Division of Child Neurology, Department of Neurology, University of Washington School of Medicine and the Seattle Children's Research Institute, Center for Integrative Brain Research, Seattle, Washington.
Department of Pediatric Emergency Medicine, University of Washington, Seattle Children's Hospital, Seattle, Washington.
Pediatr Neurol. 2023 May;142:68-75. doi: 10.1016/j.pediatrneurol.2023.01.016. Epub 2023 Feb 4.
Headache is a common presenting condition for patients seen in the pediatric emergency department (ED). Intranasal (IN) sumatriptan is a well-tolerated and safe abortive treatment for migraine headache, but it is infrequently administered in pediatric EDs. In this study we characterize an ED migraine pathway that uses IN sumatriptan as a first-line treatment.
We performed retrospective chart analysis from a single center, reviewing a cohort of patients treated on an ED migraine pathway between October 2016 and February 2020. We reviewed patient demographics, clinical characteristics, treatment patterns, change in pain scores, sumatriptan prescriptions at discharge, length of stay (LOS), ED charges, and unexpected return visits.
A total of 558 patients (aged six to 21 years, 66% female) were included in this study. Overall, the median pretreatment pain score was 7 (interquartile range [IQR]: 5 to 8) and the median post-treatment pain score was 2 (IQR: 0 to 4). Forty-eight percent of patients received IN sumatriptan in the ED, and 36% of those who received sumatriptan were prescribed oral sumatriptan at discharge. When intravenous (IV) access was obtained for headache management, this was associated with a significantly longer LOS and higher ED charges.
IN sumatriptan shows promise as a feasible and potentially effective first-line treatment for pediatric migraine in the ED that could reduce the need for IV therapies, shorten LOS, and lower ED charges. Further research is needed to determine the efficacy of IN sumatriptan relative to other common first-line therapies used to treat pediatric migraine in the ED.
头痛是儿科急诊(ED)就诊患者常见的主要症状。鼻内(IN)舒马曲坦是一种耐受性好且安全的偏头痛治疗药物,但在儿科 ED 中很少使用。在这项研究中,我们描述了一种使用 IN 舒马曲坦作为一线治疗的 ED 偏头痛治疗途径。
我们对 2016 年 10 月至 2020 年 2 月期间在 ED 偏头痛治疗途径上接受治疗的患者进行了单中心回顾性图表分析。我们回顾了患者的人口统计学特征、临床特征、治疗模式、疼痛评分变化、出院时舒马曲坦处方、住院时间(LOS)、ED 费用以及意外复诊情况。
本研究共纳入 558 例(年龄 6 至 21 岁,66%为女性)患者。总体而言,预处理疼痛评分中位数为 7(四分位距[IQR]:5 至 8),治疗后疼痛评分中位数为 2(IQR:0 至 4)。48%的患者在 ED 接受了 IN 舒马曲坦治疗,接受舒马曲坦治疗的患者中有 36%在出院时开具了口服舒马曲坦。当为头痛管理获得静脉(IV)通路时,这与 LOS 显著延长和 ED 费用增加相关。
IN 舒马曲坦有望成为 ED 中治疗儿科偏头痛的一种可行且潜在有效的一线治疗方法,可减少对 IV 治疗的需求、缩短 LOS 并降低 ED 费用。需要进一步研究来确定 IN 舒马曲坦相对于 ED 中用于治疗儿科偏头痛的其他常用一线治疗药物的疗效。