Fois A, Buoni S, Di Bartolo R M, Di Marco V, Mostardini R
Institute of Clinical Pediatrics, University of Siena, Italy.
Childs Nerv Syst. 1994 May;10(4):244-8. doi: 10.1007/BF00301162.
Sixty-nine children, aged from 2 months to 16 years and suffering from different types of drug-resistant epileptic seizures, mostly complex partial and secondary generalised, were recruited in an open, uncontrolled, prospective study of treatment with vigabatrin (gamma-vinyl GABA). Following a 3-month baseline observation period, the initial dose of vigabatrin of 10 mg/kg per day was progressively increased up to a maximum of 140 mg/kg per day, in addition to the conventional concomitant therapy. Sixteen patients showed a > or = 50% reduction in seizure frequency compared with the baseline, with complete control of seizures in nine cases. In 14 other patients, no substantial change in seizure frequency was observed, although an improvement in psychological performance after vigabatrin treatment warranted further continuation of the drug. In 35 patients vigabatrin was discontinued because of lack of efficacy (22 cases) and/or increased seizure frequency (13 cases). The clinical and biological tolerance of vigabatrin was remarkably good.
69名年龄在2个月至16岁之间、患有不同类型耐药性癫痫发作(主要是复杂部分性发作和继发性全身性发作)的儿童被纳入一项关于氨己烯酸(γ-乙烯基γ-氨基丁酸)治疗的开放性、非对照前瞻性研究。在为期3个月的基线观察期之后,除常规联合治疗外,氨己烯酸的初始剂量为每日10mg/kg,并逐渐增加至最大每日140mg/kg。与基线相比,16名患者的癫痫发作频率降低了≥50%,其中9例癫痫发作得到完全控制。在另外14名患者中,虽然氨己烯酸治疗后心理表现有所改善,因此有必要继续用药,但癫痫发作频率未观察到实质性变化。35名患者因缺乏疗效(22例)和/或癫痫发作频率增加(13例)而停用氨己烯酸。氨己烯酸的临床和生物学耐受性非常好。