Ensitrelvir in hospitalized patients with COVID-19 who were moderately to severely immunocompromised: a single-center cohort study
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Published on: April 9, 2014
Masaya Yamato1, Masahiro Kinoshita2, Yuki Yoshida3
1Department of General Internal Medicine and Infectious Diseases, Rinku General Medical Center, Izumisano, Japan.
Insights
Ensitrelvir showed promising outcomes in hospitalized immunocompromised patients with COVID-19, demonstrating lower mortality compared to remdesivir in an exploratory study. Further research is needed due to the small sample size.
Area of Science:
- Infectious Diseases
- Virology
- Immunology
Background:
- Immunocompromised patients face a heightened risk of severe COVID-19.
- Effective antiviral treatments are crucial for this vulnerable population.
Purpose of the Study:
- To evaluate the clinical outcomes of ensitrelvir in hospitalized immunocompromised patients with COVID-19.
- To compare ensitrelvir's efficacy against remdesivir as a reference treatment.
Main Methods:
- A single-center retrospective cohort study was conducted.
- Patients with moderate/severe immunodeficiency receiving ensitrelvir or remdesivir were analyzed.
- Primary outcome was 28-day all-cause mortality; secondary outcomes included time to discharge and viral clearance.
Main Results:
- The study included 56 patients (22 ensitrelvir, 34 remdesivir).
- 28-day mortality was 4.5% for ensitrelvir and 8.8% for remdesivir.
- Inverse probability of treatment weighting (IPTW) suggested lower adjusted mortality for ensitrelvir (4.2% vs. 10.7%).
Conclusions:
- Ensitrelvir was associated with low mortality in this exploratory cohort.
- Comparisons with remdesivir require caution due to study limitations, including small sample size and potential treatment selection biases.
- Further investigation is warranted to confirm ensitrelvir's role in managing COVID-19 in immunocompromised individuals.
Background:
Immunocompromised patients have a risk of severe COVID-19.
Objectives:
To describe the outcomes of ensitrelvir in hospitalized immunocompromised patients with COVID-19, with remdesivir as a reference.
Design:
Single-center retrospective cohort study.
Methods:
We analyzed patients with moderate/severe immunodeficiency who received ensitrelvir or remdesivir as initial therapy. The primary outcome was 28-day all-cause mortality; secondary outcomes were time to discharge and viral clearance. Exploratory analyses used inverse probability of treatment weighting (IPTW) based on propensity scores and Cox proportional-hazards models.
Results:
Among 56 patients (22 ensitrelvir; 34 remdesivir), 28-day mortality was 4.5% versus 8.8%, respectively. Time to discharge and viral clearance were similar. IPTW-adjusted 28-day mortality was 4.2% with ensitrelvir and 10.7% with remdesivir (hazard ratio 0.39; 95% CI 0.04-3.64).
Conclusion:
In this small, single-center exploratory cohort, ensitrelvir was associated with low mortality, although comparison with remdesivir should be interpreted cautiously given treatment selection, treatment switching, and limited sample size.
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