Remdesivir for the treatment of patients hospitalized with COVID-19 receiving supplemental oxygen: a targeted literature review and meta-analysis

Rachel Beckerman*, Andrea Gori, Sushanth Jeyakumar, Jakob J. Malin, Roger Paredes, Pedro Póvoa, Nathaniel J. Smith, Armando Teixeira-Pinto

*Kontaktforfatter

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

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Abstract

This network meta-analysis (NMA) assessed the efficacy of remdesivir in hospitalized patients with COVID-19 requiring supplemental oxygen. Randomized controlled trials of hospitalized patients with COVID-19, where patients were receiving supplemental oxygen at baseline and at least one arm received treatment with remdesivir, were identified. Outcomes included mortality, recovery, and no longer requiring supplemental oxygen. NMAs were performed for low-flow oxygen (LFO2); high-flow oxygen (HFO2), including NIV (non-invasive ventilation); or oxygen at any flow (AnyO2) at early (day 14/15) and late (day 28/29) time points. Six studies were included (N = 5245 patients) in the NMA. Remdesivir lowered early and late mortality among AnyO2 patients (risk ratio (RR) 0.52, 95% credible interval (CrI) 0.34–0.79; RR 0.81, 95%CrI 0.69–0.95) and LFO2 patients (RR 0.21, 95%CrI 0.09–0.46; RR 0.24, 95%CrI 0.11–0.48); no improvement was observed among HFO2 patients. Improved early and late recovery was observed among LFO2 patients (RR 1.22, 95%CrI 1.09–1.38; RR 1.17, 95%CrI 1.09–1.28). Remdesivir also lowered the requirement for oxygen support among all patient subgroups. Among hospitalized patients with COVID-19 requiring supplemental oxygen at baseline, use of remdesivir compared to best supportive care is likely to improve the risk of mortality, recovery and need for oxygen support in AnyO2 and LFO2 patients.

OriginalsprogEngelsk
Artikelnummer9622
TidsskriftScientific Reports
Vol/bind12
Antal sider11
ISSN2045-2322
DOI
StatusUdgivet - 10. jun. 2022

Bibliografisk note

Funding Information:
AG has received research grants, advisory board fees, and travel grants from Angelini, Menarini, Gilead Sciences, Janssen, MSD, Novarti, Pfizer, ViiV, and GSK. JJM received consulting fees from Maple Health Group and Atriva Therapeutics GmbH, reimbursements for travel expenses from Gilead Sciences, ViiV Healthcare and Correvio Pharma, institutional research funding from the National Institutes of Health. PP has research grants, advisory boards fees from Technophage, MSD, Abionic and Gilead Sciences. RP has received research support (awarded to his institution) and participated in advisory boards from Gilead, ViiV Healthcare, MSD, Lilly and Theratechnologies. RB, SJ, RP, MJS and ATP have no competing interests to declare.

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