Remdesivir: Effectiveness and Safety in Hospitalized COVID-19 Patients—Analysis of Retrospectively Collected Data from Daily Practice in the Omicron Variant Era and Comparison with the Pre-Omicron Period

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has impacted global health. Remdesivir was approved based on clinical trials demonstrating improved outcomes in hospitalized patients. The ReEs-COVID19 study provides real-world evidence on its effectiveness and safety across two periods: Pre-Omicron and Omicron. This retrospective, observational cohort study included 1610 patients hospitalized with COVID-19, treated with remdesivir during Pre-Omicron (September 2020-February 2021; n = 606) and Omicron (June 2022-March 2023; n = 1004) periods. Primary endpoint: time to discharge; Hepatic/renal function abnormalities were also investigated. In the Omicron period patients were older and had more comorbidities but remdesivir was initiated earlier (median: 2 days from symptom onset) compared to the Pre-Omicron period (8 days). ICU admissions rates and direct COVID-19-related deaths were significantly lower, but overall 30-day mortality was higher during the Omicron period. Earlier remdesivir administration was associated with faster discharge. Abnormal liver tests and acute kidney injury were rare across both periods. ReEs-COVID19 confirmed remdesivir's effectiveness and safety in real-world clinical settings during both periods, underscoring its importance in treatment of hospitalized COVID-19 patients, especially when initiated earlier in the disease course. Further research is needed to evaluate its utility in specific subgroups (e.g., immuno-compromised) and in combination with other treatments.

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Publication Details

Journal
Microorganisms
Published
2025-09-25
DOI
https://doi.org/10.3390/microorganisms13102242
Citations
1
Primary Topic
COVID-19 Clinical Research Studies
Type
article
Field-Weighted Citation Impact
1.40

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article

Remdesivir: Effectiveness and Safety in Hospitalized COVID-19 Patients—Analysis of Retrospectively Collected Data from Daily Practice in the Omicron Variant Era and Comparison with the Pre-Omicron Period

Periklis Panagopoulos, Garyphallia Poulakou, Evmorfia Pechlivanidou, Sotirios P. Karagiannis et al.
1 citations
Microorganisms
COVID-19 Clinical Research Studies
1.40
article

Remdesivir: Effectiveness and Safety in Hospitalized COVID-19 Patients—Analysis of Retrospectively Collected Data from Daily Practice in the Omicron Variant Era and Comparison with the Pre-Omicron Period

Periklis Panagopoulos, Garyphallia Poulakou, Evmorfia Pechlivanidou, Sotirios P. Karagiannis, Nikos Pantazis, Vasileios Petrakis, Eirini Christaki, Eleni Polyzou, Ioannis Katsarolis, Theofani Rimpa, Vasiliki Georgakopoulou, Haralampos J Milionis, Nikolaos V. Sipsas, Anastasia Antoniadou, Giota Touloumi, Οlga Tsachouridou, Dimitra Kavatha, Karolina Akinosoglou, Diamantis P. Kofteridis, Vassiliki Rapti, Markos Marangos, Pinelopi Kazakou, Ioannis Kalomenidis, Symeon Metallidis
article en
1 citations

Abstract

Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has impacted global health. Remdesivir was approved based on clinical trials demonstrating improved outcomes in hospitalized patients. The ReEs-COVID19 study provides real-world evidence on its effectiveness and safety across two periods: Pre-Omicron and Omicron. This retrospective, observational cohort study included 1610 patients hospitalized with COVID-19, treated with remdesivir during Pre-Omicron (September 2020-February 2021; n = 606) and Omicron (June 2022-March 2023; n = 1004) periods. Primary endpoint: time to discharge; Hepatic/renal function abnormalities were also investigated. In the Omicron period patients were older and had more comorbidities but remdesivir was initiated earlier (median: 2 days from symptom onset) compared to the Pre-Omicron period (8 days). ICU admissions rates and direct COVID-19-related deaths were significantly lower, but overall 30-day mortality was higher during the Omicron period. Earlier remdesivir administration was associated with faster discharge. Abnormal liver tests and acute kidney injury were rare across both periods. ReEs-COVID19 confirmed remdesivir's effectiveness and safety in real-world clinical settings during both periods, underscoring its importance in treatment of hospitalized COVID-19 patients, especially when initiated earlier in the disease course. Further research is needed to evaluate its utility in specific subgroups (e.g., immuno-compromised) and in combination with other treatments.

MicroorganismsVol. 13(10)
University of Crete (GR), Democritus University of Thrace (GR), University of Patras (GR), University of Ioannina (GR), National and Kapodistrian University of Athens (GR), AHEPA University Hospital (GR), General University Hospital of Patras (GR), Laiko General Hospital of Athens (GR), University Hospital of Heraklion (GR), University Hospital of Ioannina (GR)
Gilead Sciences, European Centre for Disease Prevention and Control
Openalex Percentile: Top 16%
COVID-19 Clinical Research Studies
1.40
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