Neßler Jasmin, Rundfeldt Chris, Löscher Wolfgang, Kostic Draginja, Keefe Thomas, Tipold Andrea
Department of Small Animal Medicine and Surgery, University of Veterinary Medicine, 30559, Hannover, Germany.
Department of Pharmacology, Toxicology and Pharmacy, University of Veterinary Medicine Hannover, 30559, Hannover, Germany.
BMC Vet Res. 2017 Jan 25;13(1):33. doi: 10.1186/s12917-017-0957-z.
Imepitoin was tested as a combination treatment with phenobarbital in an open-label mono-centre cohort study in dogs with drug-resistant epilepsy. Diagnosis of idiopathic epilepsy was based on clinical findings, magnetic resonance imaging and cerebrospinal fluid analysis. Three cohorts were treated. In cohort A, dogs not responding to phenobarbital with or without established add-on treatment of potassium bromide or levetiracetam were treated add-on with imepitoin, starting at 10 mg/kg BID, with titration allowed to 30 mg/kg BID. In cohort B, the only difference to cohort A was that the starting dose of imepitoin was reduced to 5 mg/kg BID. In cohort C, animals not responding to imepitoin at >20 mg/kg BID were treated with phenobarbital add-on starting at 0.5 mg/kg BID.
The add-on treatment resulted in a reduction in monthly seizure frequency (MSF) in all three cohorts. A reduction of ≥50% was obtained in 36-42% of all animals, without significant difference between cohorts. The lower starting dose of 5 mg/kg BID imepitoin was better tolerated, and an up-titration to on average of 15 mg/kg BID was sufficient in cohort A and B. In cohort C, a mean add-on dose of 1.5 mg/kg BID phenobarbital was sufficient to achieve a clinically meaningful effect. Six dogs developed a clinically meaningful increase in MSF of ≥ 50%, mostly in cohort A. Neither imepitoin nor phenobarbital add-on treatment was capable of suppressing cluster seizure activity, making cluster seizure activity an important predictor for drug-resistance.
A combination treatment of imepitoin and phenobarbital is a useful treatment option for a subpopulation of dogs with drug-resistant epilepsy, a low starting dose with 5 mg/kg BID is recommended.
在一项针对耐药性癫痫犬的开放标签单中心队列研究中,对艾美苯妥英与苯巴比妥联合治疗进行了测试。特发性癫痫的诊断基于临床症状、磁共振成像和脑脊液分析。共治疗了三个队列。在队列A中,对苯巴比妥无反应(无论是否已确立添加溴化钾或左乙拉西坦治疗)的犬只接受艾美苯妥英添加治疗,起始剂量为10mg/kg,每日两次,允许滴定至30mg/kg,每日两次。在队列B中,与队列A的唯一区别是艾美苯妥英的起始剂量降至5mg/kg,每日两次。在队列C中,对艾美苯妥英剂量>20mg/kg,每日两次无反应的动物,接受苯巴比妥添加治疗,起始剂量为0.5mg/kg,每日两次。
添加治疗使所有三个队列的每月癫痫发作频率(MSF)均降低。所有动物中有36%-42%的癫痫发作频率降低≥50%,各队列之间无显著差异。艾美苯妥英5mg/kg,每日两次的较低起始剂量耐受性更好,在队列A和B中,平均滴定至15mg/kg,每日两次就足够了。在队列C中,苯巴比妥平均添加剂量为1.5mg/kg,每日两次就足以产生临床意义上的效果。6只犬的MSF临床意义上增加≥50%,主要在队列A中。艾美苯妥英和苯巴比妥添加治疗均无法抑制丛集性癫痫发作活动,这使得丛集性癫痫发作活动成为耐药性的重要预测指标。
艾美苯妥英和苯巴比妥联合治疗是耐药性癫痫犬亚群的一种有效治疗选择,建议起始剂量为5mg/kg,每日两次。