Division of Neonatology, Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.
Pediatrics. 2011 Nov;128(5):e1069-76. doi: 10.1542/peds.2010-3848. Epub 2011 Oct 24.
We designed a multicenter randomized trial to compare 3 approaches to the initial respiratory management of preterm neonates: prophylactic surfactant followed by a period of mechanical ventilation (prophylactic surfactant [PS]); prophylactic surfactant with rapid extubation to bubble nasal continuous positive airway pressure (intubate-surfactant-extubate [ISX]) or initial management with bubble continuous positive airway pressure and selective surfactant treatment (nCPAP).
DESIGN/METHODS: Neonates born at 26 0/7 to 29 6/7 weeks' gestation were enrolled at participating Vermont Oxford Network centers and randomly assigned to PS, ISX, or nCPAP groups before delivery. Primary outcome was the incidence of death or bronchopulmonary dysplasia (BPD) at 36 weeks' postmenstrual age.
648 infants enrolled at 27 centers. The study was halted before the desired sample size was reached because of declining enrollment. When compared with the PS group, the relative risk of BPD or death was 0.78 (95% confidence interval: 0.59-1.03) for the ISX group and 0.83 (95% confidence interval: 0.64-1.09) for the nCPAP group. There were no statistically significant differences in mortality or other complications of prematurity. In the nCPAP group, 48% were managed without intubation and ventilation, and 54% without surfactant treatment.
Preterm neonates were initially managed with either nCPAP or PS with rapid extubation to nCPAP had similar clinical outcomes to those treated with PS followed by a period of mechanical ventilation. An approach that uses early nCPAP leads to a reduction in the number of infants who are intubated and given surfactant.
我们设计了一项多中心随机试验,比较了 3 种方法对早产儿初始呼吸管理的效果:预防性使用表面活性剂后进行一段时间的机械通气(预防性表面活性剂[PS]);预防性使用表面活性剂后快速拔管至鼻塞持续气道正压通气(插管-表面活性剂-拔管[ISX]),或初始采用鼻塞持续气道正压通气并选择性使用表面活性剂治疗(nCPAP)。
方法/设计:在参与的佛蒙特牛津网络中心,招募胎龄 26 0/7 至 29 6/7 周的新生儿,并在分娩前随机分配至 PS、ISX 或 nCPAP 组。主要结局为校正胎龄 36 周时的死亡率或支气管肺发育不良(BPD)发生率。
27 个中心共纳入 648 例婴儿。由于入组人数减少,该研究在达到预期样本量之前提前停止。与 PS 组相比,ISX 组的 BPD 或死亡相对风险为 0.78(95%置信区间:0.59-1.03),nCPAP 组为 0.83(95%置信区间:0.64-1.09)。死亡率或其他早产儿并发症无统计学差异。在 nCPAP 组中,48%的患儿无需插管和通气,54%无需表面活性剂治疗。
早产儿最初可采用 nCPAP 或 PS 治疗,PS 治疗后快速拔管至 nCPAP 与 PS 治疗后进行一段时间的机械通气的临床结局相似。早期采用 nCPAP 的方法可减少插管和使用表面活性剂的患儿数量。