Department of Pediatrics, Neonatal-Perinatal Medicine, University of Texas Medical School at Houston, Houston, TX, USA.
J Pediatr. 2013 Apr;162(4):685-690.e1. doi: 10.1016/j.jpeds.2012.09.054. Epub 2012 Nov 8.
To test the hypothesis that high-risk ventilator-dependent extremely low birth weight (birth weight ≤1000 g) infants treated with 7 days of hydrocortisone will have larger total brain tissue volumes than placebo treated infants.
A predetermined sample size of 64 extremely low birth weight infants, between 10-21 days old and ventilator-dependent with a respiratory index score ≥2, were randomized to systemic hydrocortisone (17 mg/kg cumulative dose) or saline placebo. Primary outcome was total brain tissue volume. Volumetric magnetic resonance imaging was performed at 38 weeks postmenstrual age; brain tissue regions were segmented and quantified automatically with a high degree of accuracy and 9 structures were segmented manually. All analyses of regional brain volumes were adjusted by postmenstrual age at magnetic resonance imaging scan.
The study groups were similar at baseline and 8 infants died in each arm. Unadjusted total brain tissue volume (mean ± SD) in the hydrocortisone (N = 23) and placebo treated infants (N = 21) was 272 ± 40.3 cm(3) and 277.8 ± 59.1 cm(3), respectively (adjusted mean difference: 6.35 cm(3) (95% CI: (-20.8, 32.5); P = .64). Three of the 31 hydrocortisone treated infants and 5 of the 33 placebo treated infants survived without severe bronchopulmonary dysplasia (relative risk 0.62, 95% CI: 0.13, 2.66; P = .49). No significant differences were noted in prespecified secondary outcomes of regional structural volumes or days on respiratory support. No adverse effects of hydrocortisone were observed.
Low dose hydrocortisone in high-risk ventilator-dependent infants after a week of age had no discernible effect on regional brain volumes or pulmonary outcomes prior to neonatal intensive care unit discharge.
验证假设,即接受 7 天氢化可的松治疗的高危呼吸机依赖极低出生体重(出生体重≤1000g)婴儿的总脑组织体积大于安慰剂治疗的婴儿。
在 10-21 天龄且呼吸指数评分≥2 的呼吸机依赖极低出生体重婴儿中,预先确定了 64 名婴儿的样本量,随机分为全身氢化可的松(17mg/kg 累积剂量)或生理盐水安慰剂组。主要结局为总脑组织体积。在出生后 38 周进行磁共振成像;使用高度精确的自动方法对组织体积进行磁共振成像扫描;手动分割 9 个结构。对所有区域性脑体积的分析均通过磁共振成像扫描时的校正后的胎龄进行调整。
研究组在基线时相似,每组有 8 名婴儿死亡。接受氢化可的松(N=23)和安慰剂治疗(N=21)的婴儿的未调整总脑组织体积(平均值±标准差)分别为 272±40.3cm3和 277.8±59.1cm3(调整后的平均差异:6.35cm3(95%置信区间:(-20.8,32.5);P=0.64)。31 名接受氢化可的松治疗的婴儿中有 3 名和 33 名接受安慰剂治疗的婴儿中没有出现严重的支气管肺发育不良(相对风险 0.62,95%置信区间:0.13,2.66;P=0.49)。未观察到指定的次要结局(区域性结构体积或呼吸支持天数)有显著差异。没有观察到氢化可的松的不良反应。
一周龄后高危呼吸机依赖的婴儿接受低剂量氢化可的松治疗,在新生儿重症监护病房出院前对区域性脑体积或肺部结局没有明显影响。