Soll Roger, Ozek Eren
Division of Neonatal-Perinatal Medicine, University of Vermont, Fletcher Allen Health Care, Smith 552A, 111 Colchester Avenue, Burlington, Vermont, USA, 05401.
Cochrane Database Syst Rev. 2010 Jan 20;2010(1):CD001079. doi: 10.1002/14651858.CD001079.pub2.
Respiratory distress syndrome (RDS) is caused by a deficiency or dysfunction of pulmonary surfactant. A variety of surfactant products including protein free synthetic surfactant have been developed and tested in the prevention and treatment of RDS.
To assess the effect of prophylactic administration of protein free synthetic surfactant (SS) on mortality, chronic lung disease and other morbidities associated with prematurity in preterm newborns at risk for developing RDS. Subgroup analysis were planned according to the degree of prematurity, surfactant product and dosage schedule.
Searches were made of the The Cochrane Library, MEDLINE, OVID, EMBASE, CINAHL from 1966 to 2009. In addition, previous reviews including cross references and abstracts from the Society for Pediatric Research were searched. No language restrictions were applied.
Randomized and quasi-randomized controlled trials that compared the effect of protein free SS administered to high risk preterm newborns at or shortly after birth in order to prevent RDS, mortality and complications of prematurity.
Data regarding clinical outcomes was excerpted from the clinical trials by the reviewers. Data were analyzed according to the standards of the Cochrane Neonatal Review Group.
Studies of prophylactic administration of protein free SS note a variable improvement in the respiratory status and a decrease in respiratory distress syndrome in infants who receive prophylactic protein free SS. The meta-analysis supports a decrease in the risk of pneumothorax (typical relative risk 0.67, 95% CI 0.50, 0.90), pulmonary interstitial emphysema (typical relative risk 0.68, 95% CI 0.50, 0.93), and neonatal mortality (typical relative risk 0.70, 95% CI 0.58, 0.85). No differences were seen in the risk of intraventricular hemorrhage, necrotizing enterocolitis, bronchopulmonary dysplasia, retinopathy of prematurity and cerebral palsy. The meta-analysis supports an increase in the risk of patent ductus arteriosus associated with prophylactic SS administration (typical relative risk 1.11, 95% CI 1.00, 1.22), and an increase in the risk of pulmonary hemorrhage (typical relative risk 3.28, 95% CI 1.50, 7.16).
AUTHORS' CONCLUSIONS: Prophylactic intratracheal administration of protein free synthetic surfactant to infants at risk of developing respiratory distress syndrome has been demonstrated to improve clinical outcome. Infants who receive prophylactic protein free SS have a decreased risk of pneumothorax, a decreased risk of pulmonary interstitial emphysema, and a decreased risk of neonatal mortality. Infants who receive prophylactic protein free SS have an increased risk of developing patent ductus arteriosus and pulmonary hemorrhage.
呼吸窘迫综合征(RDS)由肺表面活性物质缺乏或功能障碍引起。多种表面活性物质产品,包括无蛋白合成表面活性物质,已被研发并用于RDS的预防和治疗试验。
评估预防性给予无蛋白合成表面活性物质(SS)对有发生RDS风险的早产新生儿死亡率、慢性肺病及其他与早产相关疾病的影响。计划根据早产程度、表面活性物质产品及给药方案进行亚组分析。
检索了1966年至2009年的考克兰图书馆、医学期刊数据库(MEDLINE)、OVID、荷兰医学文摘数据库(EMBASE)、护理学与健康领域数据库(CINAHL)。此外,还检索了既往综述,包括儿科研究学会的交叉参考文献和摘要。未设语言限制。
随机和半随机对照试验,比较出生时或出生后不久给予高危早产新生儿无蛋白SS以预防RDS、死亡率和早产并发症的效果。
评审人员从临床试验中摘录有关临床结局的数据。数据根据考克兰新生儿综述组的标准进行分析。
关于预防性给予无蛋白SS的研究表明,接受预防性无蛋白SS的婴儿呼吸状况有不同程度改善,呼吸窘迫综合征减少。荟萃分析支持气胸风险降低(典型相对风险0.67,95%可信区间0.50,0.90)、肺间质气肿风险降低(典型相对风险0.68,95%可信区间0.50,0.93)以及新生儿死亡率降低(典型相对风险0.70,95%可信区间0.58,0.85)。在脑室内出血、坏死性小肠结肠炎、支气管肺发育不良、早产儿视网膜病变和脑瘫风险方面未发现差异。荟萃分析支持预防性给予SS会增加动脉导管未闭风险(典型相对风险1.11,95%可信区间1.00,1.22)以及肺出血风险增加(典型相对风险3.28,95%可信区间1.50,7.16)。
已证明对有发生呼吸窘迫综合征风险的婴儿预防性气管内给予无蛋白合成表面活性物质可改善临床结局。接受预防性无蛋白SS的婴儿气胸风险降低、肺间质气肿风险降低、新生儿死亡率降低。接受预防性无蛋白SS的婴儿发生动脉导管未闭和肺出血的风险增加。