Headache Department, Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.
School of Medicine, Alborz University of Medical Sciences, Karaj, Iran.
JAMA Netw Open. 2024 Oct 1;7(10):e2438666. doi: 10.1001/jamanetworkopen.2024.38666.
Pediatric migraine substantially impacts quality of life and academic performance among children and adolescents. Understanding the efficacy and safety of pharmacological interventions for migraine prophylaxis in this population is crucial for developing effective treatment strategies.
To conduct a comprehensive network meta-analysis to evaluate the efficacy and safety associated with pharmacological treatments for pediatric migraine prophylaxis among pediatric patients with a migraine diagnosis and assess interventions involving various oral pharmacological interventions compared with each other and placebo.
PubMed, Embase, and SCOPUS were searched for publications up to September 2023. Search terms and indexing were chosen to encompass relevant studies, focusing on randomized clinical trials in pediatric migraine prophylaxis.
Inclusion criteria targeted randomized clinical trials involving pediatric patients with migraine. Studies were selected based on their examination of oral pharmacological interventions. The search yielded an initial 9162 citations.
Data extraction adhered to Preferred Reporting Items for Systematic Reviews and Meta-Analyses reporting guidelines. Five investigators independently extracted study data into a spreadsheet in duplicate. Study-level estimates were calculated, employing a random-effects model for primary and secondary outcomes due to identified heterogeneity. Data analysis was conducted from December 2023 to March 2024.
The primary outcome was migraine frequency (number of attacks per month). Secondary outcomes included a 50% or greater responder rate, headache duration, headache intensity, and disability (assessed by pediatrics migraine-specific disability tool). Adverse events were also evaluated.
The analysis incorporated 45 trials with 3771 participants. Compared with placebo, pregabalin (ratio of means [RoM], 0.38; 95% CI, 0.18-0.79) and topiramate with vitamin D3 (RoM, 0.44; 95% CI, 0.30-0.65) were associated with reduction in migraine frequency. Flunarizine (RoM, 0.46; 95% CI, 0.26-0.81), levetiracetam (RoM, 0.47; 95% CI, 0.30-0.72), riboflavin (RoM, 0.50; 95% CI, 0.32-0.77), cinnarizine (RoM, 0.64; 95% CI, 0.46-0.88), topiramate (RoM, 0.70; 95% CI, 0.55-0.89), and amitriptyline (RoM, 0.73; 95% CI, 0.54-0.97) were also associated with reduction in migraine frequency, but these findings were drawn from individual studies. For the 50% or greater responder rate, flunarizine and α-lipoic acid (risk ratio [RR], 8.73; 95% CI, 2.44-31.20), flunarizine (RR, 4.00; 95% CI, 1.38-11.55), pregabalin (RR, 1.88; 95% CI, 1.13-3.14), and cinnarizine (RR, 1.46; 95% CI, 1.04-2.05) were associated with significantly greater effectiveness than placebo. Compared with placebo, propranolol and cinnarizine (RoM, 0.45; 95% CI, 0.28-0.72), pregabalin (RoM, 0.57; 95% CI, 0.33-0.96), valproate (RoM, 0.60; 95% CI, 0.49-0.72), levetiracetam (RoM, 0.62; 95% CI, 0.50-0.77), and cinnarizine (RoM, 0.64; 95% CI, 0.54-0.76) were significantly associated with reduction in headache intensity. However, no treatments were associated with significant improvements in quality of life or reduction of the duration of migraine attacks. Adverse events were higher with amitriptyline (RR, 3.81; 95% CI, 1.41-10.32), topiramate (RR, 4.34; 95% CI, 1.60-11.75), and valproate (RR, 5.93; 95% CI, 1.93-18.23) compared with placebo.
In this network meta-analysis of randomized clinical trials, topiramate and pregabalin were associated with reduction in headache frequency and intensity. Although there were also other drugs that showed statistically significant results (flunarizine, riboflavin, amitriptyline, and cinnarizine), more studies were required for a robust conclusion. None of the drugs were associated with improved quality of life or attack duration, underscoring the need for further research to develop more comprehensive treatment strategies and explore the potential of combination therapies, especially those involving vitamins. Future studies should focus on validating these findings and expanding the treatment landscape for pediatric migraine management.
