Risk of hospitalization and sequelae in patients with COVID‐19 treated with 3‐day early remdesivir vs. controls in the vaccine and Omicron era: A real‐life cohort study
Recently, a benefit from administration of a 3‐day course of early remdesivir (ER) in the outpatients' setting was reported. However, real‐life data on its use is scarce. Therefore, we explored the ER clinical outcome in our outpatients' s cohort, compared to untreated controls. We include...
Gespeichert in:
Veröffentlicht in: | Journal of medical virology 2023-03, Vol.95 (3), p.e28660-n/a |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Recently, a benefit from administration of a 3‐day course of early remdesivir (ER) in the outpatients' setting was reported. However, real‐life data on its use is scarce. Therefore, we explored the ER clinical outcome in our outpatients' s cohort, compared to untreated controls. We included all patients who were prescribed ER from February to May 2022 and followed them up for 3 months and compared patients who received treatment with untreated controls. In the two groups the following outcomes were investigated: hospitalization and mortality rate, time of negativization and symptom's resolution, and postacute coronavirus disease 19 (COVID‐19) syndrome prevalence. Overall, 681 patients were analyzed, mostly females (53.6%), and with a median age of 66 years (interquartile range: 54–77), 316 (46.4%) patients received ER, and 365 (53.6%) did not receive antiviral treatment (control group). Overall, 8.5% patients eventually required oxygen support, 8.7% were hospitalized for COVID‐19, and 1.5% died. Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) immunization and ER (adjusted odds ratio [aOR]: 0.049 [0.015; 0.16], p |
---|---|
ISSN: | 0146-6615 1096-9071 |
DOI: | 10.1002/jmv.28660 |