Soll R F, Dargaville P
Department of Pediatrics, University of Vermont College of Medicine, A-121 Medical Alumni Building, Burlington, Vermont 05405-0068, USA.
Cochrane Database Syst Rev. 2000(2):CD002054. doi: 10.1002/14651858.CD002054.
To evaluate the effect of surfactant administration in the treatment of term infants with meconium aspiration syndrome.
Searches were made using Medline (1985 to January 2000) (MeSH terms: pulmonary surfactant and meconium aspiration; limits: age groups, newborns; publication type, clinical trials), previous reviews including cross-references, abstracts, conference and symposia proceedings, expert informants, and journal hand searching in the English language. Authors were directly contacted to provide additional data.
Randomized controlled trials which evaluated the effect of surfactant administration in term infants with meconium aspiration syndrome are included in the analysis.
Data regarding clinical outcomes including duration of assisted ventilation, duration of supplemental oxygen, pneumothorax, intraventricular hemorrhage (any grade and severe IVH), chronic lung disease, treatment with extracorporeal membrane oxygenation (ECMO), and mortality were excerpted from the reports of the clinical trails by the reviewers. Data analysis was done in accordance with the standards of the Cochrane Neonatal Review Group.
Two randomized controlled trials met inclusion criteria. Findlay (1996) reports a decrease in the risk of pneumothorax (relative risk 0.09, 95% CI 0.01, 1.54, risk difference -0.25, 95% CI -0.45, -0.05). Both Findlay (1996) and Lotze (1998) report a decrease in the number of infants receiving extracorporeal membrane oxygenation. The meta-analysis supports a significant reduction in the risk of requiring extracorporeal membrane oxygenation (typical relative risk 0.64, 95% CI 0.46, 0.91 typical risk difference -0.17, 95% CI -0.30, -0.04). No difference was noted in overall mortality (typical relative risk 1.86 95% CI 0.35, 9.89, typical risk difference 0.02 95% CI -0.03, 0.07).
REVIEWER'S CONCLUSIONS: In infants with meconium aspiration syndrome, surfactant administration may reduce the severity of respiratory illness and decrease the number of infants with progressive respiratory failure requiring support with ECMO. The relative efficacy of surfactant therapy compared to, or in conjunction with, other approaches to treatment including inhaled nitric oxide, liquid ventilation, and high frequency ventilation remains to be tested.
评估表面活性剂治疗足月儿胎粪吸入综合征的效果。
利用Medline(1985年至2000年1月)进行检索(医学主题词:肺表面活性剂和胎粪吸入;限定条件:年龄组,新生儿;出版物类型,临床试验),检索既往综述,包括交叉参考文献、摘要、会议和专题讨论会记录、专家提供的信息,并手工检索英文期刊。直接联系作者以获取更多数据。
纳入分析评估表面活性剂治疗足月儿胎粪吸入综合征效果的随机对照试验。
评审员从临床试验报告中摘录有关临床结局的数据,包括辅助通气时间、补充氧气时间、气胸、脑室内出血(任何级别和重度脑室内出血)、慢性肺部疾病、体外膜肺氧合(ECMO)治疗及死亡率。数据分析按照Cochrane新生儿综述组的标准进行。
两项随机对照试验符合纳入标准。Findlay(1996年)报告气胸风险降低(相对风险0.09,95%可信区间0.01,1.54,风险差值-0.25,95%可信区间-0.45,-0.05)。Findlay(1996年)和Lotze(1998年)均报告接受体外膜肺氧合的婴儿数量减少。荟萃分析支持需要体外膜肺氧合的风险显著降低(典型相对风险0.64,95%可信区间0.46,0.91;典型风险差值-0.17,95%可信区间-0.30,-0.04)。总体死亡率未见差异(典型相对风险1.86,95%可信区间0.35,9.89;典型风险差值0.02,95%可信区间-0.03,0.07)。
在胎粪吸入综合征婴儿中,表面活性剂治疗可能降低呼吸疾病的严重程度,并减少需要体外膜肺氧合支持的进行性呼吸衰竭婴儿数量。表面活性剂治疗与包括吸入一氧化氮、液体通气和高频通气在内的其他治疗方法相比或联合使用的相对疗效仍有待检验。