与三级头痛中心偏头痛药物处方相关的社会经济因素:回顾性队列分析。

IF 3.2 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-10-01 Epub Date: 2025-07-25 DOI:10.1212/CPJ.0000000000200517
Arathi S Nandyala, Kenneth Tan, Benjamin Africk, Anna Graber-Naidich, Niushen Zhang, Zihuai He, Leon S Moskatel
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引用次数: 0

摘要

背景和目的:影响偏头痛药物处方的社会经济和人口因素尚未得到充分研究。了解这些因素对于解决健康问题至关重要。我们使用三级头痛中心的处方数据库来评估与急性和预防性偏头痛药物处方相关的人口统计学和社会经济因素,以及影响新型偏头痛药物推广的因素。方法:我们对通过斯坦福头痛诊所接受治疗的患者进行了回顾性队列分析,使用的数据来自斯坦福观察性医疗结果合作伙伴共同数据模型的未识别实例。我们纳入了加州的患者,他们被诊断为慢性偏头痛,并在2018年至2022年期间从我们的诊所接受了至少一个处方。评估了处方的类型和数量,以及人口因素(年龄、性别、种族、民族和邮政编码收入四分位数)。结果:符合纳入标准的患者共4213例,其中女性3349例(79.5%),男性863例(20.5%),平均年龄44.6±14.7岁。我们的小组主要是白人和非西班牙裔/非拉丁裔(2381 /4213,56.5%),来自邮政编码的中位数收入从77,250美元到236,912美元(2046/3298,62.0%)。年龄、性别和种族都被发现是患者选择急性和预防性药物的统计学显著因素。邮政编码收入四分位数在急性和预防性药物的处方变化中发挥的作用有限。对于那些接受降钙素基因相关肽(CGRP)单克隆抗体处方的患者来说,种族也是一个统计上显著的因素。同样,性别、种族和邮政编码收入四分位数都是CGRP单克隆抗体和基因推广的因素(均p < 0.05),但年龄不是(p分别= 0.722和p = 0.057)。第二和第三邮政编码收入四分位数的最低处方率CGRP单克隆抗体和基因在他们的推出。讨论:在接受药物治疗的患者中,发现了性别、种族和邮政编码收入四分位数的差异,以及急性和预防性偏头痛药物的处方。这可能反映了一些群体在与我们的诊所建立之前可能接受较少的头痛特异性护理。未来的研究将寻求更清楚地阐明这一现象的根本原因,以实现解决方案并确保公平护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Socioeconomic Factors Associated With Migraine Medication Prescription at a Tertiary Headache Center: A Retrospective Cohort Analysis.

Background and objectives: The socioeconomic and demographic factors affecting the prescription of migraine medications are underexplored. Understanding these factors is critical to addressing health. We used our tertiary headache center's prescription database to assess the demographic and socioeconomic factors associated with the prescription of acute and preventive migraine medications and the factors affecting the rollout of novel migraine medications.

Methods: We performed a retrospective cohort analysis using aggregated deidentified data of patients who had received care through the Stanford Headache Clinic using data adapted from the Stanford deidentified instance of the Observational Medical Outcomes Partnership Common Data Model. We included patients in California who had received a diagnosis of chronic migraine and had received at least 1 prescription from our clinic between 2018 and 2022. The types and volumes of prescriptions were assessed, as well as demographic factors (age, sex, race ethnicity, and zip code income quartile).

Results: A total of 4,213 patients met inclusion criteria, of whom 3,349 (79.5%) were women and 863 (20.5%) were men, with a mean age of 44.6 ± 14.7 years. Our group was predominantly White and non-Hispanic/non-Latino (2,381/4213, 56.5%) and came from zip codes whose median income ranged from $77,250 to $236,912 (2046/3298, 62.0%). Age, sex, and race-ethnicity were all found to be statistically significant factors in the selection of both acute and preventive medications for patients. Zip code income quartile played a limited role in prescription variation for both acute and preventive medications. Race-ethnicity was also a statistically significant factor for those who received a prescription for a calcitonin gene-related peptide (CGRP) monoclonal antibody and a gepant. Similarly, sex, race-ethnicity, and zip code income quartile were all factors in the rollout of the CGRP monoclonal antibodies and gepants (all p < 0.05), but age was not (p = 0.722 and p = 0.057, respectively). The second and third zip code income quartiles had the lowest prescription rates of the CGRP monoclonal antibodies and gepants during their rollout.

Discussion: Disparities in sex, race-ethnicity, and zip code income quartile were found among those who received medications and which acute and preventive migraine medications were prescribed. This may reflect that some groups may have received less headache-specific care before establishing with our clinic. Future research will seek to better illuminate the underlying reasons for this more clearly to enable solutions and ensure equitable care.

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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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