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Efficacy of early sivelestat administration on acute lung injury and acute respiratory distress syndrome

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摘要:Background and objective:The efficacy of sivelestat, a neutrophil elastase inhibitor, for acute lung injury (ALI) and acute respiratory distress syndrome (ARDS) remains controversial. We investigated the role of sivelestat in ALI/ARDS patients on mortality as an end point between the sivelestat group and the non-sivelestat group within 7 days of admission. Methods:This study was performed using the Japanese nationwide administrative database (Diagnostic Procedure Combination; DPC) in 2012. We employed the propensity score weighting method with a Cox proportional hazards model to compare the mortality between the sivelestat group and the non-sivelestat group. Results:A total of 4276 patients were eligible for this study; 1997 patients were treated with sivelestat and 2279 patients did not receive sivelestat within 7 days of admission. After adjusting for confounds, the mortality within 3 months was significantly lower in the sivelestat group compared with the non-sivelestat group (weighted hazard ratio: 0.83; 95% CI: 0.75-0.93; P < 0.002). Multiple regression analysis revealed that younger age, absence of cancer, no need for haemodialysis and no use of high-dose methylprednisolone were significantly correlated with treatment success (survive). Conclusion:These results of this retrospective and observational study suggest that administration of sivelestat within 7 days of admission may improve the prognosis of patients with ALI/ARDS. To our knowledge, this is the largest study to evaluate the efficacy of sivelestat on ALI/ARDS. Keywords: acute lung injury; acute respiratory distress syndrome; inverse probability of treatment weighting; nationwide administrative database; sivelestat.
标签: ALI/ARDS 产品信息/适应症 汇伦医药 西维来司他钠 ICU 外科 内科 急诊 呼吸科
查看数:134
发布时间:2024-09-04 邹文成
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  • 附件1: ARDS10-Efficacy of early sivelestat administration on acute lung injury and.pdf 下载附件
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