Bahadue Felicia L, Soll Roger
University of Vermont, Burlington, Vermont, USA.
Cochrane Database Syst Rev. 2012 Nov 14;11(11):CD001456. doi: 10.1002/14651858.CD001456.pub2.
Clinical trials have confirmed that surfactant therapy is effective in improving the immediate need for respiratory support and the clinical outcome of premature newborns. Trials have studied a wide variety of surfactant preparations used either to prevent (prophylactic or delivery room administration) or treat (selective or rescue administration) respiratory distress syndrome (RDS). Using either treatment strategy, significant reductions in the incidence of pneumothorax, as well as significant improvement in survival, have been noted. It is unclear whether there are any advantages to treating infants with respiratory insufficiency earlier in the course of RDS.
To compare the effects of early versus delayed selective surfactant therapy for newborns intubated for respiratory distress within the first two hours of life. Planned subgroup analyses included separate comparisons for studies utilizing natural surfactant extract and synthetic surfactant.
We searched the Oxford Database of Perinatal Trials, MEDLINE (MeSH terms: pulmonary surfactant; text word: early; limits: age, newborn: publication type, clinical trial), PubMed, abstracts, conference and symposia proceedings, expert informants, and journal handsearching in the English language. For the updated search in April 2012 we searched the Cochrane Central Register of Controlled Trials (CENTRAL, The Cochrane Library, 2012, Issue 1) and PubMed (January 1997 to April 2012).
Randomized and quasi-randomized controlled clinical trials comparing early selective surfactant administration (surfactant administration via the endotracheal tube in infants intubated for respiratory distress, not specifically for surfactant dosage) within the first two hours of life versus delayed selective surfactant administration to infants with established RDS were considered for review.
Data regarding clinical outcomes were excerpted from the reports of the clinical trials by the review authors. Subgroup analyses were performed based on type of surfactant preparation, gestational age, and exposure to prenatal steroids. Data analysis was performed in accordance with the standards of the Cochrane Neonatal Review Group.
Six randomized controlled trials met selection criteria. Two of the trials utilized synthetic surfactant (Exosurf Neonatal) and four utilized animal-derived surfactant preparations.The meta-analyses demonstrate significant reductions in the risk of neonatal mortality (typical risk ratio (RR) 0.84; 95% confidence interval (CI) 0.74 to 0.95; typical risk difference (RD) -0.04; 95% CI -0.06 to -0.01; 6 studies; 3577 infants), chronic lung disease (typical RR 0.69; 95% CI 0.55 to 0.86; typical RD -0.04; 95% CI -0.06 to -0.01; 3 studies; 3041 infants), and chronic lung disease or death at 36 weeks (typical RR 0.83; 95% CI 0.75 to 0.91; typical RD -0.06; 95% CI -0.09 to -0.03; 3 studies; 3050 infants) associated with early treatment of intubated infants with RDS.Intubated infants randomized to early selective surfactant administration also demonstrated a decreased risk of acute lung injury including a decreased risk of pneumothorax (typical RR 0.69; 95% CI 0.59 to 0.82; typical RD -0.05; 95% CI -0.08 to -0.03; 5 studies; 3545 infants), pulmonary interstitial emphysema (typical RR 0.60; 95% CI 0.41 to 0.89; typical RD -0.06; 95% CI -0.10 to -0.02; 3 studies; 780 infants), and overall air leak syndromes (typical RR 0.61; 95% CI 0.48 to 0.78; typical RD -0.18; 95% CI -0.26 to -0.09; 2 studies; 463 infants).A trend toward risk reduction for bronchopulmonary dysplasia (BPD) or death at 28 days was also evident (typical RR 0.94; 95% CI 0.88 to 1.00; typical RD -0.04; 95% CI -0.07 to -0.00; 3 studies; 3039 infants). No differences in other complications of RDS or prematurity were noted.Only two studies reported on infants under 30 weeks' gestation. Decreased risk of neonatal mortality and chronic lung disease or death at 36 weeks' postmenstrual age was noted.
