4.2 Article

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

Journal

JOURNAL OF CARDIOTHORACIC AND VASCULAR ANESTHESIA
Volume 26, Issue 5, Pages 849-856

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.jvca.2011.11.006

Keywords

randomized control trial; PaO2:F1O2; exogenous surfactant; pulmonary surfactant; adverse effects

Funding

  1. Shanghai Natural Science Foundation [10411951400, 11ZR1428100]
  2. Shanghai Tenth People's Hospital (5810 Project) [10RD204]

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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. (C) 2012 Elsevier Inc. All rights reserved.

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