E. Goldberg, H. Ben Zvi, Liron Sheena, Summer Sofer, I. Krause, E. Sklan, A. Shlomai
Clinical Microbiology and Infection, 2021
Objectives The effectiveness of remdesivir, a Food and Drug Administration (FDA) approved drug for severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), has been repeatedly questioned during the current coronavirus disease 2019 (COVID-19) pandemic. Most of the recently reported studies were randomized controlled multicenter clinical trials. Our goal was to test the efficiency of remdesivir in reducing nasopharyngeal viral load and hospitalization length in a real-life setting in admitted patients in a large tertiary center in Israel. Methods A total of 142 COVID-19 patients found to have at least three reported SARS-CoV-2 quantitative RT-PCR tests during hospitalization were selected for this study. Of these, 29 patients received remdesivir, while the remaining non-treated 113 patients served as controls. Results Among the tested parameters, the control and remdesivir groups differed significantly only in the intubation rates. Remdesivir treatment did not significantly affect nasopharyngeal viral load, as determined by comparing the differences between the first and last cycle threshold values of the SARS-CoV-2 quantitative RT-PCR tests performed during hospitalization (Ct 7.07±6.85 vs. 7.08±7.27, p=0.977 in the control and treated groups, respectively). Remdesivir treatment shortened hospitalization length by less than a day compared to non-treated controls and by 3.1 days when non-intubated patients from both groups were compared. These differences, however, were not statistically significant, possibly because of the small size of the remdesivir group. Conclusions Remdesivir was not associated with nasopharyngeal viral load changes, but our study had a significant disease severity baseline imbalance and was not powered to detect viral load or clinical differences.
Cited by 7 publications.
Field of study: Medicine