Ubrogepant users' real-world experience: Patients on ubrogepant, characteristics and outcomes (UNIVERSE) study.

IF 5.4 2区 医学 Q1 CLINICAL NEUROLOGY Headache Pub Date : 2024-11-01 Epub Date: 2024-09-26 DOI:10.1111/head.14839
Anand R Shewale, Weijie Poh, Michael L Reed, Jinjie Liu, Francois Cadiou, Ali Ezzati, Kate Burslem, Shivaji Manthena, Richard B Lipton
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Abstract

Objective: To assess the real-world effectiveness of ubrogepant by evaluating self-reported satisfaction with pain relief, ability to think clearly, and return to normal function in individuals who had used ubrogepant to treat a migraine episode within the preceding 14 days.

Background: Ubrogepant is an oral calcitonin gene-related peptide receptor antagonist approved for the acute treatment of migraine in adults. Few studies have evaluated the real-world effectiveness of ubrogepant.

Methods: The UNIVERSE study was an observational, cross-sectional survey conducted between February 2021 and April 2021 in US adult Migraine Buddy application (app) users currently treated with ubrogepant. Individuals who were 18 years of age or older and reported at least one dose of ubrogepant in the previous 14 days completed a 30-question survey in the app. The survey assessed respondent demographics, migraine history, acute treatment patterns, and treatment satisfaction with ubrogepant. Respondents also reported prior acute medication use and reasons for switching to ubrogepant.

Results: Of the 1303 ubrogepant users contacted, 302 (23.2%; 50 mg, 120 participants; 100 mg, 182 participants) were included in this study. The mean (standard deviation) age was 41.9 (11.2) years, and 90.1% (272/302) were female. Satisfaction with migraine relief at 2, 4, and 24 h post-dose was reported by 75.8% (229/302), 83.4% (252/302), and 78.5% (237/302) of participants, respectively. Satisfaction with the ability to think clearly after taking ubrogepant was reported by 85.1% (257/302) of participants, and 83.8% (253/302) were satisfied with their ability to return to normal function. Furthermore, 90.7% (274/302) of participants reported that they were likely to continue using ubrogepant to treat their migraine. Most participants (n = 264 [87%]) reported switching to ubrogepant due to inadequate treatment response with their previous treatment. In this subgroup, comparable outcomes were observed with respect to satisfaction with migraine relief, ability to think clearly, and return to normal function.

Conclusions: Ubrogepant demonstrated real-world effectiveness in the acute treatment of migraine, as evidenced by high levels of treatment satisfaction and a strong indication of their intent to continue using the medication.

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优搏定使用者的真实体验:使用优搏定的患者、特征和结果(UNIVERSE)研究。
目的通过评估曾在14天内使用优搏定治疗偏头痛发作的患者对疼痛缓解的自述满意度、清晰思考的能力以及恢复正常功能的情况,评估优搏定的实际疗效:背景:乌溴盖坦是一种口服降钙素基因相关肽受体拮抗剂,已被批准用于成人偏头痛的急性治疗。很少有研究对乌布格潘的实际疗效进行评估:UNIVERSE 研究是一项观察性横断面调查,于 2021 年 2 月至 2021 年 4 月间在目前使用 ubrogepant 治疗偏头痛的美国成人偏头痛 Buddy 应用程序(app)用户中进行。年龄在 18 周岁或以上并报告在过去 14 天内至少服用过一次乌罗盖板的用户在应用程序中完成了一项包含 30 个问题的调查。该调查评估了受访者的人口统计学特征、偏头痛病史、急性治疗模式以及对乌罗盖板的治疗满意度。受访者还报告了之前的急性期用药情况以及改用乌罗盖板的原因:在所联系的 1303 名优氯吉潘使用者中,有 302 人(23.2%;50 毫克,120 人;100 毫克,182 人)被纳入本研究。平均(标准差)年龄为 41.9(11.2)岁,90.1%(272/302)为女性。75.8%(229/302)、83.4%(252/302)和78.5%(237/302)的参与者对服药后2、4和24小时偏头痛缓解情况表示满意。85.1%(257/302)的受试者对服用乌洛格班后能否清晰思考表示满意,83.8%(253/302)的受试者对能否恢复正常功能表示满意。此外,90.7%(274/302)的参与者表示他们可能会继续使用优搏定治疗偏头痛。大多数参试者(n = 264 [87%])表示,由于之前的治疗效果不佳而改用优搏定。在这一分组中,观察到的结果与偏头痛缓解满意度、清晰思考能力和恢复正常功能方面的结果相当:优搏定在偏头痛的急性期治疗中显示出了实际疗效,患者对治疗的满意度很高,并强烈表示愿意继续用药。
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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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