Bektaş Gonca, Tekin Uğur, Özkan Melis Ulak, Yıldız Edibe Pembegül, Çalışkan Mine, Özmen Meral, Aydınlı Nur
Department of Pediatric Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Department of Child and Adolescent Psychiatry, Ege University Faculty of Medicine, Izmir, Turkey.
Epilepsy Behav. 2017 Jul;72:39-42. doi: 10.1016/j.yebeh.2017.04.042. Epub 2017 May 30.
Levetiracetam, a widely used antiepileptic drug in children, has been associated with psychosocial and behavioral problems, which are also influenced by epilepsy variables, including duration or seizure frequency.
The objective of this study is to investigate the frequency and timing of treatment-emergent psychosocial and behavioral problems in children receiving levetiracetam, irrespective of seizure variables which are possible confounders.
A prospective, case-control study with a 3-month follow-up was conducted. Consecutive children aged 6 to 16years with new-onset partial seizures were included in case of starting treatment with either levetiracetam or valproic acid. Psychosocial and behavioral functioning were assessed using a set of standardized questionnaires including Strengths and Difficulties Questionnaire (SDQ) and Children's Depression Inventory (CDI) at baseline, 1 and 3-month follow-up. Patients' baseline scores were compared to healthy subjects. The difference in the follow-up SDQ and CDI scores was evaluated in patients receiving levetiracetam and valproic acid.
A total of 101 participants were analyzed; 32 patients in levetiracetam group, 19 patients in valproic acid group and 50 healthy controls. Baseline SDQ and CDI scores were not statistically different between patients and healthy subjects (p>0.05). No statistically significant difference was observed in CDI, total and subscale SDQ scores between patients receiving levetiracetam or valproic acid during the study period (p>0.05). A girl aged 15years receiving levetiracetam had a CDI score of 18 without suicidal ideation at baseline. She developed suicidal ideation and depression, which resolved after switching of levetiracetam to valproic acid, at the 1-month follow-up. No other psychiatric or behavioral side-effects were observed in other patients.
Psychosocial and behavioral side-effects of levetiracetam treatment are not frequent and they don't emerge in most of children at lower doses. At this dose, and after 3months, using these specific instruments, we did not observe any difference between the valproic acid and levetiracetam treatment groups.
左乙拉西坦是一种在儿童中广泛使用的抗癫痫药物,它与心理社会和行为问题有关,而这些问题也受到癫痫变量的影响,包括病程或发作频率。
本研究的目的是调查接受左乙拉西坦治疗的儿童中治疗引发的心理社会和行为问题的频率及发生时间,不考虑可能作为混杂因素的癫痫变量。
进行了一项为期3个月随访的前瞻性病例对照研究。年龄在6至16岁、新发部分性发作且开始使用左乙拉西坦或丙戊酸治疗的连续儿童被纳入研究。在基线、1个月和3个月随访时,使用一套标准化问卷,包括长处与困难问卷(SDQ)和儿童抑郁量表(CDI),对心理社会和行为功能进行评估。将患者的基线分数与健康受试者进行比较。对接受左乙拉西坦和丙戊酸治疗的患者随访时SDQ和CDI分数的差异进行评估。
共分析了101名参与者;左乙拉西坦组32例患者,并丙戊酸组19例患者和50名健康对照。患者与健康受试者之间的基线SDQ和CDI分数无统计学差异(p>0.05)。在研究期间,接受左乙拉西坦或丙戊酸治疗的患者之间,CDI、SDQ总分及各子量表分数均未观察到统计学显著差异(p>0.05)。一名15岁接受左乙拉西坦治疗的女孩在基线时CDI评分为18,无自杀意念。在1个月随访时,她出现了自杀意念和抑郁,在将左乙拉西坦换为丙戊酸后症状缓解。在其他患者中未观察到其他精神或行为副作用。
左乙拉西坦治疗的心理社会和行为副作用并不常见,且在大多数低剂量儿童中不会出现。在此剂量下,且在3个月后,使用这些特定工具,我们未观察到丙戊酸组和左乙拉西坦治疗组之间存在任何差异。