European experience of steroid therapy in children with developmental and epileptic encephalopathy with spike wave activation in sleep ((D)EE-SWAS).

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Dilan Canbay, Floor E Jansen, Jan Schönberger, Victoria San Antonio-Arce, Julia Jacobs, Kerstin Alexandra Klotz
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引用次数: 0

Abstract

Background: Developmental and epileptic encephalopathy with spike wave activation in sleep (DEE-SWAS) and epileptic encephalopathy with spike wave activation in sleep (EE-SWAS) are rare but well-known childhood epileptic disorders. Steroids are one of the first line treatment options, but a variety of steroid regimens exists. The aim of this survey was to evaluate the practices of steroid therapy in the treatment of (D)EE-SWAS across European centers.

Methods: An online survey was conducted (via 'SurveyMonkey' Europe) among European epilepsy centers. Questions asked included: characteristics of replying center, applied definition of DEE-SWAS, existence of regional/national guidelines regarding diagnostic and therapeutic management. Particular attention was paid to the indication/contraindication of steroids and treatment regimens used.

Results: Responses were obtained from 60 centers across 18 countries. Only 15% of centers reported the availability of national guidelines for the management of (D)EE-SWAS. There were variations in definition of (D)EE-SWAS, with Spike-Wave- Index (SWI) > 85 (irrespective of cognitive status) and SWI > 50% with concurrent neurodevelopmental regression being the most prevalent, reported in 36% and 50%, respectively. Steroids and clobazam were considered the predominant treatment options, with the primary indication for steroids being neurodevelopmental arrest (52%) and failure of clobazam treatment (51%). Treatment goals of steroid treatment primarily focused on neurodevelopmental improvement (95%), and reduction of SWI (66%). Methylprednisolone and prednisone were the most frequently used steroids, although other steroid types were also reported. Pulse therapy was utilized exclusively in 47% of centers. The most commonly used steroid regimen was intravenous/oral methylprednisolone pulse therapy (20 mg/kg/day for 3 days, either monthly or weekly), although a broad variety of different regimens were reported. Criteria influencing decisions about steroid treatment were largely based on personal experience, with scientific publications playing a role in decision-making in only 14% of centers.

Conclusion: Steroids are part of the first line therapy of (D)EE-SWAS across Europe, but heterogeneity in formulations, dosages, and regimens persists due to limited guideline availability. The absence of comparative studies and the discordant definitions of (D)EE-SWAS further hinder comparisons of treatment efficacy. We recommend that harmonizing steroid treatment strategies is imperative for optimizing (D)EE-SWAS management.

欧洲类固醇治疗发育性和癫痫性脑病伴睡眠尖峰波激活的经验((D)EE-SWAS)。
背景:发育性和癫痫性脑病伴睡眠尖波激活(DEE-SWAS)和癫痫性脑病伴睡眠尖波激活(EE-SWAS)是罕见但众所周知的儿童癫痫疾病。类固醇是一线治疗选择之一,但存在多种类固醇治疗方案。本调查的目的是评估类固醇治疗在欧洲各中心治疗(D)EE-SWAS的实践。方法:在欧洲癫痫中心进行在线调查(通过“SurveyMonkey”Europe)。询问的问题包括:答复中心的特点、DEE-SWAS的应用定义、是否存在关于诊断和治疗管理的区域/国家指南。特别注意类固醇的适应症/禁忌症和使用的治疗方案。结果:从18个国家的60个中心获得了反馈。只有15%的中心报告了国家(D)EE-SWAS管理指南的可用性。(D)EE-SWAS的定义存在差异,Spike-Wave- Index (SWI) bbb85(与认知状态无关)和SWI > 50%,其中并发神经发育倒退最为普遍,分别为36%和50%。类固醇和氯巴唑被认为是主要的治疗选择,类固醇的主要适应症是神经发育停止(52%)和氯巴唑治疗失败(51%)。类固醇治疗的治疗目标主要集中在神经发育改善(95%)和减少SWI(66%)。甲基强的松龙和强的松是最常用的类固醇,尽管其他类型的类固醇也有报道。47%的中心只使用脉冲疗法。最常用的类固醇治疗方案是静脉注射/口服甲基强的松龙脉冲治疗(20mg /kg/天,3天,每月或每周),尽管有各种不同的治疗方案报道。影响类固醇治疗决策的标准主要基于个人经验,只有14%的中心在决策中发挥了科学出版物的作用。结论:类固醇是整个欧洲(D)EE-SWAS一线治疗的一部分,但由于指南可用性有限,配方、剂量和方案仍然存在异质性。比较研究的缺乏和(D)EE-SWAS定义的不一致进一步阻碍了治疗效果的比较。我们建议协调类固醇治疗策略是优化(D)EE-SWAS管理的必要条件。
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
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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