重组人红细胞生成素给药对早产儿严重脑室内出血的影响:单中心经验

Ha Na Lee, Jeong Min Lee, S. H. Kim, S. Park, Jiyoon Jeong, Euiseok Jung, B. Lee
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引用次数: 0

摘要

目的:研究产后早期给予促红细胞生成素(EPO)对重度脑室内出血(IVH)早产儿神经发育结局和发病率的影响。方法:回顾性分析孕龄23+0周至31+6周的诊断为重度IVH并接受EPO治疗至少2周的早产儿的医疗记录。我们比较了两组患者的临床特征、主要并发症和神经发育障碍。主要结果是矫正年龄18至26个月时严重的神经发育障碍。重度神经发育障碍定义为贝利婴儿发育量表II智力发育指数或精神运动发育指数<70或诊断为脑瘫。结果:研究纳入33例早产儿(平均胎龄25.2±1.6周,平均出生体重775.1±224.5 g), EPO按400或1000 IU/kg剂量给予,每周3次,从出生后10.7±6.9天开始,平均维持58.6±25.9天。我们观察到EPO组(n=14)和对照组(n=19)的围产期特征无差异。同样,EPO组(85.7%)和对照组(78.9%)的严重神经发育障碍率也没有差异。新生儿发病率包括支气管肺发育不良、坏死性小肠结肠炎和早产儿视网膜病变在EPO组和对照组之间也相似。结论:早期应用EPO并不能降低重度IVH早产儿发生严重神经发育障碍的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Recombinant Human Erythropoietin Administration in Premature Infants with Severe Intraventricular Hemorrhage: A Single-Center Experience
Purpose: We investigated the effects of early postnatal administration of erythropoietin (EPO) on neurodevelopmental outcomes and morbidities in preterm infants with severe grades of intraventricular hemorrhage (IVH).Methods: We retrospectively reviewed the medical records of preterm infants of gestational age 23+0 weeks to 31+6 weeks, who were diagnosed with severe grades of IVH and received EPO over at least 2 weeks. We compared clinical characteristics, major complications, and neurodevelopmental impairment between the two groups. The primary outcome was severe neurodevelopmental impairment at 18 to 26 months of corrected age. Severe neurodevelopmental impairment was defined as a mental developmental index or psychomotor developmental index of <70 on the Bayley Scales of Infant Development II or diagnosis of cerebral palsy.Results: The study included 33 preterm infants (mean gestational age 25.2±1.6 weeks and mean birth weight 775.1±224.5 g). EPO was administered at a dose of 400 or 1,000 IU/kg thrice weekly and was maintained over a mean period of 58.6± 25.9 days beginning from 10.7±6.9 days after birth. We observed no difference in perinatal characteristics between the EPO (n=14) and the control group (n=19). Similarly, severe neurodevelopmental impairment rates did not differ between the EPO (85.7%) and control groups (78.9%). The incidence of neonatal morbidities including bronchopulmonary dysplasia, necrotizing enterocolitis, and retinopathy of prematurity was also similar between the EPO and control groups.Conclusion: Early administration of EPO did not reduce the risk of severe neurodevelopmental impairment in preterm infants with severe IVH.
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