Associations Between Developmental Disorders, Early Seizure Onset, and Polytherapy in Childhood Epilepsy.

IF 0.6 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Kento Ohta, Tohru Okanishi, Yoshihiro Maegaki
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引用次数: 0

Abstract

Background: Epilepsy patients often exhibit symptoms of attention deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD). This study aimed to compare the clinical characteristics of epilepsy in patients comorbid with ADHD/ASD and those diagnosed with ADHD/ASD after epilepsy onset.

Methods: We retrospectively reviewed patients under 18 years of age with epilepsy who visited Tottori University Hospital's Child Neurology Department during 2013-2022. Eligible patients had at least 2 years of follow-up after epilepsy onset and were taking antiseizure medication (ASM). We excluded those with epileptic encephalopathy, abnormal perinatal history, imaging abnormalities, or intellectual disabilities. We compared clinical characteristics between epilepsy patients with and without ADHD/ASD.

Results: Data were collected from 28 patients with ADHD/ASD and 87 without. Patients with ADHD/ASD had an earlier seizure onset (6.6 ± 3.9 vs. 8.7 ± 4.1 years, P = 0.018) and were more likely to receive ASM polytherapy (39% vs. 16%, P = 0.010). Seizure outcomes did not differ between the two groups. Of the 28 patients with ADHD/ASD, 11 were diagnosed after epilepsy onset, and these patients were more likely to require multiple ASMs than those without ADHD/ASD (45% vs. 16%, P = 0.035).

Conclusion: Patients comorbid with ADHD/ASD tend to have earlier seizure onset and require more ASM, while those diagnosed with ADHD/ASD after epilepsy onset also often need polytherapy. These findings suggest that severe early epilepsy can lead to developmental disorders, though long-term seizure outcomes are not necessarily poor in these patients.

儿童癫痫的发育障碍、早期癫痫发作和综合治疗之间的关系。
背景:癫痫患者通常表现为注意缺陷/多动障碍(ADHD)和自闭症谱系障碍(ASD)的症状。本研究旨在比较癫痫发作后并发ADHD/ASD患者与诊断为ADHD/ASD患者癫痫的临床特征。方法:回顾性分析2013-2022年在鸟取县大学医院儿童神经内科就诊的18岁以下癫痫患者。符合条件的患者在癫痫发作后至少随访2年,并服用抗癫痫药物(ASM)。我们排除了癫痫性脑病、异常围产期史、影像学异常或智力残疾的患者。我们比较了伴有和不伴有ADHD/ASD的癫痫患者的临床特征。结果:收集了28例ADHD/ASD患者和87例非ADHD/ASD患者的数据。ADHD/ASD患者癫痫发作更早(6.6±3.9年vs 8.7±4.1年,P = 0.018),接受ASM综合治疗的可能性更大(39% vs. 16%, P = 0.010)。两组患者的癫痫发作结果没有差异。在28例ADHD/ASD患者中,有11例是在癫痫发作后诊断的,这些患者比没有ADHD/ASD的患者更有可能需要多次asm(45%比16%,P = 0.035)。结论:ADHD/ASD合并症患者癫痫发作更早,需要更多的ASM,而癫痫发作后诊断为ADHD/ASD的患者也往往需要多重治疗。这些发现表明,严重的早期癫痫可导致发育障碍,尽管这些患者的长期癫痫发作结果并不一定差。
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来源期刊
Yonago acta medica
Yonago acta medica MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
1.60
自引率
0.00%
发文量
36
审稿时长
>12 weeks
期刊介绍: Yonago Acta Medica (YAM) is an electronic journal specializing in medical sciences, published by Tottori University Medical Press, 86 Nishi-cho, Yonago 683-8503, Japan. The subject areas cover the following: molecular/cell biology; biochemistry; basic medicine; clinical medicine; veterinary medicine; clinical nutrition and food sciences; medical engineering; nursing sciences; laboratory medicine; clinical psychology; medical education. Basically, contributors are limited to members of Tottori University and Tottori University Hospital. Researchers outside the above-mentioned university community may also submit papers on the recommendation of a professor, an associate professor, or a junior associate professor at this university community. Articles are classified into four categories: review articles, original articles, patient reports, and short communications.
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