首页> 外文期刊>Journal of cardiothoracic and vascular anesthesia >Exogenous surfactant may improve oxygenation but not mortality in adult patients with acute lung injury/acute respiratory distress syndrome: A meta-analysis of 9 clinical trials
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Exogenous surfactant may improve oxygenation but not mortality in adult patients with acute lung injury/acute respiratory distress syndrome: A meta-analysis of 9 clinical trials

机译:外源性表面活性剂可改善成年急性肺损伤/急性呼吸窘迫综合征患者的氧合作用,但不能改善死亡率:9项临床试验的荟萃分析

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Objective: To evaluate whether exogenous surfactant therapy may be useful in adult patients with acute lung injury or acute respiratory distress syndrome, using a meta-analysis of published clinical trials. Design: A comprehensive literature search was performed to identify all randomized clinical trials examining the effects of the treatment of acute lung injury/acute respiratory distress syndrome with exogenous surfactant in adults. The primary outcome measurement was mortality 28 or 30 days after randomization. Secondary outcome measurements included a change in the ratio of the partial pressure of arterial oxygen to the fraction of inspired oxygen in the first 24 hours or after 120 hours, the number of ventilation-free days, and any adverse effects. The meta-analysis was performed using the Review Manager 5.0.0 system. Participants: Randomized clinical trials. Intervention: Meta-analysis of 9 trials. Measurements and Main Results: Nine trials involving 2,575 patients were included in the meta-analysis. The analysis showed that treatment with exogenous pulmonary surfactant does not decrease mortality significantly. There was a significant effect of exogenous surfactant treatment on the change in the partial pressure of arterial oxygen/fraction of inspired oxygen ratio in the first 24 hours but this was lost by 120 hours. The duration of ventilation trended lower in surfactant-treated patients but this was not significant. In addition, surfactant-treated patients had a significantly higher risk of adverse effects. Conclusions: An exogenous surfactant may improve oxygenation over the first 24 hours after administration. However, treatment does not improve mortality and oxygenation over <120 hours after administration and results in a high rate of adverse effects. Therefore, the present data suggest that an exogenous surfactant cannot be considered an effective adjunctive therapy in patients with acute lung injury/acute respiratory distress syndrome.
机译:目的:使用已发表的临床试验的荟萃分析,评估外源性表面活性剂治疗对成年急性肺损伤或急性呼吸窘迫综合征患者是否有用。设计:进行了全面的文献检索,以鉴定所有使用外源性表面活性剂治疗成人急性肺损伤/急性呼吸窘迫综合征的疗效的随机临床试验。主要结局指标为随机分组后28或30天的死亡率。次要结果测量包括在前24小时或120小时后动脉血氧分压与吸入氧分率的比值变化,无通气天数以及任何不利影响。使用Review Manager 5.0.0系统进行荟萃分析。参加者:随机临床试验。干预:9项试验的荟萃分析。测量和主要结果:荟萃分析包括9项涉及2,575例患者的试验。分析表明,用外源性肺表面活性剂治疗不会显着降低死亡率。在最初的24小时内,外源性表面活性剂处理对动脉血氧分压/吸入氧分率的变化有显着影响,但在120小时后消失。在接受表面活性剂治疗的患者中,通气时间倾向于降低,但这并不明显。另外,用表面活性剂治疗的患者有明显更高的不良反应风险。结论:外源性表面活性剂可在给药后的最初24小时内改善氧合作用。但是,在给药后不到120小时内,治疗无法改善死亡率和氧合作用,并导致较高的不良反应率。因此,本数据表明,在患有急性肺损伤/急性呼吸窘迫综合征的患者中,不能认为外源性表面活性剂是有效的辅助治疗。

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