Remdesivir’s effectiveness in treating severe COVID-19—a retrospective cohort from Pakistan

The efficacy of remdesivir in the treatment of severe COVID-19 is contentious, characterized by inconsistent findings regarding mortality benefit and recovery time across clinical trials such as ACTT-1 and WHO Solidarity. The ACTT-1 trial indicated a decrease in recovery time, however the WHO Solidarity trial revealed no substantial mortality advantage. Due to these inconsistencies, additional real-world data are required, especially in resource-constrained environments where treatment regimens may vary. This study assesses the efficacy of remdesivir in conjunction with standard care (R-SOC) versus standard care alone (SOC) in patients presenting with severe COVID-19 pneumonia in Pakistan. From June 2021 to December 2022, all consecutive patients diagnosed with severe COVID-19 pneumonia who were admitted to Dr. Ziauddin Hospital North Nazimabad in Karachi, Pakistan, were included in a retrospective, comparative cohort study. In order to evaluate treatment outcomes, these patients were enrolled in a retrospective, comparative cohort research that included survival analysis. The SOC group had a considerably greater discharge rate compared to the R-SOC group (70.3% vs. 57.4%; p < 0.001). The fatality rate was notably higher in the R-SOC group than in the SOC group (35% vs. 19%; p = 0.001). Furthermore, compared to the SOC group, a greater percentage of patients in the R-SOC group needed invasive mechanical ventilation or admission to the intensive care unit (ICU) (24.8% vs. 10.5%; p = 0.001, and 13% vs. 5.6%; p = 0.001, respectively). Patients receiving SOC were also discharged sooner than those receiving R-SOC (6.23 vs. 8.38 days; Log Rank p = 0.001). Accordingly, patients in the R-SOC group had a substantially increased risk of mortality (HR 2.082, 95% CI 1.603–2.704, p = 0.001), ICU admission (HR 1.603, 95% CI 1.143–2.248, p = 0.006), and invasive mechanical ventilation (HR 2.717, 95% CI 1.661–4.442, p = 0.001). Remdesivir use was associated with the higher rates of intensive care unit admission, a longer hospital stay, a higher requirement for invasive mechanical ventilation, and an increased risk of death.

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Journal
Discover Medicine
Published
2025-10-17
DOI
https://doi.org/10.1007/s44337-025-00517-0
Primary Topic
COVID-19 Clinical Research Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

Remdesivir’s effectiveness in treating severe COVID-19—a retrospective cohort from Pakistan

Fnu Sameeullah, Yameena Noman Khan, Syed Ali Raza, Muhammad Saad Jafri et al.
Discover Medicine
COVID-19 Clinical Research Studies
article

Remdesivir’s effectiveness in treating severe COVID-19—a retrospective cohort from Pakistan

Fnu Sameeullah, Yameena Noman Khan, Syed Ali Raza, Muhammad Saad Jafri, Jamil Muqtadir, Irshad Batool, Muhammad Umair Khan, S. Ehsan
article en

Abstract

The efficacy of remdesivir in the treatment of severe COVID-19 is contentious, characterized by inconsistent findings regarding mortality benefit and recovery time across clinical trials such as ACTT-1 and WHO Solidarity. The ACTT-1 trial indicated a decrease in recovery time, however the WHO Solidarity trial revealed no substantial mortality advantage. Due to these inconsistencies, additional real-world data are required, especially in resource-constrained environments where treatment regimens may vary. This study assesses the efficacy of remdesivir in conjunction with standard care (R-SOC) versus standard care alone (SOC) in patients presenting with severe COVID-19 pneumonia in Pakistan. From June 2021 to December 2022, all consecutive patients diagnosed with severe COVID-19 pneumonia who were admitted to Dr. Ziauddin Hospital North Nazimabad in Karachi, Pakistan, were included in a retrospective, comparative cohort study. In order to evaluate treatment outcomes, these patients were enrolled in a retrospective, comparative cohort research that included survival analysis. The SOC group had a considerably greater discharge rate compared to the R-SOC group (70.3% vs. 57.4%; p < 0.001). The fatality rate was notably higher in the R-SOC group than in the SOC group (35% vs. 19%; p = 0.001). Furthermore, compared to the SOC group, a greater percentage of patients in the R-SOC group needed invasive mechanical ventilation or admission to the intensive care unit (ICU) (24.8% vs. 10.5%; p = 0.001, and 13% vs. 5.6%; p = 0.001, respectively). Patients receiving SOC were also discharged sooner than those receiving R-SOC (6.23 vs. 8.38 days; Log Rank p = 0.001). Accordingly, patients in the R-SOC group had a substantially increased risk of mortality (HR 2.082, 95% CI 1.603–2.704, p = 0.001), ICU admission (HR 1.603, 95% CI 1.143–2.248, p = 0.006), and invasive mechanical ventilation (HR 2.717, 95% CI 1.661–4.442, p = 0.001). Remdesivir use was associated with the higher rates of intensive care unit admission, a longer hospital stay, a higher requirement for invasive mechanical ventilation, and an increased risk of death.

Discover MedicineVol. 2(1)
Boston Medical Center (US), Shaheed Mohtarma Benazir Bhutto Medical University (PK), Ziauddin Hospital (PK), Ziauddin University (PK)
Openalex Percentile: Top 65%
COVID-19 Clinical Research Studies
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