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两剂早期静脉注射地塞米松用于预防呼吸窘迫综合征婴儿的支气管肺发育不良。

Two doses of early intravenous dexamethasone for the prevention of bronchopulmonary dysplasia in babies with respiratory distress syndrome.

作者信息

Sanders R J, Cox C, Phelps D L, Sinkin R A

机构信息

Department of Pediatrics (Neonatology, Strong Children's Medical Center, Rochester, New York 14642.

出版信息

Pediatr Res. 1994 Jul;36(1 Pt 1):122-8. doi: 10.1203/00006450-199407001-00022.

DOI:10.1203/00006450-199407001-00022
PMID:7936832
Abstract

Bronchopulmonary dysplasia is an important complication of ventilation in babies for which treatment with steroids has been advocated. We report the results of a phase I study of early i.v. dexamethasone to prevent the development of bronchopulmonary dysplasia in a high-risk population of ventilated premature babies, < 30 wk gestation, with surfactant-treated respiratory distress syndrome. This study used a limited dexamethasone dosing regimen to minimize toxicity but used administration early in the course of acute lung disease to interrupt the injury cycle. Forty babies were enrolled; 19 were randomized to receive dexamethasone (0.5 mg/kg birth weight at 12-18 h of age and a second dose 12 h later) and 21 were randomized to receive placebo (i.v. saline). The dexamethasone group required less ventilatory support (mean airway, peak inspiratory and end expiratory pressures, and intermittent mandatory ventilation) and supplemental oxygen after study d 4 (all p < 0.05, repeated measures analysis of variance). Improved tidal volume in the dexamethasone group, as measured by pulmonary function testing of infants who remained intubated, was seen on study d 7 (p = 0.02, t test). The dexamethasone group required shorter hospitalizations (median of 95 d versus 106 d, p = 0.01) (proportional hazards regression). Survival in the dexamethasone group was 89% versus 67% in the placebo group (p = 0.08, chi 2 analysis). Survival without bronchopulmonary dysplasia, diagnosed at 36 wk corrected gestational age, was 68% in the dexamethasone group versus 43% in the placebo group (p = 0.14).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

支气管肺发育不良是婴儿通气的一种重要并发症,有人主张用类固醇进行治疗。我们报告了一项I期研究的结果,该研究针对孕周<30周、患有经表面活性剂治疗的呼吸窘迫综合征的高危通气早产儿群体,早期静脉注射地塞米松以预防支气管肺发育不良的发生。本研究采用有限的地塞米松给药方案以将毒性降至最低,但在急性肺病病程早期给药以中断损伤周期。40名婴儿入组;19名被随机分配接受地塞米松(出生体重0.5mg/kg,在出生后12 - 18小时给药,12小时后给予第二剂),21名被随机分配接受安慰剂(静脉注射生理盐水)。地塞米松组在研究第4天后需要的通气支持(平均气道压、吸气峰压和呼气末压以及间歇强制通气)和补充氧气较少(所有p<0.05,重复测量方差分析)。通过对仍插管婴儿进行肺功能测试发现,地塞米松组在研究第7天潮气量有所改善(p = 0.02,t检验)。地塞米松组住院时间较短(中位数为95天对106天,p = 0.01)(比例风险回归)。地塞米松组的生存率为89%,而安慰剂组为67%(p = 0.08,卡方分析)。在矫正胎龄36周时诊断为无支气管肺发育不良的生存率,地塞米松组为68%,而安慰剂组为43%(p = 0.14)。(摘要截短为250字)

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