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Clinical Characteristics and Predictors of Outcomes of Hospitalized Patients With Coronavirus Disease 2019 in a Multiethnic London National Health Service Trust: A Retrospective Cohort Study.

Perez-Guzman, PN; Daunt, A; Mukherjee, S; Crook, P; Forlano, R; Kont, MD; Løchen, A; Vollmer, M; Middleton, P; Judge, R; et al. Perez-Guzman, PN; Daunt, A; Mukherjee, S; Crook, P; Forlano, R; Kont, MD; Løchen, A; Vollmer, M; Middleton, P; Judge, R; Harlow, C; Soubieres, A; Cooke, G; White, PJ; Hallett, TB; Aylin, P; Ferguson, N; Hauck, K; Thursz, MR; Nayagam, S (2021) Clinical Characteristics and Predictors of Outcomes of Hospitalized Patients With Coronavirus Disease 2019 in a Multiethnic London National Health Service Trust: A Retrospective Cohort Study. Clin Infect Dis, 73 (11). e4047-e4057. ISSN 1537-6591 https://doi.org/10.1093/cid/ciaa1091
SGUL Authors: Crook, Peter Andrew

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Abstract

BACKGROUND: Emerging evidence suggests ethnic minorities are disproportionately affected by coronavirus disease 2019 (COVID-19). Detailed clinical analyses of multicultural hospitalized patient cohorts remain largely undescribed. METHODS: We performed regression, survival, and cumulative competing risk analyses to evaluate factors associated with mortality in patients admitted for COVID-19 in 3 large London hospitals between 25 February and 5 April, censored as of 1 May 2020. RESULTS: Of 614 patients (median age, 69 [interquartile range, 25] years) and 62% male), 381 (62%) were discharged alive, 178 (29%) died, and 55 (9%) remained hospitalized at censoring. Severe hypoxemia (adjusted odds ratio [aOR], 4.25 [95% confidence interval {CI}, 2.36-7.64]), leukocytosis (aOR, 2.35 [95% CI, 1.35-4.11]), thrombocytopenia (aOR [1.01, 95% CI, 1.00-1.01], increase per 109 decrease), severe renal impairment (aOR, 5.14 [95% CI, 2.65-9.97]), and low albumin (aOR, 1.06 [95% CI, 1.02-1.09], increase per gram decrease) were associated with death. Forty percent (n = 244) were from black, Asian, and other minority ethnic (BAME) groups, 38% (n = 235) were white, and ethnicity was unknown for 22% (n = 135). BAME patients were younger and had fewer comorbidities. Although the unadjusted odds of death did not differ by ethnicity, when adjusting for age, sex, and comorbidities, black patients were at higher odds of death compared to whites (aOR, 1.69 [95% CI, 1.00-2.86]). This association was stronger when further adjusting for admission severity (aOR, 1.85 [95% CI, 1.06-3.24]). CONCLUSIONS: BAME patients were overrepresented in our cohort; when accounting for demographic and clinical profile of admission, black patients were at increased odds of death. Further research is needed into biologic drivers of differences in COVID-19 outcomes by ethnicity.

Item Type: Article
Additional Information: © The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: COVID-19, ethnic minority groups, mortality, Aged, COVID-19, Cohort Studies, Ethnic and Racial Minorities, Female, Humans, London, Male, Retrospective Studies, SARS-CoV-2, State Medicine, Humans, Retrospective Studies, Cohort Studies, Aged, State Medicine, London, Female, Male, COVID-19, SARS-CoV-2, Ethnic and Racial Minorities, COVID-19, ethnic minority groups, mortality, Aged, COVID-19, Cohort Studies, Ethnic and Racial Minorities, Female, Humans, London, Male, Retrospective Studies, SARS-CoV-2, State Medicine, Microbiology, 06 Biological Sciences, 11 Medical and Health Sciences
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: Clin Infect Dis
ISSN: 1537-6591
Language: eng
Dates:
DateEvent
6 December 2021Published
7 August 2020Published Online
27 July 2020Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
MC_PC_19012Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/R015600/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
RP-2016-07-012Department of Healthhttp://dx.doi.org/10.13039/501100000276
UNSPECIFIEDDepartment for International Developmenthttp://dx.doi.org/10.13039/501100000278
PubMed ID: 32766823
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/114301
Publisher's version: https://doi.org/10.1093/cid/ciaa1091

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