Neuroscience Center of Excellence, Meyer Children's Hospital, University of Florence, Florence, Italy.
Department of Neurosciences, Psychology, Drug Research, and Child Health, University of Florence, Florence, Italy.
Epilepsia. 2018 Feb;59(2):297-314. doi: 10.1111/epi.13981. Epub 2017 Dec 22.
To estimate the comparative efficacy among antiepileptic drugs in the pediatric population (0-18 years).
Using the Embase and MEDLINE databases, we updated to February 2017 the search strategy of the National Institute for Health and Care Excellence guidelines for epilepsy. We only included randomized clinical trials conducted in children and mixed-age populations. According to the PRISMA network meta-analysis guideline, the study-level quality assessment was made with the Cochrane risk-of-bias tool. Three investigators independently selected articles. The efficacy outcome was considered to be seizure freedom or ≥50% seizure reduction.
We selected 46 randomized clinical trials. A total of 5652 individuals were randomized to 22 antiepileptic drugs and placebo. The point estimates of carbamazepine and lamotrigine efficacy showed their superiority with respect to all comparator antiepileptic drugs for the treatment of newly diagnosed focal epilepsy. In refractory focal epilepsy, levetiracetam (odds ratio [OR] = 3.3, 95% credible interval [CrI] = 1.3-7.6) and perampanel (OR = 2.5, 95% CrI = 1.1-5.8) were more effective compared to placebo. Ethosuximide and valproic acid were both superior to lamotrigine against absence seizures. The OR point estimate showed the superiority of adrenocorticotropic hormone over all comparators in infantile spasms. A wide heterogeneity in the length of follow-up was observed among the studies.
This network meta-analysis suggests that the quality of studies should be improved through the use of comparative designs, relevant outcomes, appropriate follow-up length, and more reliable inclusion criteria.
评估儿科人群(0-18 岁)中抗癫痫药物的相对疗效。
使用 Embase 和 MEDLINE 数据库,我们更新了国家卫生与保健卓越研究所(NICE)癫痫指南的搜索策略,截止日期为 2017 年 2 月。我们仅纳入了在儿童和混合年龄人群中进行的随机临床试验。根据 PRISMA 网络荟萃分析指南,使用 Cochrane 偏倚风险工具对研究水平的质量进行评估。三位研究者独立筛选文章。疗效结果被定义为无发作或发作减少≥50%。
我们共筛选出 46 项随机临床试验,共计 5652 名个体被随机分配至 22 种抗癫痫药物和安慰剂。卡马西平和拉莫三嗪疗效的点估计值表明,在治疗新诊断的局灶性癫痫方面,它们优于所有对照抗癫痫药物。在耐药性局灶性癫痫中,左乙拉西坦(比值比[OR] = 3.3,95%可信区间[CrI] = 1.3-7.6)和吡仑帕奈(OR = 2.5,95% CrI = 1.1-5.8)与安慰剂相比更有效。乙琥胺和丙戊酸对失神发作均优于拉莫三嗪。OR 点估计值表明促肾上腺皮质激素优于所有对照药物在婴儿痉挛中的疗效。研究之间的随访时间长度存在很大的异质性。
这项网络荟萃分析表明,应通过使用对照设计、相关结局、适当的随访时间和更可靠的纳入标准来提高研究的质量。