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Efficacy and optimal timing of sivelestat in critically ill patients with COVID-19: a multicenter retrospective
Qi Zhang1,2, Yijie Liu2, Bowen Ran2,3,4
1Beijing University of Chinese Medicine, Beijing, 100105, China.
Insights
Sivelestat may improve survival in severe COVID-19 patients. This retrospective study found sivelestat associated with reduced 28-day mortality in intensive care unit patients, suggesting a potential therapeutic benefit.
Area of Science:
- Critical Care Medicine
- Pharmacology
- Infectious Diseases
Background:
- Cytokine storm is key in severe COVID-19 progression.
- Sivelestat exhibits anti-inflammatory properties.
- Sivelestat is a potential therapeutic for severe COVID-19.
Purpose of the Study:
- To evaluate sivelestat's efficacy in severe COVID-19 patients.
- To assess the impact of sivelestat on mortality and secondary outcomes.
Main Methods:
- Multicenter retrospective study in China.
- Involved intensive care unit patients with severe COVID-19.
- 1:2 propensity score matching (PSM) used for analysis.
Main Results:
- Sivelestat associated with improved 28-day survival (53.55% vs. 40.87%, P=0.03).
- No significant differences in secondary outcomes observed.
- Early sivelestat administration linked to reduced mortality.
Conclusions:
- Sivelestat use may reduce 28-day mortality in severe COVID-19 ICU patients.
- Sivelestat shows promise as a treatment for severe COVID-19.
Background:
The cytokine storm is a pivotal factor in the progression of coronavirus disease 2019 (COVID-19) to severe disease. Sivelestat, recognized for its anti-inflammatory properties, holds promise as a therapeutic intervention for patients with severe COVID-19.
Methods:
We conducted a multicenter, retrospective study involving patients admitted to the intensive care unit (ICU) with severe COVID-19 in China. A 1:2 propensity score matching (PSM) was employed to adjust for confounding factors and differences between the sivelestat and non-sivelestat groups.
Results:
Our analysis involved 2030 patients with severe COVID-19. After applying a 1:2 PSM ratio, the sivelestat group consisted of 115 patients, while the non-sivelestat group comprised 211 patients. The findings indicated that sivelestat administration was associated with enhanced survival rates at 28 days for patients with severe COVID-19 (53.55% vs. 40.87%; P = 0.03). However, no significant differences were noted in the secondary outcomes, which included ventilator-free days within 28 days, gastrointestinal bleeding, septic shock, acute myocardial injury, venous thrombosis, acute liver injury, and acute kidney injury. Furthermore, this study revealed that early administration of sivelestat could reduce patient mortality.
Conclusions:
Our study suggests that sivelestat use may be associated with reduced 28-day mortality in ICU patients with severe COVID-19.
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