnic distributions of outcomes across the health system tracked with state-level statistics. Increased odds of testing positive and hospitalization were associated with all minority races/ethnicities. Hispanic patients also exhibited increased morbidity, and Hispanic race/ethnicity was associated with in-hospital mortality (OR: 1.39 [95% CI: 1.14-1.70]). Major healthcare disparities were evident, especially among Hispanics who tested positive at a higher rate, required excess hospitalization and mechanical ventilation, and had higher odds of in-hospital mortality despite younger age. Targeted, culturally-responsive interventions and equitable vaccine development and distribution are needed to address the increased risk of poorer COVID-19 outcomes among minority populations.

Sections du résumé

Background UNASSIGNED
Data on the characteristics of COVID-19 patients disaggregated by race/ethnicity remain limited. We evaluated the sociodemographic and clinical characteristics of patients across racial/ethnic groups and assessed their associations with COVID-19 outcomes.
Methods UNASSIGNED
This retrospective cohort study examined 629,953 patients tested for SARS-CoV-2 in a large health system spanning California, Oregon, and Washington between March 1 and December 31, 2020. Sociodemographic and clinical characteristics were obtained from electronic health records. Odds of SARS-CoV-2 infection, COVID-19 hospitalization, and in-hospital death were assessed with multivariate logistic regression.
Results UNASSIGNED
570,298 patients with known race/ethnicity were tested for SARS-CoV-2, of whom 27.8% were non-White minorities. 54,645 individuals tested positive, with minorities representing 50.1%. Hispanics represented 34.3% of infections but only 13.4% of tests. While generally younger than White patients, Hispanics had higher rates of diabetes but fewer other comorbidities. 8,536 patients were hospitalized and 1,246 died, of whom 56.1% and 54.4% were non-White, respectively. Racial/ethnic distributions of outcomes across the health system tracked with state-level statistics. Increased odds of testing positive and hospitalization were associated with all minority races/ethnicities. Hispanic patients also exhibited increased morbidity, and Hispanic race/ethnicity was associated with in-hospital mortality (OR: 1.39 [95% CI: 1.14-1.70]).
Conclusion UNASSIGNED
Major healthcare disparities were evident, especially among Hispanics who tested positive at a higher rate, required excess hospitalization and mechanical ventilation, and had higher odds of in-hospital mortality despite younger age. Targeted, culturally-responsive interventions and equitable vaccine development and distribution are needed to address the increased risk of poorer COVID-19 outcomes among minority populations.

Identifiants

pubmed: 33594379
doi: 10.1101/2020.10.14.20212803
pmc: PMC7885938
pii:
doi:

Types de publication

Preprint

Langues

eng

Commentaires et corrections

Type : UpdateIn

Déclaration de conflit d'intérêts

Conflicts of Interest JRH reports fees and support from PACT Pharma, Isoplexis, Indi Molecular, Nanostring, Merck, Atlasxomics outside the submitted work. JDG performed contracted research with Gilead Sciences, Regeneron Pharmaceuticals and Eli Lilly; JDG also has received grants from Monogram Biosciences and Viracor outside of the submitted work. Dr. Diaz reports other work from Gilead Sciences, Lexicon Pharmaceuticals, Safeology, Inc, Regeneron, Roche, Boehringer Ingelheim, and Edesa Biotech outside the submitted work.

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Auteurs

Chengzhen L Dai (CL)

Institute for Systems Biology, Seattle, WA, USA.

Sergey A Kornilov (SA)

Institute for Systems Biology, Seattle, WA, USA.

Ryan T Roper (RT)

Institute for Systems Biology, Seattle, WA, USA.

Hannah Cohen-Cline (H)

Providence Center for Outcomes Research and Education, Providence Health System, Renton, WA, USA.

Kathleen Jade (K)

Institute for Systems Biology, Seattle, WA, USA.

Brett Smith (B)

Institute for Systems Biology, Seattle, WA, USA.

James R Heath (JR)

Institute for Systems Biology, Seattle, WA, USA.
Department of Bioengineering, University of Washington, Seattle, WA, USA.

George Diaz (G)

Providence Regional Medical Center, Everett, WA, USA.

Jason D Goldman (JD)

Swedish Center for Research and Innovation, Swedish Medical Center, Seattle, WA, USA.
Division of Allergy & Infectious Diseases, University of Washington, Seattle, WA, USA.

Andrew T Magis (AT)

Institute for Systems Biology, Seattle, WA, USA.

Jennifer J Hadlock (JJ)

Institute for Systems Biology, Seattle, WA, USA.

Classifications MeSH