Effect of Mass Artesunate-Amodiaquine Distribution on Mortality of Patients With Ebola Virus Disease During West African Outbreak

Author:

Garbern Stephanie C1ORCID,Yam Derrick2,Aluisio Adam R1,Cho Daniel K3,Kennedy Stephen B4,Massaquoi Moses4ORCID,Sahr Foday5,Perera Shiromi M6,Levine Adam C1,Liu Tao2

Affiliation:

1. Department of Emergency Medicine, Warren Alpert Medical School of Brown University, Providence, Rhode Island

2. Department of Biostatistics, Center for Statistical Sciences, Brown University School of Public Health, Providence, Rhode Island

3. Brown University, Providence, Rhode Island

4. Ministry of Health, Monrovia, Liberia

5. Sierra Leone Ministry of Defense, Freetown, Sierra Leone

6. International Medical Corps, Washington, DC

Abstract

AbstractBackgroundExperiments in vitro have shown that the drug amodiaquine may inhibit Ebola virus activity. During the Ebola virus disease (EVD) epidemic in West Africa in 2014–2016, 2 mass drug administrations (MDAs) of artesunate-amodiaquine (ASAQ) were implemented to decrease the burden of malaria. The objective of this study was to assess the effect of the ASAQ MDAs on the mortality of patients with EVD.MethodsA retrospective cohort design was used to analyze mortality data for patients with EVD admitted to 5 Ebola treatment units in Liberia and Sierra Leone. Patients admitted to the ETUs during the time period of ASAQ’s therapeutic effect from areas where the MDA was implemented were matched to controls not exposed to ASAQ, using a range of covariates, including malaria co-infection status, and a logistic regression analysis was performed. The primary outcome was Ebola treatment unit mortality.ResultsA total of 424 patients with EVD had sufficient data for analysis. Overall, the mortality of EVD patients was 57.5%. A total of 22 EVD patients were exposed to ASAQ during the MDAs and were found to have decreased risk of death compared with those not exposed in a matched analysis, but this did not reach statistical significance (relative risk, 0.63; 95% confidence interval, 0.37–1.07; P = .086).ConclusionsThere was a non–statistically significantly decreased risk of mortality in EVD patients exposed to ASAQ during the 2 MDAs as compared with EVD patients not exposed to ASAQ. Further prospective trials are needed to determine the direct effect of ASAQ on EVD mortality.

Funder

National Institute of Allergy and Infectious Diseases at the National Institutes of Health

National Institute of General Medical Sciences of the National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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