Al-Twajri Waleed A, Shevell Michael I
Department of Neurology/Neurosurgery, McGill University, Montreal Children's Hospital-McGill University Health Centre, Montreal, Quebec.
J Child Neurol. 2002 Dec;17(12):901-4.
The objective of this study was to compare the clinical and electroencephalographic features of two groups of children with benign epilepsy of childhood with rolandic spikes: those in whom seizure control was attained either without the use of medication or with a single medication (group 1) and those requiring two medications for seizure control (group 2). A consecutive series of children with benign epilepsy of childhood with rolandic spikes was identified in a single pediatric neurology practice. Medical charts were then systematically retrospectively reviewed. A total of 66 children with benign epilepsy of childhood with rolandic spikes was identified; 52 (78.8%) required either no medication (n = 7) or a single medication (n = 45) for seizure control, whereas 14 (21.2%) required two medications. The two groups did not differ with respect to gender, age of onset, type (generalized or partial) of initial seizure, or whether EEG abnormalities were unilateral or bilateral. They did differ significantly with respect to the mean number of seizures experienced prior to initiating treatment (group 1, 2.06, versus group 2, 4.36; t = 3.40, P = .005). In those treated (n = 59), the initial medication selected (carbamazepine versus noncarbamazepine) in the two groups was significantly different: group 1, 40 (carbamazepine)/45, versus group 2, 9 (carbamazepine)/14; chi2 = 4.59; P = .03. The difference in frequency between the two groups of associated comorbid conditions (tics, attention-deficit hyperactivity disorder [ADHD], learning disability) almost reached the threshold of statistical significance: group 1, 7/52, versus group 2, 5/14 (chi2 = 3.67, P = .06). A subset of children with benign epilepsy of childhood with rolandic spikes may require more than one medication for effective seizure control. This subset experiences more seizures prior to the initiation of treatment, is more likely to be treated initially with a noncarbamazepine medication, and tends to have a higher frequency of associated conditions.
一组患者在未使用药物或仅使用单一药物的情况下实现了癫痫发作控制(第1组),另一组患者需要两种药物才能控制癫痫发作(第2组)。在一家儿科神经科诊所中,连续纳入了一系列伴有中央颞区棘波的儿童良性癫痫患者。然后对病历进行了系统的回顾性审查。共确定了66例伴有中央颞区棘波的儿童良性癫痫患者;52例(78.8%)在癫痫发作控制时无需用药(7例)或仅使用单一药物(45例),而14例(21.2%)需要两种药物。两组在性别、发病年龄、首发癫痫发作类型(全身性或部分性)或脑电图异常是单侧还是双侧方面没有差异。但在开始治疗前经历的癫痫发作平均次数方面存在显著差异(第1组为2.06次,第2组为4.36次;t = 3.40,P = .005)。在接受治疗的患者(59例)中,两组最初选择的药物(卡马西平与非卡马西平)有显著差异:第1组,40例(卡马西平)/45例,第2组,9例(卡马西平)/14例;χ2 = 4.59;P = .03。两组相关合并症(抽动症、注意力缺陷多动障碍[ADHD]、学习障碍)的发生频率差异几乎达到统计学意义阈值:第1组,7/52例,第2组,5/14例(χ2 = 3.67,P = .06)。一部分伴有中央颞区棘波的儿童良性癫痫患者可能需要不止一种药物才能有效控制癫痫发作。这部分患者在开始治疗前癫痫发作次数更多,更有可能最初使用非卡马西平药物治疗,并且合并症的发生频率往往更高。