儿童偏头痛会极大地影响儿童和青少年的生活质量和学业成绩。了解儿科偏头痛预防中各种药理学干预措施的疗效和安全性对于制定有效的治疗策略至关重要。
进行全面的网络荟萃分析,评估儿科偏头痛预防中各种药理学治疗的疗效和安全性,并评估各种口服药理学干预措施彼此之间以及与安慰剂相比的干预措施。
截至 2023 年 9 月,在 PubMed、Embase 和 SCOPUS 上搜索了出版物。搜索术语和索引的选择旨在涵盖相关研究,重点是儿科偏头痛预防的随机临床试验。
纳入标准针对有偏头痛诊断的儿科患者的随机临床试验,研究涉及口服药理学干预措施。最初搜索产生了 9162 条引文。
数据提取符合系统评价和荟萃分析报告的首选报告项目指南。五名调查员独立地将研究数据复制到电子表格中。由于发现存在异质性,因此使用随机效应模型计算了研究水平的估计值,以进行主要和次要结局的分析。数据分析于 2023 年 12 月至 2024 年 3 月进行。
主要结局是偏头痛发作频率(每月发作次数)。次要结局包括 50%或更高的应答率、头痛持续时间、头痛强度和残疾(使用儿科偏头痛特异性残疾工具评估)。还评估了不良事件。
该分析纳入了 45 项试验,涉及 3771 名参与者。与安慰剂相比,普瑞巴林(均数比[RoM],0.38;95%置信区间[CI],0.18-0.79)和托吡酯加维生素 D3(RoM,0.44;95%CI,0.30-0.65)与偏头痛发作频率降低相关。氟桂利嗪(RoM,0.46;95%CI,0.26-0.81)、左乙拉西坦(RoM,0.47;95%CI,0.30-0.72)、核黄素(RoM,0.50;95%CI,0.32-0.77)、桂利嗪(RoM,0.64;95%CI,0.46-0.88)、托吡酯(RoM,0.70;95%CI,0.55-0.89)和阿米替林(RoM,0.73;95%CI,0.54-0.97)也与偏头痛发作频率降低相关,但这些发现来自于个别研究。对于 50%或更高的应答率,氟桂利嗪和α-硫辛酸(风险比[RR],8.73;95%CI,2.44-31.20)、氟桂利嗪(RR,4.00;95%CI,1.38-11.55)、普瑞巴林(RR,1.88;95%CI,1.13-3.14)和桂利嗪(RR,1.46;95%CI,1.04-2.05)与安慰剂相比,有效性显著更高。与安慰剂相比,普萘洛尔和桂利嗪(RoM,0.45;95%CI,0.28-0.72)、普瑞巴林(RoM,0.57;95%CI,0.33-0.96)、丙戊酸钠(RoM,0.60;95%CI,0.49-0.72)、左乙拉西坦(RoM,0.62;95%CI,0.50-0.77)和桂利嗪(RoM,0.64;95%CI,0.54-0.76)与头痛强度降低显著相关。然而,没有治疗方法与生活质量的显著改善或偏头痛发作持续时间的缩短相关。与安慰剂相比,阿米替林(RR,3.81;95%CI,1.41-10.32)、托吡酯(RR,4.34;95%CI,1.60-11.75)和丙戊酸钠(RR,5.93;95%CI,1.93-18.23)的不良事件发生率更高。
在这项针对随机临床试验的网络荟萃分析中,托吡酯和普瑞巴林与头痛频率和强度降低相关。尽管还有其他一些药物显示出统计学上显著的结果(氟桂利嗪、核黄素、阿米替林和桂利嗪),但需要更多的研究来得出稳健的结论。没有一种药物与改善生活质量或发作持续时间相关,这强调了需要进一步研究以制定更全面的治疗策略,并探索联合治疗的潜力,特别是涉及维生素的治疗。未来的研究应侧重于验证这些发现,并扩大儿科偏头痛管理的治疗范围。