Panda Prateek Kumar, Sharawat Indar Kumar, Dawman Lesa, Panda Pragnya, Kasinathan Ananthanarayanan, Rathaur Vyas Kumar
Division of Pediatric Neurology, Department of Pediatrics, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
Department of Pediatrics, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
J Neurosci Rural Pract. 2022 Jan 7;13(1):32-42. doi: 10.1055/s-0041-1740580. eCollection 2022 Jan.
Lennox-Gastaut syndrome (LGS) is one of the most difficult to treat childhood-onset epileptic encephalopathies. There is growing evidence that lacosamide is safe and efficacious in patients and adults with refractory epilepsy. However, the evidence regarding the efficacy of lacosamide in LGS is controversial so far. We aimed to evaluate the efficacy and tolerability of lacosamide in patients with LGS. We conducted a systematic review on MEDLINE, EMBASE, COCHRANE CENTRAL, Google Scholar, and Web of Science, collating all available literature till July 31, 2020. The qualitative review included case reports, case series, and both controlled/uncontrolled trials as well as retrospective studies, but for determining pooled estimates, we only included studies with a sample size of 5 or more. The primary outcome was the efficacy of lacosamide in patients with LGS. Clinical variables related to efficacy and adverse events attributed to lacosamide were extracted from each publication. The pooled estimate of variables related to these parameters was performed using a random-effect model. Of the 68 items identified by the search, 14 were reviewed as full-text. Eleven articles including two prospective and six retrospective studies fulfilled eligibility criteria and described outcomes in 81 patients (42 adults, 39 children, 60% male, range-1.4-61 years). On average, 35.2%, 27.9%, 7.3%, and 29.4% patients had > 50% reduction, < 50% reduction, no change, and worsening of seizure frequency, respectively. Although 36% of patients had adverse events like somnolence, behavioral abnormalities including irritability, aggressiveness, nausea, tremor, memory problems, dizziness, gastrointestinal discomfort, vomiting, and weight loss, no serious adverse events were noted. The evidence available in the current literature is not sufficient to support or refute the use of lacosamide in patients with LGS. Although it is one of the possible therapeutic options worth exploring in patients with LGS, caution is still necessary, as there are reports of worsening of seizure frequency in some patients.
伦诺克斯 - 加斯托综合征(LGS)是最难治疗的儿童期起病的癫痫性脑病之一。越来越多的证据表明,拉科酰胺对难治性癫痫患者和成人是安全有效的。然而,迄今为止,关于拉科酰胺在LGS中的疗效证据存在争议。我们旨在评估拉科酰胺对LGS患者的疗效和耐受性。
我们对MEDLINE、EMBASE、Cochrane Central、谷歌学术和科学网进行了系统综述,整理了截至2020年7月31日的所有可用文献。定性综述包括病例报告、病例系列以及对照/非对照试验和回顾性研究,但为了确定合并估计值,我们仅纳入样本量为5或更多的研究。主要结局是拉科酰胺对LGS患者的疗效。从每个出版物中提取与疗效相关的临床变量以及归因于拉科酰胺的不良事件。使用随机效应模型对与这些参数相关的变量进行合并估计。
在检索到的68篇文献中,14篇作为全文进行了综述。11篇文章(包括2篇前瞻性研究和6篇回顾性研究)符合纳入标准,描述了81例患者(42例成人,39例儿童,60%为男性,年龄范围1.4 - 61岁)的结局。平均而言,分别有35.2%、27.9%、7.3%和29.4%的患者癫痫发作频率降低超过50%、降低不足50%、无变化以及恶化。虽然36%的患者出现了嗜睡、包括易怒、攻击性在内的行为异常、恶心、震颤、记忆问题、头晕、胃肠道不适、呕吐和体重减轻等不良事件,但未观察到严重不良事件。
当前文献中的证据不足以支持或反驳拉科酰胺在LGS患者中的使用。虽然它是LGS患者值得探索的可能治疗选择之一,但仍需谨慎,因为有报道称一些患者的癫痫发作频率会恶化。