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Year : 2021  |  Volume : 21  |  Issue : 2  |  Page : 43-50

Randomized controlled trials of remdesivir in hospitalized coronavirus disease 2019 patients: A meta-analysis

1 Department of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan; Division of Research and Academic Affairs, Larkin Health System, South Miami, Florida, USA
2 Division of Research and Academic Affairs, Larkin Health System, South Miami, Florida, USA; Department of Research and Publication, Fatima Jinnah Medical University, Lahore, Pakistan
3 Division of Research and Academic Affairs, Larkin Health System, South Miami, Florida, USA

Correspondence Address:
Dr. Azza Sarfraz
Department of Pediatrics and Child Health, Faculty Office Building, Aga Khan University, P.O Box 3500, Stadium Road, Karachi 74800

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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/2452-2473.309139

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BACKGROUND: The first cases of the coronavirus disease 2019 (COVID-19) were reported in Wuhan, China. No antiviral treatment options are currently available with proven clinical efficacy. However, preliminary findings from phase III trials suggest that remdesivir is an effective and safe treatment option for COVID-19 patients with both moderate and severe disease. OBJECTIVE: The aim of the present meta-analysis was to investigate whether remdesivir was effective for treating COVID-19 including reduced in-hospital adverse events, oxygen support, and mortality rates. METHODS: According to the PRISMA reporting guidelines, a review was conducted from January 1, 2020, until August 25, 2020, with MeSH terms including COVID-19, COVID, coronavirus, SARS-CoV-2, remdesivir, adenosine nucleoside triphosphate analog, and Veklury using MEDLINE, Scopus, and CINAHL Plus. A modified Delphi process was utilized to include the studies and ensure that the objectives were addressed. Using dichotomous data for select values, the unadjusted odds ratios (ORs) were calculated applying Mantel–Haenszel random-effects method in Review Manager 5.4. RESULTS: Randomized controlled trials pooled in 3013 participants with 46.3% (n = 1395) in the remdesivir group and 53.7% (n = 1618) in the placebo group. The placebo group had a higher risk of mortality as compared to the intervention group with significant OR (0.61) (95% confidence interval of 0.45–0.82; P = 0.001). There was minimal heterogeneity among the studies (I2 = 0%). CONCLUSIONS: Our findings suggest that remdesivir extends clinical benefits by reducing mortality, adverse events, and oxygen support in moderate to severely ill COVID-19 patients. Concerted efforts and further randomized placebo-controlled trials are warranted to examine the potency of antiviral drugs and immunopathological host responses contributing to the severity of COVID-19.

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