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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Application of continuous positive airway pressure in the delivery room: a multicenter randomized clinical trial
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Application of continuous positive airway pressure in the delivery room: a multicenter randomized clinical trial

机译:持续气道正压在分娩室中的应用:多中心随机临床试验

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This study evaluated whether the use of continuous positive airway pressure (CPAP) in the delivery room alters the need for mechanical ventilation and surfactant during the first 5 days of life and modifies the incidence of respiratory morbidity and mortality during the hospital stay. The study was a multicenter randomized clinical trial conducted in five public university hospitals in Brazil, from June 2008 to December 2009. Participants were 197 infants with birth weight of 1000-1500 g and without major birth defects. They were treated according to the guidelines of the American Academy of Pediatrics (APP). Infants not intubated or extubated less than 15 min after birth were randomized for two treatments, routine or CPAP, and were followed until hospital discharge. The routine (n=99) and CPAP (n=98) infants studied presented no statistically significant differences regarding birth characteristics, complications during the prenatal period, the need for mechanical ventilation during the first 5 days of life (19.2 vs 23.4%, P=0.50), use of surfactant (18.2 vs 17.3% P=0.92), or respiratory morbidity and mortality until discharge. The CPAP group required a greater number of doses of surfactant (1.5 vs 1.0, P=0.02). When CPAP was applied to the routine group, it was installed within a median time of 30 min. We found that CPAP applied less than 15 min after birth was not able to reduce the need for ventilator support and was associated with a higher number of doses of surfactant when compared to CPAP applied as clinically indicated within a median time of 30 min.
机译:这项研究评估了在分娩室使用持续气道正压通气(CPAP)是否会在生命的前5天改变对机械通气和表面活性剂的需求,并改变住院期间呼吸系统疾病和死亡率的发生率。这项研究是一项多中心随机临床试验,于2008年6月至2009年12月在巴西的五所公立大学医院中进行。参与者为197例婴儿,出生体重1000-1500 g,无重大出生缺陷。根据美国儿科学会(APP)的指导对它们进行了治疗。出生后少于15分钟未插管或拔管的婴儿随机接受常规或CPAP两种治疗,并随访直至出院。研究的常规婴儿(n = 99)和CPAP(n = 98)在出生特征,产前并发症,出生后前5天对机械通气的需求方面无统计学差异(19.2 vs 23.4%,P = 0.50),使用表面活性剂(18.2 vs 17.3%P = 0.92)或呼吸道发病率和死亡率直至出院。 CPAP组需要更多剂量的表面活性剂(1.5对1.0,P = 0.02)。将CPAP应用于常规组后,将在30分钟的中值时间内安装它。我们发现,与30分钟中位临床应用的CPAP相比,出生后不到15分钟使用CPAP不能减少对呼吸机支持的需要,并且与更高剂量的表面活性剂有关。

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