Late surfactant administration after 48 hours of age in preterm neonates with respiratory insufficiency: a systematic review and meta-analysis

Gonzalo Solís-García, Sara Elias, Michael Dunn, Bonny Jasani
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Abstract

Objective To systematically review and meta-analyse the effect of late surfactant administration versus placebo in reducing the incidence of death or bronchopulmonary dysplasia (BPD) in preterm infants. Design PubMed, EMBASE, CINAHL and Cochrane CENTRAL were searched until 30 May 2023, for randomised controlled trials (RCTs) comparing administration of surfactant after 48 hours of age versus placebo in preterm ventilator-dependent neonates. The primary outcome was incidence of death or BPD at 36 weeks’ postmenstrual age (PMA). Secondary outcomes included incidence of BPD at 36 weeks PMA, pre-discharge mortality, use of postnatal steroids, post-discharge respiratory support, treatment with steroids or hospitalisation prior to 1-year corrected age. Results Pooled analyses of four RCTs (N=850) showed no statistically significant difference between groups in the incidence of death or BPD at 36 weeks’ PMA (relative risk (RR) 0.99; 95% CI 0.90 to 1.10; Grades of Recommendation, Assessment, Development and Evaluation (GRADE): moderate). Late surfactant administration significantly decreased the need for post-discharge respiratory support prior to 1-year corrected age (two RCTs; N=522; RR 0.72; 95% CI 0.59 to 0.89; GRADE: low). Other secondary outcomes did not differ significantly between the groups. Conclusions Administration of late surfactant does not improve the rates of death or BPD at 36 weeks when administered to preterm infants with prolonged respiratory insufficiency. Additional adequately powered trials are needed to establish the efficacy of late surfactant therapy in preterm infants. PROSPERO registration number CRD42023432463.
呼吸功能不全早产儿48小时后给予表面活性剂:一项系统回顾和荟萃分析
目的系统回顾和荟萃分析表面活性剂晚期给药与安慰剂在降低早产儿死亡或支气管肺发育不良(BPD)发生率方面的效果。检索PubMed、EMBASE、CINAHL和Cochrane CENTRAL,直到2023年5月30日,以比较48小时后给药表面活性剂与安慰剂对依赖呼吸机的早产儿的随机对照试验(rct)。主要终点是经后36周(PMA)死亡或BPD的发生率。次要结局包括PMA 36周时BPD的发生率、出院前死亡率、产后类固醇的使用、出院后呼吸支持、类固醇治疗或1岁前的住院治疗。结果4项随机对照试验(N=850)的合并分析显示,36周PMA时两组患者的死亡或BPD发生率无统计学差异(相对危险度(RR) 0.99;95% CI 0.90 ~ 1.10;推荐、评估、发展和评估等级(GRADE):中等。晚期给药表面活性剂显著降低1岁矫正年龄前对出院后呼吸支持的需求(2项随机对照试验;N = 522;RR 0.72;95% CI 0.59 ~ 0.89;等级:低)。其他次要结果在两组间无显著差异。结论对于延长呼吸功能不全的早产儿,给予晚期表面活性剂并不能改善36周时的死亡率或BPD。需要更多的充分有力的试验来确定晚期表面活性剂治疗早产儿的疗效。普洛斯彼罗注册号CRD42023432463。如有合理要求,可提供资料。
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