Hydroxychloroquine as Pre-exposure Prophylaxis for Coronavirus Disease 2019 (COVID-19) in Healthcare Workers: A Randomized Trial

Author:

Rajasingham Radha1ORCID,Bangdiwala Ananta S1,Nicol Melanie R1,Skipper Caleb P1,Pastick Katelyn A1ORCID,Axelrod Margaret L2,Pullen Matthew F1,Nascene Alanna A1,Williams Darlisha A1,Engen Nicole W1,Okafor Elizabeth C1,Rini Brian I2,Mayer Ingrid A2,McDonald Emily G3,Lee Todd C3,Li Peter4,MacKenzie Lauren J5,Balko Justin M2,Dunlop Stephen J16,Hullsiek Katherine H1,Boulware David R1,Lofgren Sarah M1,Abassi Mahsa,Balster Andrew,Collins Lindsey B,Drobot Glen,Krakower Douglas S,Lother Sylvain A,MacKay Dylan S,Meyer-Mueller Cameron,Selinsky Stephen,Solvason Dayna,Zarychanski Ryan,Zash Rebecca,

Affiliation:

1. University of Minnesota, Minneapolis, Minnesota, USA

2. Vanderbilt University Medical Center, Nashville, Tennessee, USA

3. Research Institute of the McGill University Health Centre and the Clinical Practice Assessment Unit, Department of Medicine, McGill University, Montreal, Quebec, Canada

4. Oregon Health and Science University, Portland, Oregon, USA

5. Section of Infectious Diseases, Department of Internal Medicine, University of Manitoba, Winnipeg, Manitoba, Canada

6. Hennepin Healthcare, Minneapolis, Minnesota, USA

Abstract

Abstract Background Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a rapidly emerging virus causing the ongoing coronavirus disease 2019 (COVID-19) pandemic with no known effective prophylaxis. We investigated whether hydroxychloroquine could prevent SARS-CoV-2 in healthcare workers at high risk of exposure. Methods We conducted a randomized, double-blind, placebo-controlled clinical trial of healthcare workers with ongoing exposure to persons with SARS-CoV-2, including those working in emergency departments, intensive care units, COVID-19 hospital wards, and first responders. Participants across the United States and in the Canadian province of Manitoba were randomized to hydroxychloroquine loading dose then 400 mg once or twice weekly for 12 weeks. The primary endpoint was confirmed or probable COVID-19–compatible illness. We measured hydroxychloroquine whole-blood concentrations. Results We enrolled 1483 healthcare workers, of whom 79% reported performing aerosol-generating procedures. The incidence of COVID-19 (laboratory-confirmed or symptomatic compatible illness) was 0.27 events/person-year with once-weekly and 0.28 events/person-year with twice-weekly hydroxychloroquine compared with 0.38 events/person-year with placebo. For once-weekly hydroxychloroquine prophylaxis, the hazard ratio was .72 (95% CI, .44–1.16; P = .18) and for twice-weekly was .74 (95% CI, .46–1.19; P = .22) compared with placebo. Median hydroxychloroquine concentrations in whole blood were 98 ng/mL (IQR, 82–120) with once-weekly and 200 ng/mL (IQR, 159–258) with twice-weekly dosing. Hydroxychloroquine concentrations did not differ between participants who developed COVID-19–compatible illness (154 ng/mL) versus participants without COVID-19 (133 ng/mL; P = .08). Conclusions Pre-exposure prophylaxis with hydroxychloroquine once or twice weekly did not significantly reduce laboratory-confirmed COVID-19 or COVID-19–compatible illness among healthcare workers. Clinical Trials Registration Clinicaltrials.gov NCT04328467.

Funder

National Institute of Allergy and Infectious Diseases

National Institute of Mental Health

Fogarty International Center

National Institute of Neurological Disorders and Stroke

Doris Duke Charitable Foundation

National Institutes of Health

Fonds de Recherche du Québec - Santé

Manitoba Medical Service Foundation

Research Manitoba

National Center for Advancing Translational Sciences

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

Reference25 articles.

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