Karadeniz Technical University Medical Faculty Department of Pediatric Neurology, Trabzon, Turkey.
Gazi University Medical Faculty Department of Pediatric Neurology, Ankara, Turkey.
Epilepsy Res. 2022 Aug;184:106963. doi: 10.1016/j.eplepsyres.2022.106963. Epub 2022 Jun 6.
To evaluate the effectiveness and tolerability of clobazam therapy in the pediatric population in terms of seizure semiology, epileptic syndromes, and etiological subgroups.
A retrospective cohort study was conducted consisting of 1710 epileptic children from eight centers in seven geographic regions of Turkey. The initial efficacy of clobazam therapy was evaluated after three months of treatment. The long-term effectiveness of the drug, overall seizure outcomes, and overall therapeutic outcomes were evaluated during 12 months of therapy.
Analysis of initial efficacy after the first three months of clobazam therapy showed that 320 (18.7 %) patients were seizure-free, 683 (39.9 %) had > 50 % seizure reductions, and 297 (17.4 %) had < 50 % seizure reductions. A positive response (seizure-free and >50 % seizure reduction) was determined for focal-onset (62.3 %) seizures, epileptic spasms (61.5 %), and generalized onset seisures (57.4). The highest positive response rate among the epileptıc syndromes was for self-limited epilepsy with centrotemporal spikes (SeLECTS). The highest negative response rate was for developmental and/or epileptic encephalopathies (DEEs). Magnetic resonance imaging (MRI) revealed a structural etiological diagnosis in 25.8 % of the cohort. A higher positive response rate was observed at MRI in patients with sequelae lesions than in those with congenital lesions. The seizure recurrence rate was higher in the patient group with epilepsy wıth genetic and metabolic causes, in individuals with more than one seizure type, and in those using three or more antiseizure drugs.
This cohort study provides additional evidence that clobazam is an effective and well-tolerable drug with a high seizure-free rate (18.7 %), a significant seizure reduction rate (57.3 %), and with excellent overall therapeutic outcomes with a low seizure relapse rate and considerable reversible benefits in the pediatric population.
评估氯巴占治疗小儿癫痫的疗效和耐受性,从发作表现、癫痫综合征和病因亚组方面进行评价。
本研究为回顾性队列研究,纳入土耳其七个地区的八个中心的 1710 例癫痫患儿。评估患儿在接受氯巴占治疗 3 个月后的初步疗效。在治疗 12 个月期间,评估药物的长期疗效、总体发作结局和总体治疗结局。
氯巴占治疗 3 个月后的初步疗效分析显示,320 例(18.7%)患儿无发作,683 例(39.9%)发作减少>50%,297 例(17.4%)发作减少<50%。局灶性发作(62.3%)、癫痫性痉挛(61.5%)和全面性发作(57.4%)的阳性反应(无发作和发作减少>50%)比例较高。在癫痫综合征中,具有自限性中央颞区棘波的良性癫痫(SeLECTS)的阳性反应率最高。发育性和/或癫痫性脑病(DEE)的阴性反应率最高。磁共振成像(MRI)显示该队列中有 25.8%的患儿存在结构性病因诊断。在有后遗症病变的患儿中,MRI 阳性反应率更高。在有遗传和代谢病因的癫痫患儿、有多种发作类型的患儿和使用三种或三种以上抗癫痫药物的患儿中,癫痫发作复发率更高。
本队列研究提供了更多证据表明,氯巴占是一种有效且耐受性良好的药物,在小儿癫痫中具有较高的无发作率(18.7%)、显著的发作减少率(57.3%)和良好的总体治疗结局,癫痫发作复发率低,且具有相当大的可逆益处。