Palmer Katharine J, McTavish Donna
Adis International Limited, 41 Centorian Drive, Private Bag 65901, Mairangi Bay, Auckland 10, New Zealand.
Drugs. 1993 Jun;45(6):1041-1065. doi: 10.2165/00003495-199345060-00008.
Felbamate is currently being developed as an antiepileptic agent. Although its mechanism of action has yet to be fully elucidated, felbamate appears to inhibit both the spread of seizures and increase seizure threshold in animal models. Data available in the clinical setting provide evidence that, at doses of up to 3600 mg/day as an adjunct to existing antiepileptic therapy or as monotherapy following substitution for other medications, the drug reduces the frequency of partial onset seizures in adult patients refractory to conventional antiepileptic treatments. Felbamate is also effective in the treatment of Lennox-Gastaut syndrome in children, a severe epilepsy which is usually refractory to antiepileptic agents. The effect of felbamate in the treatment of generalised tonic-clonic seizures in adults with partial onset seizures which are secondarily generalised is promising but requires clarification in large-scale trials. The most common adverse effects occurring during administration of felbamate are mild to moderate gastrointestinal (nausea, vomiting and anorexia) and central nervous system (headache, somnolence, diplopia, dizziness and insomnia) disturbances. Drug interactions with other antiepileptic agents may prove problematic in terms of adverse effects. Thus, at this stage of its development, the antiepileptic efficacy of felbamate in treatment-refractory patients with partial onset seizures and Lennox-Gastaut syndrome has been proven but efficacy in generalised tonic-clonic seizures requires further substantiation in large well controlled and well designed clinical trials. In addition, a more comprehensive base of comparative clinical trials data is necessary to further clarify issues of relative efficacy and tolerability compared with other antiepileptic agents. The clinical implications of the drug interactions associated with felbamate also require more detailed investigation. These data will be awaited with interest and when available will help to place felbamate in perspective in the management of epilepsy.
非氨酯目前正作为一种抗癫痫药物进行研发。尽管其作用机制尚未完全阐明,但在动物模型中,非氨酯似乎既能抑制癫痫发作的扩散,又能提高癫痫阈值。临床数据表明,作为现有抗癫痫治疗的辅助药物或替代其他药物后的单药治疗,每日剂量高达3600毫克时,该药物可降低对传统抗癫痫治疗无效的成年患者部分性发作的频率。非氨酯对儿童Lennox-Gastaut综合征(一种通常对抗癫痫药物难治的严重癫痫)的治疗也有效。非氨酯对继发全身性发作的部分性发作成年患者全身性强直-阵挛发作的治疗效果有前景,但需要大规模试验予以明确。服用非氨酯期间最常见的不良反应是轻度至中度的胃肠道(恶心、呕吐和厌食)及中枢神经系统(头痛、嗜睡、复视、头晕和失眠)紊乱。与其他抗癫痫药物的药物相互作用在不良反应方面可能存在问题。因此,在其研发的现阶段,非氨酯对部分性发作难治性患者及Lennox-Gastaut综合征的抗癫痫疗效已得到证实,但对全身性强直-阵挛发作的疗效需要在大型、严格对照且设计良好的临床试验中进一步证实。此外,需要更全面的比较临床试验数据基础,以进一步阐明与其他抗癫痫药物相比的相对疗效和耐受性问题。与非氨酯相关的药物相互作用的临床意义也需要更详细的研究。我们期待这些数据,如有可用数据将有助于正确看待非氨酯在癫痫治疗中的作用。