斯奇潘托预防和终止癫痫状态的有效性和安全性:系统综述。

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY
Epilepsia Open Pub Date : 2024-10-03 DOI:10.1002/epi4.13036
Nicola Specchio, Stéphane Auvin, Adam Strzelczyk, Francesco Brigo, Vicente Villanueva, Eugen Trinka
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引用次数: 0

摘要

癫痫状态(SE)是一种危及生命的急症,发病率和死亡率都很高。对于癫痫患者来说,SE 的治疗重点在于早期药物治疗。斯替潘托是一种第三代抗癫痫药物(ASM),已被批准用于治疗德雷维综合征的难治性全身强直-阵挛发作。本系统综述的目的是评估斯奇潘托在降低德雷维综合征或任何以复发性 SE 为特征的癫痫患者 SE 发生率方面的有效性和安全性。我们对 PubMed 和 Cochrane 数据库进行了系统检索,并对灰色文献进行了手工检索。根据标题和摘要对检索结果进行筛选;纳入了有关斯奇潘托对 SE 结果(包括 SE 停止、SE 发作次数减少或住院次数减少)影响的研究数据。在确定的 66 条记录中,有 17 项研究符合纳入条件,其中 15 项为人类研究(n = 474;年龄 1.1-78 岁),2 项为动物实验。回顾性或前瞻性观察研究的结果表明,在氯巴扎铵或丙戊酸钠等 ASMs 的基础上加用司立潘妥,可降低德雷维综合征或其他发育性和癫痫性脑病(DEEs)患者 SE 的发病率。平均68%的患者(41%-100%)的SE发作次数比基线减少了≥50%,26%-100%的患者(平均77%)在开始使用司立潘妥后不再出现SE。此外,该综述还发现,作为急性治疗使用的斯利潘托也可有效阻止超难治性SE,但数据仅限于三个回顾性病例系列。施替潘托的耐受性普遍良好。总之,斯替潘托可降低德雷维综合征患者和其他可能患有德雷维综合征的患者的SE发作率,并可促进有癫痫发作史和无癫痫发作史的患者停止超级难治性SE。白话摘要:癫痫状态(SE)是一种危及生命、持续时间较长的癫痫发作,多发于癫痫患者/无癫痫患者。本文分析了 15 项已发表的研究,这些研究调查了抗癫痫药物斯奇潘托对预防癫痫患者癫痫发作(预防)或停止癫痫发作(停止)的效果和安全性,以及两项调查斯奇潘托如何发挥作用的动物实验。在癫痫患者中,41%-100%的患者使用斯奇潘托后SE发作次数减少了一半,26%-100%的患者不再发作SE,并且认为斯奇潘托具有良好的耐受性。对于患有/不患有癫痫的患者,在麻醉剂等其他药物不起作用后,斯奇潘托可能会阻止癫痫发作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficacy and safety of stiripentol in the prevention and cessation of status epilepticus: A systematic review

Efficacy and safety of stiripentol in the prevention and cessation of status epilepticus: A systematic review

Status epilepticus (SE) is a life-threatening emergency with high morbidity and mortality. In people with epilepsy, the management of SE is focused on early medical treatment. Stiripentol is a third-generation antiseizure medication (ASM) approved for refractory generalized tonic–clonic seizures in Dravet syndrome. The aim of this systematic review was to evaluate the effectiveness and safety of stiripentol in reducing the incidence of SE in patients with Dravet syndrome or any epilepsy characterized by recurrent SE. The PubMed and Cochrane databases were systematically searched, and gray literature was hand-searched. Search results were screened by title and abstract; studies with data on the effect of stiripentol on SE outcomes, including the cessation of SE, reduction in number of SE episodes, or reduction in hospitalizations, were included. Of 66 records identified, 17 studies were eligible for inclusion, of which 15 were human studies (n = 474; aged 1.1–78 years), and two were animal experiments. Results of retrospective or prospective observational studies showed that stiripentol as add-on therapy to ASMs such as clobazam or valproate reduced the incidence of SE in patients with Dravet syndrome or other developmental and epileptic encephalopathies (DEEs). A mean of 68% of patients (range 41%–100%) had a ≥50% reduction in SE episodes from baseline, and 26%–100% of patients (mean 77%) became SE-free after stiripentol initiation. Moreover, this review found stiripentol, used as acute treatment, may also be effective for the cessation of super-refractory SE, but data are limited to three retrospective case series. Stiripentol was generally well-tolerated. In conclusion, stiripentol reduces the incidence of SE episodes in patients with Dravet syndrome and potentially other DEEs, and it promotes cessation of super-refractory SE in patients with and without a history of seizures.

Plain Language Summary

Status epilepticus (SE) is a life-threatening, long-lasting seizure occurring in patients with/without epilepsy. This article analyzed 15 published studies that investigated the effects and safety of the anti-seizure medication stiripentol for preventing SE in epilepsy patients (prevention) or stopping an SE episode (cessation), and two animal studies that investigated how stiripentol works. In epilepsy patients, stiripentol halved the number of SE episodes in 41–100% of patients, 26–100% of patients became SE-free, and stiripentol was considered to be well tolerated. In patients with/without epilepsy, stiripentol may stop the SE episode after other drugs like anesthetics have not worked.

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来源期刊
Epilepsia Open
Epilepsia Open Medicine-Neurology (clinical)
CiteScore
4.40
自引率
6.70%
发文量
104
审稿时长
8 weeks
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