食道闭锁患者患自闭症谱系障碍和智力残疾的风险增加,但注意力缺陷/多动障碍的风险没有增加。

Ann-Marie Kassa, Cecilia Arana Håkanson, Helene Engstrand Lilja
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摘要

关于食道闭锁(EA)患者的神经发育障碍,如注意缺陷/多动障碍(ADHD)、自闭症谱系障碍(ASD)和智力残疾(ID)的知识很少。本研究的目的是调查EA患者ADHD、ASD和ID的患病率和风险。数据来自瑞典四个纵向人群登记中心,并使用Cox比例风险回归进行分析。1973-2018年在瑞典出生的EA患者与每个个体的5个对照组一起纳入,暴露与性别、出生胎龄、出生年份和出生县相匹配。排除有染色体畸变和综合征的个体。总共包括735名EA患者和3675名对照者。研究时的中位年龄为20岁(3-48岁)。EA患者中有24例(3.9%)出现ASD, 34例(5.5%)出现ADHD, 28例(4.6%)出现ID。与对照组相比,EA患者出现ASD的风险高1.66倍(95%置信区间[CI], 1.05-2.64),出现ID的风险高3.62倍(95% CI, 2.23-5.89)。ADHD的风险没有明显增加。有88.2%的EA和ADHD患者以及84.5%的ADHD对照患者接受了ADHD药物治疗。有EA的人患ASD和ID的风险比没有接触过EA的人高。这些结果对于建立EA儿童的随访计划非常重要,以便及时发现并因此获得早期治疗和支持,特别是在开学前。
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The risk of autism spectrum disorder and intellectual disability but not attention deficit/hyperactivity disorder is increased in individuals with esophageal atresia.

Knowledge of neurodevelopmental disorders such as attention deficit/hyperactivity disorder (ADHD), autism spectrum disorders (ASD) and intellectual disability (ID) in patients with esophageal atresia (EA) is scarce. The aims of this study were to investigate the prevalence and risk of ADHD, ASD and ID in individuals with EA. Data were obtained from four longitudinal population-based registries in Sweden and analyzed using Cox proportional hazards regression. Patients with EA born in Sweden in 1973-2018 were included together with five controls for each individual with the exposure matched on sex, gestational age at birth, birth year and birth county. Individuals with chromosomal aberrations and syndromes were excluded. In total, 735 individuals with EA and 3675 controls were included. Median age at time of the study was 20 years (3-48). ASD was found in 24 (3.9%), ADHD in 34 (5.5%) and ID in 28 (4.6%) individuals with EA. Patients with EA had a 1.66 times higher risk of ASD (95% confidence interval [CI], 1.05-2.64) and a 3.62 times higher risk of ID (95% CI, 2.23-5.89) compared with controls. The risk of ADHD was not significantly increased. ADHD medication had been prescribed to 88.2% of patients with EA and ADHD and to 84.5% of controls with ADHD. Individuals with EA have a higher risk of ASD and ID than individuals without the exposure. These results are important when establishing follow-up programs for children with EA to allow timely detection and consequentially an earlier treatment and support especially before school start.

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