(支气管肺的发育不良。在1984年至1988年间出生的88名儿童中进行了为期3年的研究。

Archives francaises de pediatrie Pub Date : 1993-08-01
D Valleur-Masson, M Vodovar, J Zeller, F Laudat, Y Masson, M Kassis, R Nobre, F Kochert, M Voyer
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引用次数: 0

摘要

背景:婴儿支气管肺发育不良(BD)的生存和预后取决于患者的成熟度、BD的严重程度和营养问题。本研究评估慢性肺衰竭在BD恢复期婴儿生长发育中的特殊作用。人群与方法:研究了1984年1月至1988年12月收治的88例BD患儿,他们的胎龄在25 ~ 41周5天(平均29周),出生体重在680 ~ 3400 g(平均1195)。所有患儿给予呼吸支持6 ~ 914天(平均84天),氧疗28 ~ 1232天(平均119天)。29名婴儿给予皮质类固醇治疗超过1个月。将80名胎龄小于33周的婴儿与272名相同胎龄但未患双相障碍的婴儿在第28天的结果进行比较。两组婴儿在2岁时进行检查,并分类为:a)残疾(神经缺陷、智商< 80、听力丧失、失明、抽搐);B)怀疑(短暂性神经功能障碍);c)正常。结果:88例28日龄婴儿中,19例在2岁前死亡;64例存活至2岁的婴儿中,16例为残疾,13例为可疑,35例正常。更重要的神经发育障碍危险因素是:a)脑超声检查显示有脑孔畸形和/或心室扩张;b)住院结束时头围< -2 SD;C)氧疗及住院> 5-6个月。在孕龄> 31-32周时,患有双相障碍的婴儿死亡率更高(24%,而未患有双相障碍的婴儿死亡率为3.7),神经发育障碍发生率更高。结论:胎龄> 31周的婴儿BD是一个额外的生存和神经发育风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Bronchopulmonary dysplasia. Course over 3 years in 88 children born between 1984 and 1988].

Background: The survival and outcome of infants with bronchopulmonary dysplasia (BD) depend on the patient's maturity, the severity of the BD and nutritional problems. This study evaluates the specific role of chronic pulmonary failure in the growth and development of infants recovering from BD.

Population and methods: 88 infants admitted for BD from January 1984 to December 1988, having gestational age from 25 to 41 weeks 5 days (mean: 29) and birth weight from 680 to 3,400 g (mean: 1,195) were studied. All infants were given respiratory support for 6 to 914 days (mean 84) and oxygen therapy for 28 to 1,232 days (mean: 119). 29 infants were given corticosteroids for more than 1 month. The outcome of the 80 infants with gestational ages of less than 33 weeks was compared to that of 272 infants with the same gestational age but not suffering from BD on their 28th day. The infants in both groups were examined at 2 years of age and classified as: a) handicapped (neurologic deficit, IQ < 80, hearing loss, blindness, convulsions); b) doubtful (transitory neurology dysfunction); c) normal.

Results: Of the 88 infants still living at the age of 28 days, 19 died before the age of 2 years: 16 of the 64 surviving infants who could be followed until the age of 2 years were classified as handicapped, 13 were considered doubtful and 35 were normal. The more significant risk factors for neurodevelopmental impairment were: a) the presence of porencephaly and/or ventricular dilatation on brain ultrasonography; b) head circumference < -2 SD at the end of hospital stay; c) oxygen therapy and hospitalization > 5-6 months. The group of infants with BD had a higher death rate (24% vs. 3.7 in the group without BD) and more frequent neurodevelopmental impairment at gestational ages of > 31-32 weeks.

Conclusions: BD is an extra risk for the survival and neurodevelopment of infants with gestational age > 31 weeks.

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