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Randomised controlled trial of respiratory system compliancemeasurements in mechanically ventilated neonates

机译:呼吸系统顺应性的随机对照试验机械通气新生儿的测量

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摘要

AIM—To determine whether outcomes of neonatal mechanical ventilation could be improved by regular pulmonary function testing.
METHODS—Two hundred and forty five neonates, without immediately life threatening congenital malformations, were mechanically ventilated in the newborn period. Infants were randomly allocated to conventional clinical management (control group) or conventional management supplemented by regular measurements of static respiratory system compliance, using the single breath technique, with standardised management advice based on the results.
RESULTS—Fifty five (45%) infants in each group experienced one or more adverse outcomes. The median (quartile) durations of ventilation and oxygen supplementation were 5 (2-12) and 6 (2-34) days for the control group, and 4 (2-9) and 6 (3-36) days for the experimental group (not significant). On post-hoc secondary analysis, control group survivors were ventilated for 1269 days with a median (quartile) of 5 (2-13) days, and experimental group survivors were ventilated for 775 days with a median (quartile) duration of 3 (2-8) days (p=0.03).
CONCLUSIONS—Although primary analysis did not show any substantial benefit associated with regular measurement of static respiratory system compliance, this may reflect a type II error, and amoderate benefit has not been excluded. Larger studies are required toestablish the value of on-line monitoring techniques now available with neonatal ventilators.

机译:目的:确定定期进行肺功能检查是否可以改善新生儿机械通气的结果。
方法:在新生儿期,对无立即危及生命的先天性畸形的245例新生儿进行了机械通气。婴儿被随机分配到常规临床治疗组(对照组)或常规治疗,并通过单呼吸技术定期测量静态呼吸系统依从性,并根据结果制定标准化的治疗建议。
结果— 55(45)每组中有%)的婴儿经历了一个或多个不良后果。对照组的通气和增氧的中位(四分位数)持续时间分别为5(2-12)和6(2-34)天,实验组为4(2-9)和6(3-36)天(不重要)。在事后进行次要分析时,对照组幸存者通气1269天,中位(四分位数)为5(2-13)天,实验组幸存者通气775天,中位(四分位数)持续时间为3(2 -8)天(p = 0.03)。
结论—尽管主要分析并未显示出定期测量静态呼吸系统顺应性有任何实质性益处,但这可能反映了II型错误,并且没有排除中等利益。需要进行更大的研究建立新生儿呼吸机在线监测技术的价值。

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