AUTHORS' CONCLUSIONS: Early selective surfactant administration given to infants with RDS requiring assisted ventilation leads to a decreased risk of acute pulmonary injury (decreased risk of pneumothorax and pulmonary interstitial emphysema) and a decreased risk of neonatal mortality and chronic lung disease compared to delaying treatment of such infants until they develop worsening RDS.
临床试验已证实,表面活性剂疗法可有效改善早产新生儿对呼吸支持的即时需求及临床结局。多项试验研究了多种用于预防(预防性或产房给药)或治疗(选择性或挽救性给药)呼吸窘迫综合征(RDS)的表面活性剂制剂。采用任何一种治疗策略,均已注意到气胸发生率显著降低以及存活率显著提高。目前尚不清楚在RDS病程早期治疗呼吸功能不全的婴儿是否具有任何优势。
比较出生后两小时内因呼吸窘迫而插管的新生儿早期与延迟选择性表面活性剂治疗的效果。计划的亚组分析包括对使用天然表面活性剂提取物和合成表面活性剂的研究进行单独比较。
我们检索了牛津围产期试验数据库、MEDLINE(医学主题词:肺表面活性剂;文本词:早期;限制条件:年龄,新生儿;出版类型,临床试验)、PubMed、摘要、会议及专题讨论会论文集、专家提供的信息,并对英文期刊进行手工检索。在2012年4月的更新检索中,我们检索了Cochrane对照试验中心注册库(CENTRAL,Cochrane图书馆,2012年第1期)和PubMed(1997年1月至2012年4月)。
纳入随机和半随机对照临床试验进行综述,这些试验比较了出生后两小时内对因呼吸窘迫而插管的婴儿(并非专门针对表面活性剂剂量)进行早期选择性表面活性剂给药与对已确诊RDS的婴儿进行延迟选择性表面活性剂给药的效果。
综述作者从临床试验报告中摘录有关临床结局的数据。根据表面活性剂制剂类型、胎龄和产前使用类固醇情况进行亚组分析。数据分析按照Cochrane新生儿综述组的标准进行。
六项随机对照试验符合入选标准。其中两项试验使用合成表面活性剂(Exosurf Neonatal),四项试验使用动物源性表面活性剂制剂。荟萃分析表明,对插管的RDS婴儿进行早期治疗可显著降低新生儿死亡风险(典型风险比(RR)0.84;95%置信区间(CI)0.74至0.95;典型风险差(RD)-0.04;95%CI -0.06至-0.01;6项研究;3577例婴儿)、慢性肺病风险(典型RR 0.69;95%CI 0.55至0.86;典型RD -0.04;95%CI -0.06至-0.01;3项研究;3041例婴儿)以及36周时慢性肺病或死亡风险(典型RR 0.83;95%CI 0.75至0.91;典型RD -0.06;95%CI -0.09至-0.03;3项研究;3050例婴儿)。随机接受早期选择性表面活性剂给药的插管婴儿急性肺损伤风险也有所降低,包括气胸风险降低(典型RR 0.69;95%CI 0.59至0.82;典型RD -0.05;95%CI -0.08至-0.03;5项研究;3545例婴儿)、肺间质肺气肿风险降低(典型RR 0.60;95%CI 0.41至0.89;典型RD -0.06;95%CI -0.10至-0.02;3项研究;780例婴儿)以及总体气漏综合征风险降低(典型RR 0.61;95%CI 0.48至0.78;典型RD -0.18;95%CI -0.26至-0.09;2项研究;463例婴儿)。28天时支气管肺发育不良(BPD)或死亡风险也有降低趋势(典型RR 0.94;95%CI 0.88至1.00;典型RD -0.04;95%CI -0.07至-0.00;3项研究;3039例婴儿)。未发现RDS或早产的其他并发症存在差异。仅有两项研究报告了孕周小于30周的婴儿情况。观察到月经后36周时新生儿死亡风险以及慢性肺病或死亡风险降低。
与将患有RDS且需要辅助通气的婴儿的治疗延迟至其RDS病情恶化相比,早期选择性表面活性剂给药可降低急性肺损伤风险(气胸和肺间质肺气肿风险降低)以及新生儿死亡和慢性肺病风险。