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Randomised controlled trial of respiratory system compliance measurements 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 neonatalmechanical ventilation could be improved by regular pulmonary function testing.
METHODS—Two hundred and forty five neonates,without immediately life threatening congenital malformations, weremechanically ventilated in the newborn period. Infants were randomlyallocated to conventional clinical management (control group) orconventional management supplemented by regular measurements of staticrespiratory system compliance, using the single breath technique, withstandardised management advice based on the results.
RESULTS—Fifty five (45%) infants in each groupexperienced one or more adverse outcomes. The median (quartile)durations of ventilation and oxygen supplementation were 5 (2-12) and6 (2-34) days for the control group, and 4 (2-9) and 6 (3-36) daysfor the experimental group (not significant). On post-hoc secondaryanalysis, control group survivors were ventilated for 1269 days with amedian (quartile) of 5 (2-13) days, and experimental group survivorswere ventilated for 775 days with a median (quartile) duration of 3 (2-8) days (p=0.03).
CONCLUSIONS—Although primary analysis did not showany substantial benefit associated with regular measurement of staticrespiratory 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-新生儿期机械通气,无立即危及生命的先天性畸形的245例新生儿。婴儿被随机分配到常规临床管理(对照组)或常规管理,辅以常规测量的静态呼吸系统顺应性,使用单次呼吸技术,并根据结果制定标准化的管理建议。结果-每组中有五十五(45%)婴儿经历了一个或多个不良后果。对照组的通气和氧气补充的中位(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(非重大)。事后进行二次分析,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与定期测量静呼吸系统依从性相关的任何实质性收益,但这可能反映出II型错误,并且并未排除中等收益。为了确定新生儿呼吸机现在可用的在线监测技术的价值,需要进行更大的研究。

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