Real-world barriers to health care utilization among people living with migraine: Insights from the All of Us Research Program.

IF 4 2区 医学 Q1 CLINICAL NEUROLOGY
Headache Pub Date : 2025-09-01 Epub Date: 2025-07-15 DOI:10.1111/head.15007
Idris Demirsoy, Richard B Lipton, Ali Ezzati
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引用次数: 0

Abstract

Objectives/background: This study was undertaken to compare health care utilization barriers between participants with medically diagnosed migraine and matched controls without diagnosed migraine. Migraine imposes a significant burden on individuals and on health care systems worldwide. The role of sociodemographic factors and comorbidities in shaping health care utilization for migraine remains insufficiently understood, necessitating further investigation.

Methods: The All of Us Research Program is a large-scale, prospective cohort study funded by the National Institutes of Health. It collects extensive demographic, lifestyle, and health information through self-reports and electronic health records. This analysis uses the Controlled Tier Dataset V7, covering participant data from May 2018 to May 2024. Participants with migraine were identified based on self-reported data from the survey and confirmation of a medical migraine diagnosis through electronic health records using Systematized Nomenclature of Medicine (SNOMED) codes. Additionally, migraine-free controls were propensity-matched to the migraine cases on age, sex, race, and income.

Results: We identified 8346 migraine cases and an equal number of controls. Each group had an average age of 53.3 years and was 87% female. Despite matching for demographic variables and income, people with migraine had significantly more financial, social, and access barriers than those without migraine. There were higher rates of financial difficulties (46.8% vs. 40.3%, p < 0.001) and more transportation issues (9.9% vs. 5.8%, p < 0.001). They also reported more frequent doctor visits within the past 6 months (93.6% vs. 88.9%, p < 0.001) and a greater number of total doctor visits annually compared to those free of diagnosed migraine (31.1% vs. 17.4%, p < 0.001).

Conclusion: This study highlights the significant financial, social, and access barriers faced by participants with migraine, alongside higher health care utilization, compared to those without diagnosed migraine despite matching for demographic variables and income. These findings underscore the substantial burden of migraine and emphasize the urgent need for targeted interventions to enhance health care accessibility and reduce the burden on affected individuals. These data do not capture the burden of undiagnosed migraine due to the method of case ascertainment.

现实世界中偏头痛患者医疗保健利用的障碍:来自我们所有人研究项目的见解。
目的/背景:本研究旨在比较医学诊断为偏头痛的参与者和未诊断为偏头痛的对照组之间的医疗保健利用障碍。偏头痛给全世界的个人和卫生保健系统带来了沉重的负担。社会人口因素和合并症在影响偏头痛医疗保健利用方面的作用仍然不够清楚,需要进一步调查。方法:“我们所有人研究计划”是一项由美国国立卫生研究院资助的大规模前瞻性队列研究。它通过自我报告和电子健康记录收集广泛的人口统计、生活方式和健康信息。本分析使用受控层数据集V7,涵盖2018年5月至2024年5月的参与者数据。偏头痛患者是根据调查中自我报告的数据和通过使用系统化医学命名法(SNOMED)代码的电子健康记录确认的医学偏头痛诊断来确定的。此外,无偏头痛的对照组在年龄、性别、种族和收入方面与偏头痛患者的倾向相匹配。结果:我们确定了8346例偏头痛病例和相同数量的对照组。每组平均年龄53.3岁,87%为女性。尽管人口统计变量和收入相匹配,偏头痛患者明显比没有偏头痛的人有更多的经济、社会和访问障碍。结论:尽管与人口变量和收入相匹配,但与未诊断为偏头痛的患者相比,该研究强调了偏头痛患者面临的重大财务、社会和获取障碍,以及更高的医疗保健利用率。这些发现强调了偏头痛的巨大负担,并强调迫切需要有针对性的干预措施,以提高卫生保健的可及性,减轻受影响个体的负担。由于病例确定的方法,这些数据没有捕捉到未确诊偏头痛的负担。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Headache
Headache 医学-临床神经学
CiteScore
9.40
自引率
10.00%
发文量
172
审稿时长
3-8 weeks
期刊介绍: Headache publishes original articles on all aspects of head and face pain including communications on clinical and basic research, diagnosis and management, epidemiology, genetics, and pathophysiology of primary and secondary headaches, cranial neuralgias, and pains referred to the head and face. Monthly issues feature case reports, short communications, review articles, letters to the editor, and news items regarding AHS plus medicolegal and socioeconomic aspects of head pain. This is the official journal of the American Headache Society.
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