A real-life setting evaluation of the effect of remdesivir on viral load in COVID-19 patients admitted to a large tertiary centre in Israel
- PMID: 33705849
- PMCID: PMC7939997
- DOI: 10.1016/j.cmi.2021.02.029
A real-life setting evaluation of the effect of remdesivir on viral load in COVID-19 patients admitted to a large tertiary centre in Israel
Abstract
Objectives: The effectiveness of remdesivir, a Food and Drug Administration-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 multicentre 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 patients admitted to a large tertiary centre 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 (cycle threshold 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 with 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.
Discussion: 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.
Keywords: Coronavirus disease 2019 (COVID-19); Hospitalization length; Remdesivir; SARS-CoV-2; Viral load.
Copyright © 2021 The Author(s). Published by Elsevier Ltd.. All rights reserved.
Figures


Similar articles
-
SARS-CoV-2 viral load is linked to remdesivir efficacy in severe Covid-19 admitted to intensive care.Sci Rep. 2024 Sep 6;14(1):20825. doi: 10.1038/s41598-024-71588-9. Sci Rep. 2024. PMID: 39242658 Free PMC article.
-
Case report study of the first five COVID-19 patients treated with remdesivir in France.Int J Infect Dis. 2020 Sep;98:290-293. doi: 10.1016/j.ijid.2020.06.093. Epub 2020 Jun 30. Int J Infect Dis. 2020. PMID: 32619764 Free PMC article.
-
Evaluation of the Effects of Remdesivir and Hydroxychloroquine on Viral Clearance in COVID-19 : A Randomized Trial.Ann Intern Med. 2021 Sep;174(9):1261-1269. doi: 10.7326/M21-0653. Epub 2021 Jul 13. Ann Intern Med. 2021. PMID: 34251903 Free PMC article. Clinical Trial.
-
Remdesivir: A Closer Look at Its Effect in COVID-19 Pandemic.Pharmacology. 2021;106(9-10):462-468. doi: 10.1159/000518440. Epub 2021 Aug 10. Pharmacology. 2021. PMID: 34515227 Free PMC article. Review.
-
Remdesivir in Coronavirus Disease 2019 (COVID-19) treatment: a review of evidence.Infection. 2021 Jun;49(3):401-410. doi: 10.1007/s15010-020-01557-7. Epub 2021 Jan 2. Infection. 2021. PMID: 33389708 Free PMC article. Review.
Cited by
-
Remdesivir reduced upper respiratory tract SARS-CoV-2 viral RNA concentration in COVID-19 patients who developed pneumonitis.J Infect. 2022 Dec;85(6):702-769. doi: 10.1016/j.jinf.2022.08.031. Epub 2022 Aug 31. J Infect. 2022. PMID: 36057383 Free PMC article. No abstract available.
-
SARS-CoV-2 viral load is linked to remdesivir efficacy in severe Covid-19 admitted to intensive care.Sci Rep. 2024 Sep 6;14(1):20825. doi: 10.1038/s41598-024-71588-9. Sci Rep. 2024. PMID: 39242658 Free PMC article.
-
Improving BNT162b2 mRNA Vaccine Tolerability without Efficacy Loss by Pidotimod Supplementation.Mediterr J Hematol Infect Dis. 2022 Mar 1;14(1):e2022023. doi: 10.4084/MJHID.2022.023. eCollection 2022. Mediterr J Hematol Infect Dis. 2022. PMID: 35444768 Free PMC article. No abstract available.
-
Early high antibody titre convalescent plasma for hospitalised COVID-19 patients: DAWn-plasma.Eur Respir J. 2022 Feb 10;59(2):2101724. doi: 10.1183/13993003.01724-2021. Print 2022 Feb. Eur Respir J. 2022. PMID: 34446469 Free PMC article. Clinical Trial.
-
Co-Administration of Remdesivir and Azithromycin May Protect against Intensive Care Unit Admission in COVID-19 Pneumonia Requiring Hospitalization: A Real-Life Observational Study.Antibiotics (Basel). 2022 Jul 14;11(7):941. doi: 10.3390/antibiotics11070941. Antibiotics (Basel). 2022. PMID: 35884195 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous