Retrospective Analysis of the Effectiveness of Remdesivir in COVID-19 Treatment during Periods Dominated by Delta and Omicron SARS-CoV-2 Variants in Clinical Settings.
Krystyna DobrowolskaDorota Zarębska-MichalukMichał BrzdękPiotr RzymskiMagdalena RogalskaAnna M Moniuszko-MalinowskaDorota KozielewiczMarcin HawroMarta RoratKatarzyna SikorskaJerzy JaroszewiczJustyna Dominika KowalskaRobert FlisiakPublished in: Journal of clinical medicine (2023)
Continuous evaluation of real-world treatment effectiveness of COVID-19 medicines is required due to the ongoing evolution of SARS-CoV-2 and the possible emergence of resistance. Therefore, this study aimed to analyze, in a retrospective manner, the outcomes in patients hospitalized with COVID-19 during the pandemic waves dominated by Delta and Omicron variants and treated with remdesivir (RDV) ( n = 762) in comparison to a demographically and clinically matched group not treated with any antivirals ( n = 1060). A logistic regression analysis revealed that RDV treatment was associated with a significantly lower risk of death during both Delta wave (OR = 0.42, 95%CI: 0.29-0.60; p < 0.0001) and Omicron-dominated period (OR = 0.56, 95%CI: 0.35-0.92; p = 0.02). Moreover, RDV-treated groups were characterized by a lower percentage of patients requiring mechanical ventilation, but the difference was not statistically significant. This study is the first real-world evidence that RDV remains effective during the dominance of more pathogenic SARS-CoV-2 variants and those that cause a milder course of the disease, and continues to be an essential element of COVID-19 therapy.
Keyphrases
- sars cov
- coronavirus disease
- respiratory syndrome coronavirus
- newly diagnosed
- end stage renal disease
- mechanical ventilation
- ejection fraction
- chronic kidney disease
- copy number
- systematic review
- prognostic factors
- peritoneal dialysis
- randomized controlled trial
- gene expression
- patient reported outcomes
- intensive care unit
- dna methylation
- metabolic syndrome
- acute respiratory distress syndrome
- insulin resistance
- single cell
- skeletal muscle
- patient reported
- bone marrow