Mitha Ayoub, Chen Ruoqing, Razaz Neda, Johansson Stefan, Stephansson Olof, Altman Maria, Bolk Jenny
Division of Clinical Epidemiology, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
CHU Lille, Pediatric and Neonatal Intensive Care Transport Unit, Department of Emergency Medicine, Lille, France.
BMJ. 2024 Jan 24;384:e075630. doi: 10.1136/bmj-2023-075630.
To assess long term neurodevelopmental outcomes of children born at different gestational ages, particularly 32-33 weeks (moderately preterm) and 34-36 weeks (late preterm), compared with 39-40 weeks (full term).
Nationwide cohort study.
Sweden.
1 281 690 liveborn singleton children without congenital malformations born at 32 to 41 weeks between 1998 and 2012.
The primary outcomes of interest were motor, cognitive, epileptic, hearing, and visual impairments and a composite of any neurodevelopmental impairment, diagnosed up to age 16 years. Hazard ratios and 95% confidence intervals were estimated using Cox regression adjusted for parental and infant characteristics in the study population and in the subset of full siblings. Risk differences were also estimated to assess the absolute risk of neurodevelopmental impairment.
During a median follow-up of 13.1 years (interquartile range 9.5-15.9 years), 75 311 (47.8 per 10 000 person years) liveborn singleton infants without congenital malformations had at least one diagnosis of any neurodevelopmental impairment: 5899 (3.6 per 10 000 person years) had motor impairment, 27 371 (17.0 per 10 000 person years) cognitive impairment, 11 870 (7.3 per 10 000 person years) epileptic impairment, 19 700 (12.2 per 10 000 person years) visual impairment, and 20 393 (12.6 per 10 000 person years) hearing impairment. Children born moderately or late preterm, compared with those born full term, showed higher risks for any impairment (hazard ratio 1.73 (95% confidence interval 1.60 to 1.87) and 1.30 (1.26 to 1.35); risk difference 4.75% (95% confidence interval 3.88% to 5.60%) and 2.03% (1.75% to 2.35%), respectively) as well as motor, cognitive, epileptic, visual, and hearing impairments. Risks for neurodevelopmental impairments appeared highest from 32 weeks (the earliest gestational age), gradually declined until 41 weeks, and were also higher at 37-38 weeks (early term) compared with 39-40 weeks. In the sibling comparison analysis (n=349 108), most associations remained stable except for gestational age and epileptic and hearing impairments, where no association was observed; for children born early term the risk was only higher for cognitive impairment compared with those born full term.
The findings of this study suggest that children born moderately or late preterm have higher risks of adverse neurodevelopmental outcomes. The risks should not be underestimated as these children comprise the largest proportion of children born preterm. The findings may help professionals and families achieve a better risk assessment and follow-up.
评估不同孕周出生儿童的长期神经发育结局,特别是与孕39 - 40周(足月)相比,孕32 - 33周(中度早产)和孕34 - 36周(晚期早产)出生儿童的情况。
全国队列研究。
瑞典。
1998年至2012年间在32至41周出生的1,281,690例无先天性畸形的单胎活产儿童。
主要关注的结局是运动、认知、癫痫、听力和视力障碍以及任何神经发育障碍的综合情况,诊断时间截至16岁。使用Cox回归估计风险比和95%置信区间,并根据研究人群及全同胞子集中的父母和婴儿特征进行调整。还估计了风险差异以评估神经发育障碍的绝对风险。
在中位随访13.1年(四分位间距9.5 - 15.9年)期间,75,311例(每10,000人年47.8例)无先天性畸形的单胎活产婴儿至少有一次任何神经发育障碍的诊断:5899例(每10,000人年3.6例)有运动障碍,27,371例(每10,000人年17.0例)有认知障碍,11,870例(每10,000人年7.3例)有癫痫障碍,19,700例(每10,000人年12.2例)有视力障碍,20,393例(每10,000人年12.6例)有听力障碍。与足月出生的儿童相比,中度或晚期早产出生的儿童出现任何障碍(风险比1.73(95%置信区间1.60至1.87)和1.30(1.2б至1.35);风险差异分别为4.75%(95%置信区间3.88%至5.60%)和2.03%(1.75%至2.35%))以及运动、认知、癫痫、视力和听力障碍的风险更高。神经发育障碍的风险从32周(最早孕周)开始似乎最高,逐渐下降直至41周,并且与孕з9 - 40周相比,孕37 - 38周(早期足月)时也更高。在同胞比较分析(n = 349,108)中,除孕周以及癫痫和听力障碍外,大多数关联保持稳定,其中未观察到关联;对于早期足月出生的儿童,与足月出生的儿童相比,仅认知障碍风险更高。
本研究结果表明,中度或晚期早产出生的儿童出现不良神经发育结局的风险更高。这些风险不应被低估,因为这些儿童占早产出生儿童的最大比例。这些发现可能有助于专业人员和家庭进行更好的风险评估和随访。