Gross Steven J, Anbar Ran D, Mettelman Barbara B
State University of New York Upstate Medical University, Syracuse, New York, USA.
Pediatrics. 2005 Mar;115(3):681-7. doi: 10.1542/peds.2004-0956.
Postnatal dexamethasone treatment of ventilator-dependent preterm infants results in rapid improvement in lung function and reduction in chronic lung disease. However, limited data are available on long-term outcomes after such therapy. We studied growth, neurodevelopmental, and pulmonary outcomes at adolescence in children who had participated in a double-blind, placebo-controlled trial of dexamethasone beginning at 2 weeks of age for the prevention of chronic lung disease.
Thirty-six infants (birth weight < or =1250 g and gestational age < or =30 weeks) who were dependent on mechanical ventilation at 2 weeks of age received a 42-day course of dexamethasone, an 18-day course of dexamethasone, or saline placebo. Twenty-two children survived to 15 years (69% of the 42-day dexamethasone group, 67% of the 18-day dexamethasone group and 45% of the control group), and all were evaluated. Intact survival was defined as survival with normal neurologic examination, IQ >70, and receiving education in the regular classroom.
There were no differences among groups for growth or incidence of neurologic abnormalities. The mean IQ for the 42-day dexamethasone group was 85 +/- 10 compared with 60 +/- 20 for the 18-day dexamethasone group and 73 +/- 23 for the control group. All children in the 42-day dexamethasone group were receiving education in the regular classroom compared with only 50% of the 18-day dexamethasone group and 40% of the control group. As a result, intact survival was significantly greater for the 42-day dexamethasone group (69%) than for either the 18-day dexamethasone group (25%) or the control group (18%). Pulmonary function was significantly better for the 42-day dexamethasone group compared with the 18-day dexamethasone group (eg, forced expiratory volume in 1 second: 90 +/- 16 vs 71 +/- 15% predicted, respectively).
A 42-day course of dexamethasone therapy beginning at 2 weeks of age in preterm infants who are at high risk for severe chronic lung disease was associated with improved long-term neurodevelopmental outcome. Although additional research is needed to establish the optimal steroid preparation, dosage, and duration of therapy, these data support the view that moderately early (beginning at 1-2 weeks) corticosteroid treatment is advantageous for a select group of ventilator-dependent preterm infants.
对依赖呼吸机的早产儿进行产后地塞米松治疗可使肺功能迅速改善,并减少慢性肺病的发生。然而,关于此类治疗后的长期预后的数据有限。我们研究了参加一项双盲、安慰剂对照的地塞米松试验(从2周龄开始用于预防慢性肺病)的儿童在青春期的生长、神经发育和肺部预后情况。
36例2周龄时依赖机械通气的婴儿(出生体重≤1250g,胎龄≤30周)接受了42天疗程的地塞米松、18天疗程的地塞米松或生理盐水安慰剂治疗。22名儿童存活至15岁(42天疗程地塞米松组的69%,18天疗程地塞米松组的67%,对照组的45%),并对所有儿童进行了评估。完整存活定义为神经学检查正常、智商>70且在普通教室接受教育的存活情况。
各组在生长或神经学异常发生率方面无差异。42天疗程地塞米松组的平均智商为85±10,而18天疗程地塞米松组为60±20,对照组为73±23。42天疗程地塞米松组的所有儿童都在普通教室接受教育,而18天疗程地塞米松组只有50%,对照组只有40%。因此,42天疗程地塞米松组的完整存活率(69%)显著高于18天疗程地塞米松组(25%)或对照组(18%)。42天疗程地塞米松组的肺功能明显优于18天疗程地塞米松组(例如,第1秒用力呼气量:分别为预测值的90±16%和71±15%)。
对于有严重慢性肺病高风险的早产儿,从2周龄开始进行42天疗程的地塞米松治疗与改善长期神经发育预后相关。尽管需要进一步研究以确定最佳的类固醇制剂、剂量和治疗持续时间,但这些数据支持这样的观点,即适度早期(从1 - 2周开始)的皮质类固醇治疗对选定的依赖呼吸机的早产儿是有利的。