14 Comorbidities Affecting Children with Autism Spectrum Disorder: A Retrospective Chart Review from the Main Referral Site for ASD Evaluation in Manitoba

IF 1.8 4区 医学 Q2 PEDIATRICS
Jessy Burns, Ryan Phung, Shayna McNeill, Ana Hanlon-Dearman, M Florencia Ricci
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Abstract

Abstract Background Autism Spectrum Disorder (ASD) is a developmental disorder characterized by deficits in social interaction/communication, restricted interests and repetitive behaviours. Recent discussions have emerged worldwide regarding a possible “overly-inclusive” diagnosis of ASD, adding heterogeneity around presentation/etiology and comorbidities. Objectives This study aimed to determine the frequency and characteristics of comorbidities among children diagnosed with ASD in Manitoba, and to evaluate differences in presentation between those with and without medical comorbidities. As comorbid neurodevelopmental disorders such as global developmental delay (GDD) and attention-deficit yyperactivity disorder (ADHD) are common in children with ASD, these were not included as “medical comorbidities” and were studied separately. Design/Methods We conducted a retrospective chart review of >2000 electronic charts at the main referral site for children <6 years requiring evaluation for ASD in Manitoba. All children aged 0-5 years diagnosed with ASD at this site between May 2016 to September 2021 were identified. X2 and t test were used to compare groups. Results Of the total of 1858 children identified, 1459 (78%) were male, 252 (13.5%) were born prematurely, 504 (27%) had ≥1 medical comorbidity. Most common medical comorbidities were neurological (12.7%) and allergies/eczema (6.1%). Comorbid GDD was diagnosed in 428 (23%). Age of referral to RCC and age of diagnosis did not differ between groups. Medical comorbidities were more common among preterm children (31% vs. 26%, p:<0.01) and children with comorbid GDD (35% vs. 18.6%, p:<0.01). There was no significant difference in overall presence of medical comorbidities by sex (29.5% vs. 26.6%, p: 0.25); however, girls had a statistically significant higher incidence of neurological comorbidities, e.g. cerebral palsy, epilepsy, hypotonia NYD (16% vs. 12%, p:0.03). Conclusion Results of this study are consistent with previous studies, which note high comorbidity rates among children with ASD. The high rates of associated neurological conditions, GDD, and prematurity add heterogeneity to this group and may relate to the reported “overly-inclusive” diagnosis. This study will be used as a catalyst for guiding further prospective studies in the area.
14种影响自闭症谱系障碍儿童的合并症:来自马尼托巴省ASD评估主要转诊站点的回顾性图表综述
自闭症谱系障碍(Autism Spectrum Disorder, ASD)是一种以社会交往/沟通缺陷、兴趣限制和重复性行为为特征的发育障碍。最近在世界范围内出现了关于ASD诊断可能“过度包容”的讨论,增加了表现/病因和合并症的异质性。目的本研究旨在确定曼尼托巴省诊断为ASD的儿童共病的频率和特征,并评估有和没有医学共病的儿童在表现上的差异。由于整体发育迟缓(GDD)和注意力缺陷多动障碍(ADHD)等共病性神经发育障碍在ASD儿童中很常见,因此这些未被纳入“医学共病”,并被单独研究。设计/方法我们对马尼托巴省6岁以下需要评估ASD的儿童主要转诊点的2000张电子图表进行了回顾性分析。所有在2016年5月至2021年9月期间被诊断为ASD的0-5岁儿童均被确定。组间比较采用X2检验和t检验。结果1858例患儿中,男性1459例(78%),早产252例(13.5%),合并症504例(27%)。最常见的医学合并症是神经系统(12.7%)和过敏/湿疹(6.1%)。428人(23%)被诊断为共病性GDD。转介到RCC的年龄和诊断年龄在两组之间没有差异。医疗合并症在早产儿(31%比26%,p:<0.01)和患有GDD合并症的儿童(35%比18.6%,p:<0.01)中更为常见。医学合并症的总体存在性在性别上没有显著差异(29.5% vs 26.6%, p: 0.25);然而,女孩的神经系统合并症发生率有统计学上的显著性增高,如脑瘫、癫痫、低张力NYD(16%比12%,p:0.03)。结论本研究结果与先前的研究一致,即ASD患儿的合并症发生率较高。相关神经系统疾病、GDD和早产的高发生率增加了该组的异质性,并可能与报道的“过度包容”诊断有关。本研究将作为指导该领域进一步前瞻性研究的催化剂。
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来源期刊
Paediatrics & child health
Paediatrics & child health 医学-小儿科
CiteScore
2.10
自引率
5.30%
发文量
208
审稿时长
>12 weeks
期刊介绍: Paediatrics & Child Health (PCH) is the official journal of the Canadian Paediatric Society, and the only peer-reviewed paediatric journal in Canada. Its mission is to advocate for the health and well-being of all Canadian children and youth and to educate child and youth health professionals across the country. PCH reaches 8,000 paediatricians, family physicians and other child and youth health professionals, as well as ministers and officials in various levels of government who are involved with child and youth health policy in Canada.
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