Jat Kana R, Chawla Deepak
Department of Pediatrics, Government Medical College and Hospital, Chandigarh, India.
Cochrane Database Syst Rev. 2012 Sep 12(9):CD009194. doi: 10.1002/14651858.CD009194.pub2.
Bronchiolitis is one of the most frequent causes of respiratory failure in infants; some infants will require intensive care and mechanical ventilation. There is lack of evidence regarding effective treatment for bronchiolitis other than supportive care. Abnormalities of surfactant quantity or quality (or both) have been observed in severe cases of bronchiolitis. Exogenous surfactant administration appears to favourably change the haemodynamics of the lungs and may be a potentially promising therapy for severe bronchiolitis.
To evaluate the efficacy of exogenous surfactant administration (i.e. intratracheal administration of surfactant of any type (whether animal-derived or synthetic), at any dose and at any time after start of ventilation) compared to placebo, no intervention or standard care in reducing mortality and the duration of ventilation in infants and children with bronchiolitis requiring mechanical ventilation.
We searched CENTRAL 2012, Issue 4 which contains the Cochrane Acute Respiratory Infections Group's Specialised Register, MEDLINE (1948 to May week 1, 2012), EMBASE (1974 to May 2012), CINAHL (1982 to May 2012), LILACS (1985 to May 2012) and Web of Science (1985 to May 2012).
We considered prospective, randomised controlled trials (RCTs) and quasi-RCTs evaluating the effect of exogenous surfactant in infants and children with bronchiolitis requiring mechanical ventilation.
Two review authors selected studies independently. We extracted the data using a predefined proforma, independently analysed the data and performed meta-analyses.
We included three small RCTs enrolling 79 participants. Two trials did not use a placebo in the control arms and the third trial used air placebo. Two included studies did not describe mortality. We judged some of the included studies to have an unclear risk of bias but none of the included studies had a high risk of bias. Our pooled analysis of the three trials revealed that duration of mechanical ventilation was not different between the groups (mean difference (MD) -63.04, 95% confidence interval (CI) -130.43 to 4.35 hours) but duration of intensive care unit (ICU) stay was less in the surfactant group compared to the control group: MD -3.31 (95% CI -6.38 to -0.25 days). After excluding one trial which produced significant heterogeneity, the duration of mechanical ventilation and duration of ICU stay were significantly lower in the surfactant group compared to the control group: MD -28.99 (95% CI -40.10 to -17.87 hours) and MD -1.81 (95% CI -2.42 to -1.19 days), respectively. Use of surfactant had favourable effects on oxygenation and CO(2) elimination. No adverse effects and no complications were observed in any of the three included studies.
AUTHORS' CONCLUSIONS: The available evidence is insufficient to establish the effectiveness of surfactant therapy for bronchiolitis in critically ill infants who require mechanical ventilation. There is a need for larger trials with adequate power and a cost-effectiveness analysis to evaluate the effectiveness of exogenous surfactant therapy for infants with bronchiolitis who require intensive care management.
细支气管炎是婴儿呼吸衰竭最常见的病因之一;部分婴儿需要重症监护和机械通气。除支持治疗外,缺乏关于细支气管炎有效治疗方法的证据。在严重的细支气管炎病例中,已观察到表面活性物质数量或质量(或两者)异常。外源性表面活性物质给药似乎能有利地改变肺部血流动力学,可能是治疗严重细支气管炎的一种有潜在前景的疗法。
评估与安慰剂、不干预或标准治疗相比,外源性表面活性物质给药(即气管内给予任何类型的表面活性物质(无论是动物源性还是合成的),在通气开始后的任何剂量和任何时间)对需要机械通气的细支气管炎婴幼儿降低死亡率和缩短通气时间的疗效。
我们检索了2012年第4期的Cochrane系统评价数据库(CENTRAL),其中包含Cochrane急性呼吸道感染小组的专业注册库、医学期刊数据库(MEDLINE,1948年至2012年5月第1周)、荷兰医学文摘数据库(EMBASE,1974年至2012年5月)、护理学与健康领域数据库(CINAHL,1982年至2012年5月)、拉丁美洲和加勒比地区卫生科学数据库(LILACS,1985年至2012年5月)以及科学引文索引数据库(Web of Science,1985年至2012年5月)。
我们纳入了评估外源性表面活性物质对需要机械通气的细支气管炎婴幼儿疗效的前瞻性随机对照试验(RCT)和半随机对照试验。
两位综述作者独立选择研究。我们使用预定义的表格提取数据,独立分析数据并进行荟萃分析。
我们纳入了三项小型RCT,共79名参与者。两项试验在对照组中未使用安慰剂,第三项试验使用空气作为安慰剂。两项纳入研究未描述死亡率。我们判断部分纳入研究的偏倚风险不明确,但所有纳入研究均无高偏倚风险。我们对三项试验的汇总分析显示,两组间机械通气时间无差异(平均差(MD)-63.04,95%置信区间(CI)-为-130.43至4.35小时),但与对照组相比,表面活性物质组的重症监护病房(ICU)住院时间更短:MD -3.31(95% CI -6.38至-0.25天)。排除一项产生显著异质性的试验后,与对照组相比,表面活性物质组的机械通气时间和ICU住院时间显著缩短:MD分别为-28.99(95% CI -40.10至-17.87小时)和MD -1.81(95% CI -2.42至-1.19天)。表面活性物质的使用对氧合和二氧化碳清除有有利影响。三项纳入研究中均未观察到不良反应和并发症。
现有证据不足以确定表面活性物质疗法对需要机械通气的重症细支气管炎婴儿的有效性。需要进行更大规模、有足够效力的试验以及成本效益分析,以评估外源性表面活性物质疗法对需要重症监护管理的细支气管炎婴儿的有效性。