Arican Pinar, Gencpinar Pinar, Olgac Dundar Nihal, Tekgul Hasan
Department of Pediatric Neurology, Kahramanmaraş Necip Fazil Hospital, Kahramanmaraş, Turkey.
Department of Pediatric Neurology, Izmir Katip Celebi University, Izmir, Turkey.
J Pediatr Neurosci. 2021 Apr-Jun;16(2):91-96. doi: 10.4103/jpn.JPN_137_20. Epub 2021 Jul 2.
Electrical status epilepticus during slow-wave sleep (ESES) is an epilepsy syndrome with sleep-induced epileptic discharges and acquired impairment of cognition or behavior. Since the disease's original description in 1971, no clear consensus has emerged on diagnostic criteria or optimal treatment. The treatment of ESES can be challenging, often including numerous antiepileptic drugs, immunomodulatory agents, and even surgical interventions. There is little evidence to guide treatment because only retrospective studies and case reports on the efficacy of treatment of ESES are present in literature. In this paper, we aim to analyze the etiopathogenesis of ESES in the new genetic era and to evaluate the treatment modalities in accordance with the genetic data and electroclinic spectrum of ESES.
慢波睡眠期癫痫性电持续状态(ESES)是一种伴有睡眠诱发癫痫放电以及获得性认知或行为损害的癫痫综合征。自1971年首次描述该疾病以来,关于其诊断标准或最佳治疗方法尚未形成明确的共识。ESES的治疗颇具挑战性,通常涉及多种抗癫痫药物、免疫调节剂,甚至手术干预。由于文献中仅有关于ESES治疗效果的回顾性研究和病例报告,几乎没有证据可指导治疗。在本文中,我们旨在分析新基因时代ESES的病因发病机制,并根据ESES的基因数据和电临床谱评估其治疗方式。