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他汀类药物治疗对呼吸机相关性肺炎患者死亡率的影响:一项随机临床试验。

Effect of statin therapy on mortality in patients with ventilator-associated pneumonia: a randomized clinical trial.

机构信息

Assistance Publique-Hôpitaux de Marseille, Hôpital Nord, Réanimation des Détresses Respiratoires et des Infections Sévères UMR-CNRS 7278, Aix-Marseile Université, Marseille, France.

出版信息

JAMA. 2013 Oct 23;310(16):1692-700. doi: 10.1001/jama.2013.280031.

Abstract

IMPORTANCE

Observational studies have reported that statin use may be associated with improved outcomes of various infections. Ventilator-associated pneumonia (VAP) is the most common infection in the intensive care unit (ICU) and is associated with substantial mortality.

OBJECTIVE

To determine whether statin therapy can decrease day-28 mortality in patients with VAP.

DESIGN, SETTING, AND PARTICIPANTS: Randomized, placebo-controlled, double-blind, parallel-group, multicenter trial performed in 26 intensive care units in France from January 2010 to March 2013. For power to detect an 8% absolute reduction in the day-28 mortality rate, we planned to enroll 1002 patients requiring invasive mechanical ventilation for more than 2 days and having suspected VAP, defined as a modified Clinical Pulmonary Infection Score of 5 or greater. The futility stopping rules were an absolute increase in day-28 mortality of at least 2.7% with simvastatin compared with placebo after enrollment of the first 251 patients.

INTERVENTIONS

Participants were randomized to receive simvastatin (60 mg) or placebo, started on the same day as antibiotic therapy and given until ICU discharge, death, or day 28, whichever occurred first.

MAIN OUTCOMES AND MEASURES

Primary outcome was day-28 mortality. Day-14, ICU, and hospital mortality rates were determined, as well as duration of mechanical ventilation and Sequential Organ Failure Assessment (SOFA) scores on days 3, 7, and 14.

RESULTS

The study was stopped for futility at the first scheduled interim analysis after enrollment of 300 patients, of whom all but 7% in the simvastatin group and 11% in the placebo group were naive to statin therapy at ICU admission. Day-28 mortality was not lower in the simvastatin group (21.2% [95% CI, 15.4% to 28.6%) than in the placebo group (15.2% [95% CI, 10.2% to 22.1%]; P = .10; hazard ratio, 1.45 [95% CI, 0.83 to 2.51]); the between-group difference was 6.0% (95% CI, -3.0% to 14.9%). In statin-naive patients, day-28 mortality was 21.5% (95% CI, 15.4% to 29.1%) with simvastatin and 13.8% (95% CI, 8.8% to 21.0%) with placebo (P = .054) (between-group difference, 7.7% [95%CI, -1.8% to 16.8%). There were no significant differences regarding day-14, ICU, or hospital mortality rates; duration of mechanical ventilation; or changes in SOFA score.

CONCLUSIONS AND RELEVANCE

In adults with suspected VAP, adjunctive simvastatin therapy compared with placebo did not improve day-28 survival. These findings do not support the use of statins with the goal of improving VAP outcomes.

TRIAL REGISTRATION

clinicaltrials.gov Identifier: NCT01057758.

摘要

重要性

观察性研究报告称,他汀类药物的使用可能与各种感染的改善结局相关。呼吸机相关性肺炎(VAP)是重症监护病房(ICU)最常见的感染,与大量死亡相关。

目的

确定他汀类药物治疗是否可以降低 VAP 患者的 28 天死亡率。

设计、地点和参与者:2010 年 1 月至 2013 年 3 月在法国 26 个重症监护病房进行的随机、安慰剂对照、双盲、平行组、多中心试验。为了有足够的统计学效力来检测 28 天死亡率降低 8%的绝对差值,我们计划招募 1002 名需要超过 2 天的有创机械通气且疑似患有 VAP 的患者,VAP 的定义为改良临床肺部感染评分(CPIS)为 5 或更高。无效性停止规则是与安慰剂相比,辛伐他汀治疗后第 251 例患者入组后第 28 天的死亡率绝对增加至少 2.7%。

干预措施

参与者被随机分配接受辛伐他汀(60mg)或安慰剂,在开始抗生素治疗的同一天开始治疗,持续使用至 ICU 出院、死亡或第 28 天,以先发生者为准。

主要结局和测量指标

主要结局是 28 天死亡率。确定了第 14 天、ICU 和医院的死亡率,以及机械通气时间和第 3、7 和 14 天的序贯器官衰竭评估(SOFA)评分。

结果

在招募了 300 名患者后,按计划进行了第一次中期分析,研究因无效而停止,辛伐他汀组所有患者(除 7%外)和安慰剂组所有患者(除 11%外)在入 ICU 时均未接受过他汀类药物治疗。与安慰剂组(15.2%[95%CI,10.2%至 22.1%])相比,辛伐他汀组(21.2%[95%CI,15.4%至 28.6%])的 28 天死亡率并没有更低(P=0.10;风险比,1.45[95%CI,0.83 至 2.51]);两组间的差异为 6.0%(95%CI,-3.0%至 14.9%)。在他汀类药物治疗初治患者中,辛伐他汀组的 28 天死亡率为 21.5%(95%CI,15.4%至 29.1%),安慰剂组为 13.8%(95%CI,8.8%至 21.0%)(P=0.054)(两组间差异,7.7%[95%CI,-1.8%至 16.8%])。两组在第 14 天、ICU 和医院的死亡率、机械通气时间或 SOFA 评分的变化方面没有显著差异。

结论和相关性

在疑似患有 VAP 的成年人中,与安慰剂相比,辛伐他汀辅助治疗并未改善 28 天生存率。这些发现不支持使用他汀类药物来改善 VAP 结局。

试验注册

clinicaltrials.gov 标识符:NCT01057758。

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