Remdesivir for Patients Hospitalized with COVID-19 Severe Pneumonia: A National Cohort Study (Remdeco-19)
- PMID: 36362773
- PMCID: PMC9654065
- DOI: 10.3390/jcm11216545
Remdesivir for Patients Hospitalized with COVID-19 Severe Pneumonia: A National Cohort Study (Remdeco-19)
Abstract
Background: Given the rapidly evolving pandemic of COVID-19 in 2020, authorities focused on the repurposing of available drugs to develop timely and cost-effective therapeutic strategies. Evidence suggested the potential utility of remdesivir in the framework of an early access program. REMDECO-19 is a multicenter national cohort study assessing the ability of remdesivir to improve the outcome of patients hospitalized with COVID-19.
Methods: We conducted a retrospective real-life study that included all patients from the early access program of remdesivir in France. The primary endpoint was the clinical course evolution of critically ill and hospitalized COVID-19 patients treated with remdesivir. Secondary endpoints were the SOFA score evolution within 29 days following the admission and mortality at 29 and 90 days.
Results: Eighty-five patients were enrolled in 22 sites from January to April 2020. The median WHO and SOFA scores were respectively reduced by two and six points between days 1 and 29. Improvement in the WHO-CPS and the SOFA score were observed in 83.5% and 79.3% of patients, respectively, from day 10. However, there was no effect of remdesivir on the 90-day survival based on the control cohort for hospitalized COVID-19 patients with invasive ventilation.
Conclusions: SOFA score appeared to be an attractive approach to assess remdesivir efficacy and stratify its utilization or not in critically ill patients with COVID-19. This study brings a new clinical benchmark for therapeutic decision making and supports the use of remdesivir for some hospitalized COVID-19 patients.
Keywords: COVID-19; SARS-CoV-2; pneumonia; remdesivir; survival.
Conflict of interest statement
F.B. reports consulting and lecture fees from MSD and lecture fees from Biomérieux, outside the scope of the submitted work. J.Z. reports consulting fees from AstraZeneca, outside the scope of the submitted work. J.G. reports grants from Gilead and ViiVHealthcare and personal fees from MSD, Gilead, Astra Zeneca, Roche, and ViiVHealthcare, outside the scope of the submitted work. F.P. reports consulting fees and grants from Alexion Pharma and consulting and personal fees from Gilead outside the scope of the submitted work.
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