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. 2022 Jan 21;71(3):96-102.
doi: 10.15585/mmwr.mm7103e1.

Racial and Ethnic Disparities in Receipt of Medications for Treatment of COVID-19 - United States, March 2020-August 2021

Racial and Ethnic Disparities in Receipt of Medications for Treatment of COVID-19 - United States, March 2020-August 2021

Jennifer L Wiltz et al. MMWR Morb Mortal Wkly Rep. .

Erratum in

  • Erratum: Vol. 71, No. 3.
    [No authors listed] [No authors listed] MMWR Morb Mortal Wkly Rep. 2022 Feb 25;71(8):325. doi: 10.15585/mmwr.mm7108a6. MMWR Morb Mortal Wkly Rep. 2022. PMID: 35202356 No abstract available.

Abstract

The COVID-19 pandemic has magnified longstanding health care and social inequities, resulting in disproportionately high COVID-19-associated illness and death among members of racial and ethnic minority groups (1). Equitable use of effective medications (2) could reduce disparities in these severe outcomes (3). Monoclonal antibody (mAb) therapies against SARS-CoV-2, the virus that causes COVID-19, initially received Emergency Use Authorization (EUA) from the Food and Drug Administration (FDA) in November 2020. mAbs are typically administered in an outpatient setting via intravenous infusion or subcutaneous injection and can prevent progression of COVID-19 if given after a positive SARS-CoV-2 test result or for postexposure prophylaxis in patients at high risk for severe illness. Dexamethasone, a commonly used steroid, and remdesivir, an antiviral drug that received EUA from FDA in May 2020, are used in inpatient settings and help prevent COVID-19 progression§ (2). No large-scale studies have yet examined the use of mAb by race and ethnicity. Using COVID-19 patient electronic health record data from 41 U.S. health care systems that participated in the PCORnet, the National Patient-Centered Clinical Research Network, this study assessed receipt of medications for COVID-19 treatment by race (White, Black, Asian, and Other races [including American Indian or Alaska Native, Native Hawaiian or Other Pacific Islander, and multiple or Other races]) and ethnicity (Hispanic or non-Hispanic). Relative disparities in mAb** treatment among all patients†† (805,276) with a positive SARS-CoV-2 test result and in dexamethasone and remdesivir treatment among inpatients§§ (120,204) with a positive SARS-CoV-2 test result were calculated. Among all patients with positive SARS-CoV-2 test results, the overall use of mAb was infrequent, with mean monthly use at 4% or less for all racial and ethnic groups. Hispanic patients received mAb 58% less often than did non-Hispanic patients, and Black, Asian, or Other race patients received mAb 22%, 48%, and 47% less often, respectively, than did White patients during November 2020-August 2021. Among inpatients, disparities were different and of lesser magnitude: Hispanic inpatients received dexamethasone 6% less often than did non-Hispanic inpatients, and Black inpatients received remdesivir 9% more often than did White inpatients. Vaccines and preventive measures are the best defense against infection; use of COVID-19 medications postexposure or postinfection can reduce morbidity and mortality and relieve strain on hospitals but are not a substitute for COVID-19 vaccination. Public health policies and programs centered around the specific needs of communities can promote health equity (4). Equitable receipt of outpatient treatments, such as mAb and antiviral medications, and implementation of prevention practices are essential to reducing existing racial and ethnic inequities in severe COVID-19-associated illness and death.

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Conflict of interest statement

All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. Amy K. Feehan receives research support from the Louisiana Public Health Institute. Joshua L. Denson reports grants from the American Diabetes Association, research funding from the Gordon and Betty Moore Foundation, the Society of Critical Care Medicine, and the National Institutes of Health (NIH); and personal fees from Astrazeneca, GlaxoSmithKline, and Guidepoint Global, outside the current work. Jason P. Block reports a grant from the National Institute of Diabetes and Digestive and Kidney Diseases, NIH and receipt of honoraria for participating in a panel discussion for the Kenner Foundation on “Early Detection of Pancreatic Cancer.” No other potential conflicts of interest were disclosed.

Figures

FIGURE
FIGURE
Monthly* percentage of COVID-19 patients (n = 805,276) receiving monoclonal antibody treatment, by race§ and ethnicity — 41 health care systems in the National Patient-Centered Clinical Research Network — United States, November 2020–August 2021 * Systematic temporal differences in medication receipt by race and ethnicity were assessed by pairwise Wilcoxon signed rank test. mAbs require administration by intravenous infusion or subcutaneous injection. § White race is the referent group; p-values for Black, Asian, and Other races are 0.004, 0.002, and 0.002, respectively. Non-Hispanic ethnicity is the referent group; p = 0.002 for Hispanic ethnicity.

References

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