First-Drug Efficacy and Drug-Resistant Epilepsy Rates in Children With New-Onset Epilepsies: A Multicenter Large Cohort Study.

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY
Pinar Gencpinar, Pinar Arican, Nihal Olgac Dündar, Betül Kilic, Esra Sarigecili, Cetin Okuyaz, Kursad Aydin, Hasan Tekgul
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Abstract

Objective: This study aimed to assess the first-drug efficacy rate in newly diagnosed children with epilepsies treated with antiseizure medications. Methods: This retrospective study was conducted on 1003 children (age range: 3-10 years, and the mean duration of follow-up: 22 ± 13 months) with newly diagnosed epilepsy. The following parameters were evaluated: first-drug efficacy rate, first-drug-failure rate, and drug resistance rate in the cohort. Results: The first-drug-failure rate was defined in 335/1003 (33%) of the patients, no seizure control in 315 (31%), and drug withdrawal in 20 (2%). There was no significant difference between the group with focal-onset seizures and the group with generalized onset seizures. The first-drug efficacy rate was 67% in children with focal-onset seizures and 66% in children with generalized-onset seizures. Adjunctive antiseizure medication therapy was initiated in 335 patients-dual therapy with 180 patients (18%) and polytherapy with 155 (15%). Drug-resistant epilepsy was defined as 15% in the follow-up period. Etiology-specific diagnoses of the cohort were structural (n = 165, 17%), genetic (n = 25, 3%), metabolic (n = 15%), immune-infectious (n = 17 (2%), and unknown (n = 781, 77%). With a comparison of the 2 most common etiology subgroups (structural versus unknown), a first-drug efficacy rate of 53% and a higher prevalence of drug-resistant epilepsy at 30% were observed in children with structural etiology. First-drug efficacy was statistically lower in children without well-defined epilepsy syndromes (65%) compared with the rate of those with well-defined epilepsy syndrome (79%). Conclusion: This study revealed a first-drug failure rate (33%) in the presented cohort with a drug-resistance epilepsy rate (15%).

新发癫痫儿童的首药疗效和耐药癫痫率:多中心大型队列研究。
研究目的本研究旨在评估使用抗癫痫药物治疗的新确诊癫痫患儿的首次用药有效率。研究方法这项回顾性研究针对 1003 名新确诊的癫痫患儿(年龄范围:3-10 岁,平均随访时间:22 ± 13 个月)。研究评估了以下参数:队列中的首次用药有效率、首次用药失败率和耐药率。结果如下335/1003(33%)例患者首次用药失败,315(31%)例患者癫痫发作未得到控制,20(2%)例患者停药。局灶性发作组与全身性发作组之间没有明显差异。局灶性癫痫发作患儿的首次用药有效率为 67%,全身性癫痫发作患儿的首次用药有效率为 66%。335名患者接受了辅助抗癫痫药物治疗--180名患者接受了双重治疗(18%),155名患者接受了多重治疗(15%)。在随访期间,15%的患者被定义为耐药性癫痫。组群的特定病因诊断为结构性(165 例,17%)、遗传性(25 例,3%)、代谢性(15%)、免疫感染性(17 例,2%)和未知(781 例,77%)。通过对两个最常见的病因亚组(结构性与未知性)进行比较,发现结构性病因儿童的首次用药有效率为 53%,耐药性癫痫的发生率较高,为 30%。据统计,无明确癫痫综合征的儿童首次用药有效率(65%)低于有明确癫痫综合征的儿童(79%)。结论:这项研究显示,在所提交的队列中,首次用药失败率(33%)和耐药癫痫率(15%)都很高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Child Neurology
Journal of Child Neurology 医学-临床神经学
CiteScore
4.20
自引率
5.30%
发文量
111
审稿时长
3-6 weeks
期刊介绍: The Journal of Child Neurology (JCN) embraces peer-reviewed clinical and investigative studies from a wide-variety of neuroscience disciplines. Focusing on the needs of neurologic patients from birth to age 18 years, JCN covers topics ranging from assessment of new and changing therapies and procedures; diagnosis, evaluation, and management of neurologic, neuropsychiatric, and neurodevelopmental disorders; and pathophysiology of central nervous system diseases.
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