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

被引:45
作者
Meng, Haoyu [1 ,2 ]
Sun, Ying [2 ]
Lu, Jun [1 ]
Fu, Shukun [1 ]
Meng, Zhaoyi [3 ]
Scott, Melanie [4 ]
Li, Quan [1 ]
机构
[1] Tongji Univ, Sch Med, Dept Anesthesiol, Shanghai Peoples Hosp 10, Shanghai 200072, Peoples R China
[2] Nanjing Med Univ, Clin Med Coll 1, Nanjing, Jiangsu, Peoples R China
[3] Xinyi Peoples Hosp, Dept Surg, Xinyi, Jiangsu, Peoples R China
[4] Univ Pittsburgh, Dept Surg, Pittsburgh, PA USA
关键词
randomized control trial; PaO2:F1O2; exogenous surfactant; pulmonary surfactant; adverse effects; PROTEIN-C SURFACTANT; RECOMBINANT SURFACTANT; AEROSOLIZED SURFACTANT; THERAPY; ARDS; REPLACEMENT;
D O I
10.1053/j.jvca.2011.11.006
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
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. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:849 / 856
页数:8
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