Real-life experience with remdesivir for treatment of hospitalized coronavirus disease 2019 patients: matched case-control study from a large tertiary hospital registry
Aim To evaluate the association of remdesivir use and the
survival of hospitalized patients with coronavirus disease
2019 (COVID-19).
Methods We retrospectively reviewed the medical re
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cords of 5959 COVID-19 patients admitted to our tertiarylevel hospital from March 2020 to June 2021. A total of 876
remdesivir-treated patients were matched with 876 con
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trol patients in terms of age, sex, Charlson comorbidity in
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dex (CCI), WHO-defined COVID-19 severity on admission,
and oxygen requirement at the time of remdesivir use.
Results Among 1752 COVID-19 patients (median age 66
years, 61.8% men), 1405 (80.2%) had severe and 311 (17.8%)
had critically severe COVID-19 on admission. Remdesivir
was given at a median of one day after hospital admission
and at a median of eight days from the onset of symptoms.
Overall, 645 (73.6%) patients received remdesivir before
high-flow oxygen therapy (HFOT) or mechanical ventila
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tion (MV), 198 (22.6%) after HFOT institution, and 83 (9.5%)
after MV institution. Remdesivir use was associated with
improved survival in the entire cohort (hazard ratio 0.79, P=0.006). Survival benefit was evident among patients receiving remdesivir during low-flow oxygen requirement
(hazard ratio 0.61,