Davidson Warren J, Dorscheid Del, Spragg Roger, Schulzer Michael, Mak Edwin, Ayas Najib T
Department of Medicine University of British Columbia, Vancouver, British Columbia, Canada.
Crit Care. 2006;10(2):R41. doi: 10.1186/cc4851.
The 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.
We 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.
Two 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.
Exogenous 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.
本研究的目的是对外源性表面活性剂给药进行系统评价和荟萃分析,以评估该疗法对成人急性呼吸窘迫综合征患者是否有用。
我们进行了一项计算机化文献检索,检索时间为1966年至2005年12月,以确定随机临床试验。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变化(动脉血氧分压:吸入氧分数值比值)、无通气天数以及平均通气持续时间。采用逆方差法进行荟萃分析。
共识别出251篇文章。五项研究符合我们的纳入标准。与对照组相比,肺表面活性剂治疗并未降低死亡率(优势比0.97;95%置信区间[CI] 0.73, 1.30)。亚组分析显示,含表面蛋白的表面活性剂与不含表面蛋白的表面活性剂之间无差异——使用表面蛋白的试验中,死亡率的合并优势比为0.87(95% CI 0.48, 1.58),未使用表面蛋白的试验中优势比为1.08(95% CI 0.72, 1.64)。动脉血氧分压:吸入氧分数值比值的变化均值差异无统计学意义(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)。由于缺乏足够数据,无通气天数和平均通气持续时间无法进行合并分析。
外源性表面活性剂可能改善氧合,但尚未显示能改善死亡率。目前,外源性表面活性剂不能被视为急性呼吸窘迫综合征的有效辅助治疗方法。