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一项针对依赖呼吸机的早产儿的两种地塞米松治疗方案的多中心试验。

A multicenter trial of two dexamethasone regimens in ventilator-dependent premature infants.

作者信息

Papile L A, Tyson J E, Stoll B J, Wright L L, Donovan E F, Bauer C R, Krause-Steinrauf H, Verter J, Korones S B, Lemons J A, Fanaroff A A, Stevenson D K

机构信息

University of New Mexico, Albuquerque, USA.

出版信息

N Engl J Med. 1998 Apr 16;338(16):1112-8. doi: 10.1056/NEJM199804163381604.

Abstract

BACKGROUND

Ventilator-dependent premature infants are often treated with dexamethasone. However, the optimal timing of therapy is unknown.

METHODS

We compared the benefits and hazards of initiating dexamethasone therapy at two weeks of age and at four weeks of age in 371 ventilator-dependent very-low-birth-weight infants (501 to 1500 g) who had respiratory index scores (mean airway pressure x the fraction of inspired oxygen) of 52.4 at two weeks of age. One hundred eighty-two infants received dexamethasone for two weeks followed by placebo for two weeks, and 189 infants received placebo for two weeks followed by either dexamethasone (those with a respiratory-index score of > or =2.4 on treatment day 14) or additional placebo for two weeks. Dexamethasone was given at a dose of 0.25 mg per kilogram of body weight twice daily intravenously or orally for five days, and the dose was then tapered.

RESULTS

The median time to ventilator independence was 36 days in the dexamethasone-placebo group and 37 days in the placebo-dexamethasone group. The incidences of chronic lung disease (defined as the need for oxygen supplementation at 36 weeks' postconceptional age) were 66 percent and 67 percent, respectively. Dexamethasone was associated with an increased incidence of nosocomial bacteremia (relative risk, 1.5; 95 percent confidence interval, 1.1 to 2.1) and hyperglycemia (relative risk, 1.9; 95 percent confidence interval, 1.2 to 3.0) in the dexamethasone-placebo group, elevated blood pressure (relative risk, 2.9; 95 percent confidence interval, 1.2 to 6.9) in the placebo-dexamethasone group, and diminished weight gain and head growth (P< 0.001) in both groups.

CONCLUSIONS

Treatment of ventilator-dependent premature infants with dexamethasone at two weeks of age is more hazardous and no more beneficial than treatment at four weeks of ages.

摘要

背景

依赖呼吸机的早产儿常接受地塞米松治疗。然而,最佳治疗时机尚不清楚。

方法

我们比较了371例依赖呼吸机的极低出生体重儿(501至1500克)在2周龄和4周龄开始使用地塞米松治疗的益处和风险,这些患儿在2周龄时呼吸指数评分(平均气道压×吸入氧分数)为52.4。182例婴儿接受地塞米松治疗2周,随后接受安慰剂治疗2周,189例婴儿接受安慰剂治疗2周,随后根据情况接受地塞米松(治疗第14天呼吸指数评分≥2.4者)或额外安慰剂治疗2周。地塞米松剂量为每日每公斤体重0.25毫克,静脉注射或口服,共5天,然后逐渐减量。

结果

地塞米松-安慰剂组脱机的中位时间为36天,安慰剂-地塞米松组为37天。慢性肺病(定义为孕龄36周时仍需吸氧)的发生率分别为66%和67%。地塞米松-安慰剂组中,地塞米松与医院获得性菌血症发生率增加(相对危险度,1.5;95%可信区间,1.1至2.1)和高血糖(相对危险度,1.9;95%可信区间,1.2至3.0)相关;安慰剂-地塞米松组中,地塞米松与血压升高(相对危险度,2.9;95%可信区间,1.2至6.9)相关;两组均出现体重增加和头围增长减少(P<0.001)。

结论

2周龄时用地塞米松治疗依赖呼吸机的早产儿比4周龄时治疗更具风险,且益处并不更多。

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