Al Ajlouni S, Shorman A, Daoud A S
Department of Pediatrics, King Hussain Medical Center, Amman, Jordan.
Seizure. 2005 Oct;14(7):459-63. doi: 10.1016/j.seizure.2005.07.009. Epub 2005 Aug 8.
This study has been conducted to assess the efficacy and safety of topiramate in refractory epilepsies in infants and young children.
A prospective clinical trial was performed in three tertiary care hospitals, on 47 children aged 6-60 months with refractory epilepsy. Topiramate was added to at least two baseline anti-epileptic drugs. The efficacy was rated according to seizure type, frequency and duration.
Children with refractory epilepsy were classified according to their clinical, neuro-imaging, and neurophysiological profile into infantile spasms (IS) (9 cases, 19%), Lennox-Gastaut syndrome (LGS) (25 cases, 53%) and other epilepsies (13 cases, 28%). Children were also classified into cryptogenic and symptomatic epilepsy. Topiramate was introduced as add-on therapy in a daily dose of 1 mg/kg/day for 2 weeks, followed by increments of 1-3 mg/kg/day at 2-week intervals, up to a maximum of 10 mg/kg/day. After a minimum treatment period of 6 months, 28 (60%) of the children had a satisfactory response (completely seizure free, or more than a 50% seizure reduction). The remaining 19 children (40%) had an unsatisfactory response (50% or less reduction in seizure frequency, no change or increased seizure frequency). Topiramate appeared to be equally effective in infantile spasms, Lennox-Gastaut syndrome and children with other types of epilepsy, with no significant difference between those with a satisfactory and an unsatisfactory response (p=0.089). There was also no significant difference in response between patients with cryptogenic and symptomatic epilepsy (p=0.360). Mild to moderate adverse effects, mainly somnolence, anorexia and nervousness, were present in 25 (53%) of children. One of the children developed hypothyroidism.
Although the long term safety and possible adverse effects of topiramate have not been fully established in infants and young children, this study has shown that it is a useful option for children with frequent seizures unresponsive to standard anti-epileptic drugs.
本研究旨在评估托吡酯治疗婴幼儿难治性癫痫的疗效和安全性。
在三家三级医疗机构对47例6至60个月的难治性癫痫患儿进行了一项前瞻性临床试验。托吡酯被添加到至少两种基线抗癫痫药物中。根据癫痫发作类型、频率和持续时间对疗效进行评估。
难治性癫痫患儿根据其临床、神经影像学和神经生理学特征分为婴儿痉挛症(IS)(9例,19%)、 Lennox-Gastaut综合征(LGS)(25例,53%)和其他癫痫(13例,28%)。患儿还被分为隐源性癫痫和症状性癫痫。托吡酯作为添加疗法引入,初始日剂量为1mg/kg/天,持续2周,随后每2周增加1 - 3mg/kg/天,最大剂量为10mg/kg/天。经过至少6个月的治疗期后,28例(60%)患儿有满意的反应(完全无癫痫发作,或癫痫发作减少超过50%)。其余19例患儿(40%)反应不满意(癫痫发作频率减少50%或更少、无变化或癫痫发作频率增加)。托吡酯在婴儿痉挛症、Lennox-Gastaut综合征和其他类型癫痫患儿中似乎同样有效,满意反应组和不满意反应组之间无显著差异(p = 0.089)。隐源性癫痫和症状性癫痫患者之间的反应也无显著差异(p = 0.360)。25例(53%)患儿出现轻度至中度不良反应,主要为嗜睡、厌食和紧张。其中1例患儿出现甲状腺功能减退。
尽管托吡酯在婴幼儿中的长期安全性和可能的不良反应尚未完全明确,但本研究表明,对于对标准抗癫痫药物无反应的频繁发作患儿,托吡酯是一种有用的选择。