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Exogenous pulmonary surfactant for the treatment of adult patients with acute respiratory distress syndrome: results of a meta-analysis

机译:外源性肺表面活性剂治疗成人急性呼吸窘迫综合征的患者:荟萃分析的结果

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IntroductionThe purpose of this study was to perform a systematic review and meta-analysis of exogenous surfactant administration to assess whether this therapy may be useful in adult patients with acute respiratory distress syndrome.MethodsWe performed a computerized literature search from 1966 to December 2005 to identify randomized clinical trials. The primary outcome measure was mortality 28–30 days after randomization. Secondary outcome measures included a change in oxygenation (PaO2:FiO2 ratio), the number of ventilation-free days, and the mean duration of ventilation. Meta-analysis was performed using the inverse variance method.ResultsTwo hundred and fifty-one articles were identified. Five studies met our inclusion criteria. Treatment with pulmonary surfactant was not associated with reduced mortality compared with the control group (odds ratio 0.97; 95% confidence interval (CI) 0.73, 1.30). Subgroup analysis revealed no difference between surfactant containing surface protein or not – the pooled odds ratio for mortality was 0.87 (95% CI 0.48, 1.58) for trials using surface protein and the odds ratio was 1.08 (95% CI 0.72, 1.64) for trials without surface protein. The mean difference in change in the PaO2:FiO2 ratio was not significant (P = 0.11). There was a trend for improved oxygenation in the surfactant group (pooled mean change 13.18 mmHg, standard error 8.23 mmHg; 95% CI -2.95, 29.32). The number of ventilation-free days and the mean duration of ventilation could not undergo pooled analysis due to a lack of sufficient data.ConclusionExogenous surfactant may improve oxygenation but has not been shown to improve mortality. Currently, exogenous surfactant cannot be considered an effective adjunctive therapy in acute respiratory distress syndrome.
机译:简介本研究的目的是对外源性表面活性剂的使用进行系统的回顾和荟萃分析,以评估该疗法是否可用于成人急性呼吸窘迫综合征患者。方法我们从1966年至2005年12月进行了计算机文献检索,以鉴定随机临床试验。主要结局指标是随机分组后28-30天的死亡率。次要结局指标包括氧合作用(PaO2:FiO2比)的变化,无通气天数和平均通气时间。结果采用逆方差法进行荟萃分析。结果鉴定了251篇文章。五项研究符合我们的纳入标准。与对照组相比,用肺表面活性剂治疗并没有降低死亡率(优势比为0.97; 95%置信区间(CI)为0.73,1.30)。亚组分析显示,含表面活性剂的表面蛋白与不含表面蛋白之间没有差异-使用表面蛋白的试验的死亡率综合优势比为0.87(95%CI 0.48,1.58),试验的优势比为1.08(95%CI 0.72,1.64)没有表面蛋白。 PaO2:FiO2比值变化的平均差异不显着(P = 0.11)。表面活性剂组有改善氧合的趋势(合并平均变化13.18 mmHg,标准误8.23 mmHg; 95%CI -2.95,29.32)。由于缺乏足够的数据,无法进行无通气天数和平均通气时间的汇总分析。结论外源性表面活性剂可能会改善氧合作用,但并未显示出可以提高死亡率。当前,外源性表面活性剂不能被认为是急性呼吸窘迫综合征的有效辅助疗法。

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