Sema Arayici, Gulsum Kadioglu Simsek, Birgul Say, Mehmet Yekta Oncel, Fatma Nur Sari, Nurdan Uras, Evrim Dizdar
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引用次数: 0
摘要
本研究旨在比较鼻持续气道正压通气(nCPAP)和双水平气道正压通气(BiPAP)在早产儿呼吸窘迫综合征(RDS)中的应用。早产儿(≤32孕周)在出生时被随机分为两个研究组:nCPAP或BiPAP。评估主要结局(前72小时内给予表面活性物质和无创呼吸支持失败)和次要结局(通气支持持续时间、气胸、支气管肺发育不良、动脉导管未闭、坏死性小肠结肠炎、脑室内出血、早产儿视网膜病变、总肠内喂养时间、住院时间和死亡率)。对188例RDS早产儿进行分析。平均胎龄分别为28.8±1.8周(nCPAP)和29±1.9周(BiPAP)。无创呼吸支持失败(25% vs 33%, RR: 0.74, 95% CI: 0.47-1.17)或表面活性剂治疗失败(35% vs 38%, RR: 0.92, 95% CI: 0.49-1.71)两组间无统计学差异。两组间的次要结局无显著差异。婴儿亚组分析
Nasal CPAP and BiPAP as the Initial Respiratory Support in Preterm Infants: A Randomized Controlled Trial.
This study aimed to compare the nasal continuous positive airway pressure (nCPAP) and bi-level positive airway pressure (BiPAP) in preterm infants with respiratory distress syndrome (RDS).Preterm infants (≤32 weeks of gestation) were randomly assigned, at birth, into two study groups: nCPAP or BiPAP. Primary outcomes (surfactant administration and failure of non-invasive respiratory support within the first 72 hours), and secondary outcomes (duration of ventilation support, pneumothorax, bronchopulmonary dysplasia, patent ductus arteriosus, necrotizing enterocolitis, intraventricular haemorrhage, retinopathy of prematurity, time to total enteral feeding, length of hospital stay, and mortality) were assessed.A total of 188 preterm infants with RDS were analysed. Mean gestational age was 28.8±1.8 weeks (nCPAP) versus 29±1.9 weeks (BiPAP). There were no statistically significant differences between groups in the failure of non-invasive respiratory support (25% vs. 33%, RR: 0.74, 95% CI: 0.47-1.17) or surfactant administration (35% vs. 38%, RR: 0.92, 95% CI: 0.49-1.71). No significant differences were observed in secondary outcomes between the two groups. Subgroup analysis of infants<30 weeks yielded similar results.Although two-level CPAP theoretically offers benefits, BiPAP was not superior to nCPAP as initial support in preterm infants with RDS. This underscores the continued value of the simpler, well-established nCPAP and the need for multicentre trials involving preterm infants of varying gestational ages.
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