Khodavirdi Ani C, Multani Jasjit K, Oh Sam S, Vuvu Fiston, Bensink Mark E, Stockl Karen M, Hawkins Kevin, Chiang Chia-Chun, Green A Laine, Tepper Stewart J
Amgen Inc., Thousand Oaks, CA, United States.
IQVIA, Plymouth, PA, United States.
Front Neurol. 2024 Aug 6;15:1433423. doi: 10.3389/fneur.2024.1433423. eCollection 2024.
Migraine is a debilitating neurological disorder, with a wide range of symptoms and disease burden, underscoring the heterogeneity of patients' disease characteristics and treatment needs. To characterize the profile of migraine patients in the US who may be eligible for preventive treatment with an anti-CGRP pathway mAb and to better understand treatment patterns and real-world use of acute and preventive medications for migraine, we conducted a retrospective cohort study of adult patients.
These patients were identified as having migraine using diagnosis codes or migraine-specific medication use (first = index) in the IQVIA PharMetrics® Plus database. Patients were required to have ≥ 12 months of continuous enrollment in medical and pharmacy benefits prior to index (baseline) and after index (follow-up). Patients were stratified into chronic migraine (CM) and non-chronic migraine (non-CM) by diagnosis codes. Based on acute migraine-specific medication dispensing data in the follow-up period, non-CM patients were divided into 3 cohorts: highest, middle, and lowest tertile of total units of dispensed acute migraine-specific medication (gepants, ditans, ergot derivatives, and triptans). Migraine medication use was captured in the baseline and follow-up periods.
A total of 22,584 CM and 216,807 non-CM patients (72,269 patients in each tertile) were identified and included in the study. Over the follow-up, CM patients had a mean of 70 units of acute migraine-specific medications dispensed, while the highest, middle, and lowest tertile of non-CM patients had a mean of 92, 29, and 10 units, respectively. Anti-calcitonin gene-related peptide pathway mAbs were dispensed for 28.9% of CM patients, and for 6.9%, 4.1%, and 2.9% of non-CM patients in the highest, middle, and lowest tertiles, respectively.
A lower proportion of non-CM patients had use of anti-calcitonin gene-related peptide pathway mAbs compared to CM patients, confirming the unmet need with appropriate preventive medication. There appears to be a persistent gap in management of patients without a diagnosis of CM who are dispensed high quantities of acute migraine-specific medications.
偏头痛是一种使人衰弱的神经系统疾病,具有广泛的症状和疾病负担,突出了患者疾病特征和治疗需求的异质性。为了描述美国可能有资格接受抗降钙素基因相关肽(CGRP)通路单克隆抗体预防性治疗的偏头痛患者的特征,并更好地了解偏头痛急性和预防性药物的治疗模式及实际应用情况,我们对成年患者进行了一项回顾性队列研究。
在IQVIA PharMetrics® Plus数据库中,通过诊断编码或使用偏头痛特异性药物(首次使用=索引)来确定这些患者患有偏头痛。患者在索引(基线)之前和索引(随访)之后需要连续登记医疗和药房福利≥12个月。根据诊断编码将患者分为慢性偏头痛(CM)和非慢性偏头痛(非CM)。根据随访期间急性偏头痛特异性药物的配药数据,将非CM患者分为3个队列:配药急性偏头痛特异性药物总单位数的最高三分位数、中间三分位数和最低三分位数( gepants、双氢麦角胺类、麦角衍生物和曲坦类)。在基线期和随访期记录偏头痛药物的使用情况。
共识别出22584例CM患者和216807例非CM患者(每个三分位数各72269例)并纳入研究。在随访期间,CM患者平均配药70单位急性偏头痛特异性药物,而非CM患者的最高、中间和最低三分位数分别平均配药92、29和10单位。抗降钙素基因相关肽通路单克隆抗体分别用于28.9%的CM患者,以及最高、中间和最低三分位数中6.