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

Respirology. 2017 May;22(4):708-713. doi: 10.1111/resp.12969. Epub 2016 Dec 18.

Abstract

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.

Publication types

  • Multicenter Study
  • Observational Study

MeSH terms

  • Acute Lung Injury / drug therapy*
  • Aged
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Female
  • Follow-Up Studies
  • Glycine / administration & dosage
  • Glycine / analogs & derivatives*
  • Humans
  • Male
  • Prognosis
  • Respiratory Distress Syndrome / drug therapy*
  • Retrospective Studies
  • Serine Proteinase Inhibitors / administration & dosage
  • Sulfonamides / administration & dosage*
  • Time Factors
  • Treatment Outcome

Substances

  • Serine Proteinase Inhibitors
  • Sulfonamides
  • sivelestat
  • Glycine