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Three-year perinatal outcomes of less invasive beractant administration in preterm infants with respiratory distress syndrome

机译:早产儿患有呼吸窘迫综合征的早产儿

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Objective:To assess the impact of beractant treatment using the less invasive surfactant administration (LISA) technique on perinatal outcomes in a prospective cohort of preterm infants with respiratory distress syndrome (RDS). Design:Single-center prospective study conducted in a Department of Neonatology of a tertiary care university-affiliated hospital in Madrid, Spain. Methods:Preterm infants born at <31 + 6 weeks' gestation attended in the neonatal intensive care unit (NICU) between 2012 and 2016. The main outcome was the need of invasive mechanical ventilation during the first 3 days of life. Beractant (100 mg; 4 mL/kg) was administered using the intubation-surfactant-extubation (INSURE) method during 2012 and 2013, and using the LISA procedure between 2014 and 2016. Results:The study population included 512 infants, 232 in the first period and 280 in the second period. Mechanical ventilation exposure during hospitalization showed a significant reduction in the second study period, with an adjusted OR of 0.61, 95% CI 0.39-0.96. Also, an increase of free-bronchopulmonary dysplasia (BPD) survival was found (adjusted OR 2.14, 95% CI 1.29-3.55). These significant differences in perinatal outcomes were observed only in the group of infants of 26 + 0 to 28 + 6 gestational weeks. The success rate of the first dose of beractant using LISA regarding no need of intubation during the first 3 days of life was 54% increasing to 69% in the group of 26 + 0-28 + 6 weeks of gestation. The success rate regarding free-BPD survival was 63.5% in the whole series of LISA treated patients and 72.4% in the group of 26 + 0-28 + 6 weeks. Oxygen reduction after surfactant administration (OR 39.6, 95% CI 6.1-255.8,p < .001) was predictor of LISA success, whereas LISA failure was an independent factor for air leak (OR 18.92, 95% CI 1.31-272.32,p = .031) and Death or BPD outcome (OR 19.3, 95% IC 2.5-147.4,p = .004). Gestational age was inversely associated with the need of intubation after LISA (OR 0.53, 95% CI 0.32-0.87,p = .013). Conclusions:Beractant administration by LISA technique effective reduced the need of intubation during the first 3 days of life and was associated with an increase in survival-free BPD in the group of infants born at 26 + 0 and 28 + 6 weeks' gestation.
机译:目的:评估伯氏患者治疗伯氏患者治疗的影响,患有呼吸窘迫综合征(RDS)的前瞻性婴儿围困群体的围类结果。设计:西班牙马德里三级护理大学附属医院的新生儿学系中的单中心前瞻性研究。方法:2012年至2016年间新生儿重症监护单位(NICU)出生的早产儿出生于<31 + 6周的妊娠。主要结果是在生命的前3天内需要侵入机械通气。在2012年和2013年期间使用插管 - 表面活性剂 - 拔管(保险)方法给药(100mg; 4ml / kg),并使用2014年和2016年之间的LISA程序。结果:研究人群包括512名婴儿,232第二个时期的第一期和280。在住院期间机械通气暴露显示第二研究期间显着降低,调节或0.61,95%CI 0.39-0.96。此外,发现了自由支气管扩张发育不良(BPD)存活率(调节或2.14,95%CI 1.29-3.55)。仅在26 + 0至28 + 6个妊娠周的婴儿组中观察到围产期结果的这些显着差异。在寿命前3天内无需插管,使用丽莎使用丽莎的第一剂伯乳剂的成功率为54%,妊娠26 + 0-28 + 6周内增加69%。关于自由BPD存活的成功率在全系列丽莎治疗患者中为63.5%,72.4%,26 + 0-28 + 6周内。表面活性剂施用后的氧还原(或39.6,95%CI 6.1-255.8,P <.001)是LISA成功的预测因子,而丽莎失败是空气泄漏的独立因素(或18.92,95%CI 1.31-272.32,P = .031)和死亡或BPD结果(或19.3,95%IC 2.5-147.4,P = .004)。妊娠期患者与插管后的需要与插管(或0.53,95%CI 0.32-0.87,P = .013)相关。结论:衡产人员通过LISA技术的伯施工人在生命的前3天内有效降低了插管的需要,并且与在妊娠26 + 0和28 + 6周内出生的婴儿组中的存活BPD增加有关。

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