4.7 Article

A Randomized Clinical Trial of Hydroxymethylglutaryl-Coenzyme A Reductase Inhibition for Acute Lung Injury (The HARP Study)

出版社

AMER THORACIC SOC
DOI: 10.1164/rccm.201003-0423OC

关键词

simvastatin; acute lung injury; acute respiratory distress syndrome

资金

  1. HSC R&D Division, Public Health Agency Northern Ireland
  2. REVIVE
  3. Vectura
  4. Gilead
  5. GlaxoSmithKline
  6. AstraZeneca
  7. Public Health Agency [EAT/3180/05, CDV/3778/08] Funding Source: researchfish

向作者/读者索取更多资源

Rationale There is no effective pharmacological treatment for acute lung injury (All). Statins are a potential new therapy because they modify many of the underlying processes important in ALI. Objectives: To test whether simvastatin improves physiological and biological outcomes in ALI. Methods: We conducted a randomized, double-blinded, placebo-controlled trial in patients with ALL Patients received 80 mg simvastatin or placebo until cessation of mechanical ventilation or up to 14 days. Extravascular lung water was measured using thermodilution. Measures of pulmonary and nonpulmonary organ function were assessed daily. Pulmonary and systemic inflammation was assessed by bronchoalveolar lavage fluid and plasma cytokines. Systemic inflammation was also measured by plasma C-reactive protein. Measurements and Main Results: Sixty patients were recruited. Baseline characteristics, including demographics and severity of illness scores, were similar in both groups. At Day 7, there was no difference in extravascular lung water. By Day 14, the simvastatin-treated group had improvements in nonpulmonary organ dysfunction. Oxygenation and respiratory mechanics improved, although these parameters failed to reach statistical significance. Intensive care unit mortality was 30% in both groups. Simvastatin was well tolerated, with no increase in adverse events. Simvastatin decreased bronchoalveolar lavage IL-8 by 2.5-fold (P = 0.04). Plasma C-reactive protein decreased in both groups but failed to achieve significance in the placebo-treated group. Conclusions: Treatment with simvastatin appears to be safe and may be associated with an improvement in organ dysfunction in ALI. These clinical effects may be mediated by a reduction in pulmonary and systemic inflammation.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据