Luna D, Dulac O, Pajot N, Beaumont D
Service de Neuro-Pédiatrie, U29 INSERM, Hopital St. Vincent de Paul, Paris, France.
Epilepsia. 1989 Jul-Aug;30(4):430-7. doi: 10.1111/j.1528-1157.1989.tb05322.x.
Sixty-one pediatric patients (12-229 months of age) with refractory epilepsy were treated with vigabatrin [gamma-vinyl GABA (GVG)] in a 16-week, single-blind, add-on, placebo-controlled trial. Twenty-three patients (38%) showed a reduction of more than 50% in seizure frequency; 12 patients (20%) experienced a seizure increase; and the remaining 26 did not show significant differences between placebo and GVG treatment. Among the 216 patients who entered the long-term phase after having experienced more than 50% decrease in seizure frequency, 14 continued with the same degree of improvement after 2-11 months of follow-up (mean 7.7). GVG was particularly efficient in cryptogenic partial epilepsy. Conversely, nonprogressive myoclonic epilepsy tended to be aggravated. Agitation was the most commonly observed side effect, mainly at onset of therapy in mentally retarded patients, but was easily reversed by dose reduction. GVG is a promising drug in the treatment of refractory epilepsies of childhood.
在一项为期16周的单盲、附加、安慰剂对照试验中,61例难治性癫痫患儿(年龄12 - 229个月)接受了氨己烯酸[γ-乙烯基氨基丁酸(GVG)]治疗。23例患者(38%)癫痫发作频率降低超过50%;12例患者(20%)癫痫发作增加;其余26例患者在安慰剂和GVG治疗之间未显示出显著差异。在癫痫发作频率降低超过50%后进入长期阶段的216例患者中,14例在随访2 - 11个月(平均7.7个月)后保持相同程度的改善。GVG在隐源性部分性癫痫中特别有效。相反,非进行性肌阵挛癫痫往往会加重。激惹是最常见的副作用,主要在治疗开始时出现在智力发育迟缓的患者中,但通过减少剂量很容易逆转。GVG是治疗儿童难治性癫痫的一种有前景的药物。