Melatonin for Acute Treatment of Migraine in Children and Adolescents: A Pilot Randomized Trial

被引:22
作者
Gelfand, Amy A. [1 ]
Ross, Alexandra C. [2 ]
Irwin, Samantha L. [1 ]
Greene, Kaitlin A. [3 ]
Qubty, William F. [4 ]
Allen, I. Elaine [5 ]
机构
[1] UCSF Child & Adolescent Headache Program, Dept Neurol, 550 16th St,4th Floor, San Francisco, CA 94158 USA
[2] UCSF Child & Adolescent Headache Program, Dept Pediat, San Francisco, CA 94158 USA
[3] Oregon Hlth & Sci Univ, Dept Pediat, Div Pediat Neurol, 3181 Sw Sam Jackson Pk Rd, Portland, OR 97201 USA
[4] Univ Texas Austin, Dell Med Sch, Pediat Headache Program, Austin, TX 78712 USA
[5] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA USA
来源
HEADACHE | 2020年 / 60卷 / 08期
关键词
melatonin; migraine; pediatric; POTENTIAL USE; PAIN; SEDATION; PLACEBO; LIFE; AGE;
D O I
10.1111/head.13934
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To determine what dose of melatonin is most effective for treating migraine acutely in children and adolescents. Background Acute migraine medications may not work for all patients and may cause side effects. Melatonin is effective for migraine prevention in adults and has been used acutely for procedural pain in children. Our goal was to determine whether a "high" or "low" dose of melatonin is more effective for treating migraine acutely in youth. Methods In this pilot, randomized, open-label, single-center, dose-finding trial, children and adolescents aged 4-17 years with episodic migraine were randomized to "high-dose" or "low-dose" dose melatonin (<40 kg: 4 mg vs. 1 mg; >= 40 kg: 8 mg vs. 2 mg). The primary outcome measure was change in mean pain score between time 0 and 2 hours. Secondary outcomes included 2-hour pain-relief and pain-freedom rates. Results Eighty-four participants (n = 42 per group) were enrolled in this study. Mean (SD) participant age was 11.8 (3.5) years and 55% (46/84) were female. Mean (SD) headache days/month was 5.6 (3.8). Sixty-six (79%) participants provided outcome data and were included in the analyses,n = 24 in the high-dose group andn = 22 in the low-dose group. The drop-out rate was 43% (18/42) in the high-dose group vs. 48% (20/42) in the low-dose group. Mean (SD) change in pain intensity at 2 hours was -2.7 (2.1) cm in the high-dose group vs. -2.3 (2.1) cm in the low-dose group (p = .581), a difference of 0.4 cm (95% CI: -1.17 to 1.92). Two-hour pain-freedom rate was 41% (7/17) vs. 27% (4/15) in the high-dose vs. low-dose groups (p = .415), and 2-hour pain-relief rate was 94% (16/17) vs. 80% (12/15), (p = .482). There were no serious adverse events. Napping occurred in the majority (67% (14/21) high dose vs. 47% (9/19) low dose). Higher mg/kg dose of melatonin and napping were each independently associated with greater headache benefit. Conclusions As an acute treatment for pediatric migraine, both low and high doses of melatonin were associated with pain reduction; however, study drop-out was high. Higher dose and napping after treatment predicted greater benefit.
引用
收藏
页码:1712 / 1721
页数:10
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