Sharawat Indar Kumar, Panda Prateek Kumar, Kumar Vinod, Sherwani Poonam
Pediatric Neurology Division, Department of Pediatrics, All India Institute of Medical Sciences, Rishikesh 249203, India.
Department of Pediatrics, All India Institute of Medical Sciences, Rishikesh 249203, India.
J Trop Pediatr. 2022 Apr 5;68(3). doi: 10.1093/tropej/fmac032.
In newly diagnosed neurocysticercosis (NCC) with seizures, the choice of anti-seizure medication (ASM) seems to be arbitrary due to a lack of comparative studies. Although oxcarbazepine (OXC) is often considered efficacious for focal seizures in NCC, due to adverse effects, newer ASMs like levetiracetam (LCM) and lacosamide are also being explored.
This study was performed by case record review of children with newly diagnosed solitary viable parenchymal NCC aged 4-18years who received lacosamide and OXC at least for 12 weeks between August 2019 and April 2021, from a prospective registry of a tertiary care teaching hospital in north India. Seizure control, electroencephalographic abnormalities, resolution of inflammatory granulomas and adverse effects were compared between two arms at 12 and 24 weeks.
Total 31 (8.3 ± 4.7 years, 19 boys) and 72 (8.6 ± 4.2 years, 43 boys) completed at least 12 weeks follow-up in LCM and OXC groups, out of which 2 and 51 completed at least 24 weeks follow-up in LCM and OXC groups, respectively. The occurrence of breakthrough seizure was comparable in both arms at 12 and 24 weeks (1/31 and 2/22 in lacosamide group vs. 2/72 and 4/51 in OXC group, p = 0.66 and 0.59, respectively). Patients receiving OXC had more frequent treatment-emergent adverse events (p = 0.0001) and four patients required discontinuation due to severe adverse events (SAEs), while none in the lacosamide group had SAEs.
Lacosamide appears to be efficacious and safe for achieving seizure freedom in patients with solitary viable parenchymal neurocysticercosis.
在新诊断的伴有癫痫发作的神经囊尾蚴病(NCC)中,由于缺乏对比研究,抗癫痫药物(ASM)的选择似乎具有随意性。尽管奥卡西平(OXC)通常被认为对NCC中的局灶性癫痫发作有效,但由于不良反应,也在探索左乙拉西坦(LCM)和拉科酰胺等新型ASM。
本研究通过对2019年8月至2021年4月期间在印度北部一家三级护理教学医院的前瞻性登记处登记的4至18岁新诊断为孤立性存活实质性NCC且接受拉科酰胺和奥卡西平至少12周的儿童进行病例记录回顾。在12周和24周时比较两组的癫痫控制情况、脑电图异常、炎性肉芽肿的消退情况和不良反应。
LCM组和OXC组分别有31例(8.3±4.7岁,19名男孩)和72例(8.6±4.2岁,43名男孩)完成了至少12周的随访,其中LCM组和OXC组分别有2例和51例完成了至少24周的随访。在12周和24周时,两组突破性癫痫发作的发生率相当(拉科酰胺组为1/31和2/22,奥卡西平组为2/72和4/51,p分别为0.66和0.59)。接受奥卡西平治疗的患者出现治疗中出现的不良事件更频繁(p = 0.0001),有4例患者因严重不良事件(SAE)需要停药,而拉科酰胺组无一例出现SAE。
拉科酰胺对于孤立性存活实质性神经囊尾蚴病患者实现无癫痫发作似乎有效且安全。