The Efficacy of Lacosamide in Children with Drug-Resistant Epilepsy: Three Cases in Pediatric Patients

Q4 Medicine
Ji-Hoon Na, Hoon-Chul Kang, H. Kim
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引用次数: 0

Abstract

Lacosamide is a relatively new anti-seizure medication (ASM) that is classified as a sodium channel blocker (SCB). Unlike conventional SCBs, such as carbamazepine, phenytoin, and oxcarbazepine, lacosamide stabilizes hyperexcitable neuronal membranes by selectively enhancing the slow inactivation of voltage-gated sodium channels [1-3]. In addition, it exhibits relatively little interaction with other ASMs and has high utility because it has both oral and intravenous (IV) formulations. In recent years, IV lacosamide has increasingly been recognized as a useful treatment for status epilepticus [4,5]. Lacosamide has shown efficacy and safety not only in adults, but also in children [2]. As such, lacosamide has been approved for use as monotherapy and adjunctive therapy for the treatment of focal-onset seizures in adults, adolescents, and children aged ≥ 4 years with epilepsy in the European Union and the United States [3,6-8]. However, further research on the efficacy and safety of lacosamide in children is still needed. In particular, in South Korea, lacosamide has not yet been approved for use in patients with epilepsy among children under 16 years of age. Here, we report three cases of pediatric intractable focal epilepsy that were effectively treated with lacosamide add-on therapy. This study was approved by the Institutional Review Board of the Gangnam Severance Hospital, Yonsei University College of Medicine for the study of ASMs, including lacosamide, in refractory childhood epilepsy (3-2022-0135). The review board waived the need for informed consent for this retrospective study. Case 1: A 10-year-old girl with normal development without a specific birth history had intractable focal seizures at 24 months of age. After the seizures, she began experiencing cognitive decline. She took several ASMs, but they had no significant effect on seizure control, and her condition progressed to intractable epilepsy. In the pre-surgical evaluation, brain magnetic resonance imaging (MRI) was normal; however, focality was found in the right frontal area on fluorodeoxyglucose-positron emission tomography (PET) and electroencephalography (EEG) (Fig. 1A). Hence, she qualified for epilepsy surgery on her right frontal lobe. Her full-scale intelligence quotient (FSIQ) at that time was 69 and she weighed 31 kg. While awaiting epilepsy surgery, she was administered lacosamide as an add-on therapy. She became seizure-free after the titration of lacosamide up to 200 mg/day. Her seizures stopped for more than a year after the treatment, with no
拉沙酰胺治疗儿童耐药性癫痫的疗效观察——附3例儿科患者
拉科沙胺是一种相对较新的抗癫痫药物(ASM),被归类为钠通道阻滞剂(SCB)。与卡马西平、苯妥英和奥卡西平等传统scb不同,拉科沙胺通过选择性地增强电压门控钠通道的缓慢失活来稳定高兴奋性神经元膜[1-3]。此外,它表现出相对较少的相互作用与其他asm和具有很高的效用,因为它有口服和静脉注射(IV)制剂。近年来,静脉注射拉科沙胺越来越被认为是治疗癫痫持续状态的有效方法[4,5]。拉科沙胺不仅在成人中,而且在儿童中也显示出有效性和安全性。因此,在欧盟和美国,拉科沙胺已被批准作为单一疗法和辅助疗法,用于治疗成人、青少年和≥4岁癫痫儿童的局灶性癫痫发作[3,6-8]。然而,拉科沙胺在儿童中的有效性和安全性仍需进一步研究。特别是在韩国,拉科沙胺尚未被批准用于16岁以下儿童癫痫患者。在这里,我们报告了三例小儿顽固性局灶性癫痫的有效治疗与拉科沙胺附加治疗。该研究获得延世大学医学院江南Severance医院机构审查委员会批准,用于研究包括拉科沙胺在内的抗痉挛药在难治性儿童癫痫中的应用(3-2022-0135)。审查委员会放弃了对这项回顾性研究知情同意的需要。病例1:一名发育正常,无特殊出生史的10岁女孩在24月龄时出现难治性局灶性癫痫。癫痫发作后,她的认知能力开始下降。她服用了几次抗痉挛药物,但对控制癫痫发作没有明显效果,病情发展为顽固性癫痫。术前评估,脑磁共振成像(MRI)正常;然而,氟脱氧葡萄糖正电子发射断层扫描(PET)和脑电图(EEG)在右侧额叶区域发现了病灶(图1A)。因此,她有资格接受右额叶癫痫手术。当时她的全面智商(FSIQ)为69,体重为31公斤。在等待癫痫手术期间,她被给予拉科沙胺作为附加治疗。拉科沙胺滴定至200mg /d后,患者无癫痫发作。治疗后,她的癫痫发作停止了一年多,没有任何症状
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来源期刊
Annals of Child Neurology
Annals of Child Neurology Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.50
自引率
0.00%
发文量
35
审稿时长
8 weeks
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