Department of Paediatrics, Hôpital Nord, Université de la Méditerranée, Chemin des Bourrellys, 13015 Marseille Cedex 20, France.
Eur J Obstet Gynecol Reprod Biol. 2010 May;150(1):13-8. doi: 10.1016/j.ejogrb.2010.01.001. Epub 2010 Jan 27.
To analyse the incidence of neurodevelopmental disorders at the age 6-10 years, in children born at less than 32 weeks of amenorrhea, and to identify the perinatal and neonatal factors associated with adverse neurodevelopmental outcomes at this age.
Longitudinal prospective trial in a French university and tertiary perinatal care centre. A total of 350 preterm singletons born in hospital at less than 32 weeks of amenorrhea between 1997 and 2001 were included. Children were invited for examination to screen for neurocognitive disorders between 4 and 8 years of age and re-contacted when they were between 6 and 10 years of age to evaluate school results. Three profiles of neurocognitive outcome were defined (normal, minor disorder, or major disorder) and correlated with maternal, antenatal, perinatal, and neonatal factors.
The survival rate of our cohort was 80.8% (283/350) and the proportion of survivors followed-up was 71.4% (202/283). There were 137 children (68%) with normal profiles, 29 (14%) with minor disorders, and 36 (18%) with major disorders. For those born at less than 28 weeks of amenorrhea, the survival rate was 62.7% (64/102) and the proportion of survivors followed-up was 78.1% (50/64). Among these children, 24 (48.0%) had normal outcomes, 8 (16.0%) suffered from minor disorders, and 18 (36.0%) had major disorders. The three principal independent risk factors for major or minor disorders at school age were gestational age less than 28 weeks of amenorrhea (adjusted odds ratio: 1.28 [95% confidence interval: 1.06-1.56]), chronic lung disease at birth (adjusted odds ratio: 2.92 [95% confidence interval: 1.15-7.42]), and an abnormal electroencephalogram before discharge (adjusted odds ratio: 2.61 [95% confidence interval: 1.10-6.18]). Moreover, abnormal brain ultrasonography was identified as an independent risk factor for occurrence of major disorders (adjusted odds ratio: 2.98 [95% confidence interval: 1.31-6.71]).
Very preterm infants remain at high risk for long-term neurodevelopmental disorders. Several neonatal factors, particularly chronic lung disease, seem to be important determinants of long-term outcome.
分析胎龄小于 32 周的早产儿在 6-10 岁时神经发育障碍的发生率,并确定与该年龄段神经发育不良结局相关的围产期和新生儿因素。
这是一项在法国大学和三级围产期保健中心进行的纵向前瞻性试验。共纳入 1997 年至 2001 年间在医院出生的胎龄小于 32 周的 350 名单胎早产儿。在 4 至 8 岁时,儿童被邀请进行神经认知障碍筛查,并在 6 至 10 岁时重新联系以评估学业成绩。定义了三种神经认知结果的特征(正常、轻度障碍或重度障碍),并与产妇、产前、围产期和新生儿因素相关。
本队列的存活率为 80.8%(283/350),随访的幸存者比例为 71.4%(202/283)。有 137 名儿童(68%)具有正常的认知特征,29 名(14%)有轻度障碍,36 名(18%)有重度障碍。对于胎龄小于 28 周的婴儿,存活率为 62.7%(64/102),随访的幸存者比例为 78.1%(50/64)。在这些儿童中,24 名(48.0%)有正常的结局,8 名(16.0%)有轻度障碍,18 名(36.0%)有重度障碍。学龄期有或无轻度障碍的三个主要独立危险因素为胎龄小于 28 周(调整优势比:1.28 [95%置信区间:1.06-1.56])、出生时慢性肺部疾病(调整优势比:2.92 [95%置信区间:1.15-7.42])和出院前脑电图异常(调整优势比:2.61 [95%置信区间:1.10-6.18])。此外,异常的脑超声检查被确定为发生重度障碍的独立危险因素(调整优势比:2.98 [95%置信区间:1.31-6.71])。
极早产儿长期神经发育障碍的风险仍然很高。一些新生儿因素,特别是慢性肺部疾病,似乎是长期结局的重要决定因素。