Clinical evaluation of sivelestat for acute lung injury/acute respiratory distress syndrome following surgery for abdominal sepsis

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Abstract

Background: The efficacy of sivelestat in the treatment of acute lung injury/acute respiratory distress syndrome (ALI/ARDS) has not been established. In part, this is due to the wide variety of factors involved in the etiology of ALI/ARDS. In this study, we examined the efficacy of sivelestat in patients with ALI/ARDS associated with abdominal sepsis. Methods: The subjects were 49 patients with ALI/ARDS after surgery for abdominal sepsis. The efficacy of sivelestat was retrospectively assessed in two treatment groups, i.e., a sivelestat group (n = 34) and a non-sivelestat group (n = 15). Results: The sivelestat group showed signifcant improvements in oxygenation, thrombocytopenia, and multiple organ dysfunction score. The number of ventilator days (6.6 ± 6.1 versus 11.1 ± 8.4 days; P = 0.034) and length of stay in the intensive care unit (8.5 ± 6.2 versus 13.3 ± 9.5 days; P = 0.036) were signifcantly lower in the sivelestat group. The hospital mortality rate decreased by half in the sivelestat group, but was not signifcantly different between the two groups. Conclusion: Administration of sivelestat to patients with ALI/ARDS following surgery for abdominal sepsis resulted in early improvements of oxygenation and multiple organ dysfunction score, early ventilator weaning, and early discharge from the intensive care unit. © 2012 Tsuboko et al, publisher and licensee Dove Medical Press Ltd.

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Tsuboko, Y., Takeda, S., Mii, S., Nakazato, K., Tanaka, K., Uchida, E., & Sakamoto, A. (2012). Clinical evaluation of sivelestat for acute lung injury/acute respiratory distress syndrome following surgery for abdominal sepsis. Drug Design, Development and Therapy, 6, 273–278. https://doi.org/10.2147/DDDT.S36436

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