Division of Neonatology, Beatrix Children's Hospital, University Medical Center, University of Groningen, Groningen, Netherlands.
Pediatrics. 2012 Aug;130(2):e265-72. doi: 10.1542/peds.2012-0079. Epub 2012 Jul 9.
Children born moderately preterm (32-35(6/7) weeks' gestation) are at increased risk of both neonatal morbidities and developmental delays in early childhood. It is unknown whether neonatal morbidities contribute to the increased risk of developmental delay. The objective of this study was to determine the effect of neonatal morbidities after moderately preterm birth on development at preschool age.
In a community-based, stratified cohort, parents of 832 moderately preterm children born in 2002 or 2003 completed the Ages and Stage Questionnaire when their child was 43 to 49 months old. Data on Apgar scores, asphyxia, tertiary NICU admission, hospital transfer, circulatory insufficiency, hypoglycemia, septicemia, mechanical ventilation, continuous positive airway pressure, apneas, caffeine treatment, and hyperbilirubinemia were obtained from medical records. We assessed associations of neonatal characteristics with developmental delay, adjusted for gender, small-for-gestational-age status, gestational age, and maternal education.
Hypoglycemia and asphyxia were associated with developmental delay; odds ratios (ORs) were 2.42 (95% confidence interval [CI]: 1.23-4.77) and 3.18 (95% CI: 1.01-10.0), respectively. Tertiary NICU admission and hyperbilirubinemia had positive but statistically borderline nonsignificant associations with developmental delay: ORs were 1.74 (95% CI: 0.96-3.15) and 1.52 (95% CI: 0.94-2.46), respectively. No other neonatal morbidities were associated with developmental delay. In multivariate analyses, only hypoglycemia was associated with developmental delay (OR: 2.19; 95% CI: 1.08-4.46).
In moderately preterm-born children, only hypoglycemia increased the risk of developmental delay at preschool age. A concerted effort to prevent hypoglycemia might enhance developmental outcome in this group.
出生时为中度早产儿(32-35(6/7) 孕周)的儿童存在新生儿期多种并发症和儿童早期发育迟缓的风险增加。目前尚不清楚新生儿期多种并发症是否会增加发育迟缓的风险。本研究的目的是确定中度早产儿出生后新生儿期多种并发症对学龄前儿童发育的影响。
在一项基于社区的分层队列研究中,2002 年或 2003 年出生的 832 名中度早产儿的父母在其孩子 43-49 个月时完成了《年龄与阶段问卷》。从病历中获取了新生儿的 Apgar 评分、窒息、三级新生儿重症监护病房(NICU)入院、医院转院、循环功能不全、低血糖、败血症、机械通气、持续气道正压通气、呼吸暂停、咖啡因治疗和高胆红素血症等数据。我们评估了新生儿特征与发育迟缓之间的关联,同时调整了性别、小于胎龄儿状态、胎龄和母亲教育等因素。
低血糖和窒息与发育迟缓相关;比值比(ORs)分别为 2.42(95%置信区间[CI]:1.23-4.77)和 3.18(95% CI:1.01-10.0)。三级 NICU 入院和高胆红素血症与发育迟缓呈正相关,但统计学上有显著意义(ORs 分别为 1.74(95% CI:0.96-3.15)和 1.52(95% CI:0.94-2.46))。其他新生儿期多种并发症与发育迟缓无关。在多变量分析中,只有低血糖与发育迟缓相关(OR:2.19;95% CI:1.08-4.46)。
在中度早产儿中,只有低血糖会增加学龄前儿童发育迟缓的风险。协同努力预防低血糖可能会改善该人群的发育结局。