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乌布罗苷肽真实世界应用经验:乌布罗苷肽治疗患者的特征和结局(UNIVERSE)研究。

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

机构信息

AbbVie, North Chicago, Illinois, USA.

Healint Pte Ltd, Singapore, Singapore.

出版信息

Headache. 2024 Nov-Dec;64(10):1244-1252. doi: 10.1111/head.14839. Epub 2024 Sep 26.

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.

摘要

目的

通过评估先前在 14 天内使用ubrogepant 治疗偏头痛发作的个体对疼痛缓解、思维清晰能力和恢复正常功能的自我报告满意度,评估 ubrogepant 的实际疗效。

背景

ubrogepant 是一种口服降钙素基因相关肽受体拮抗剂,已获批准用于成人偏头痛的急性治疗。目前,仅有少数研究评估了 ubrogepant 的实际疗效。

方法

UNIVERSE 研究是一项在美国偏头痛 Buddy 应用程序(app)中正在接受 ubrogepant 治疗的成年偏头痛患者中开展的观察性、横断面调查,于 2021 年 2 月至 2021 年 4 月进行。年龄在 18 岁及以上且在过去 14 天内至少使用过一次 ubrogepant 的患者在应用程序中完成了 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 ubrogepant 的治疗满意度。受访者还报告了先前急性治疗药物的使用情况和改用 ubrogepant 的原因。

结果

在联系的 1303 名 ubrogepant 用户中,302 名(23.2%;50mg 组 120 名参与者;100mg 组 182 名参与者)被纳入本研究。患者的平均(标准差)年龄为 41.9(11.2)岁,90.1%(272/302)为女性。分别有 75.8%(229/302)、83.4%(252/302)和 78.5%(237/302)的参与者报告偏头痛缓解在 2、4 和 24 小时时的满意度;分别有 85.1%(257/302)和 83.8%(253/302)的参与者报告服用 ubrogepant 后思维清晰的满意度和恢复正常功能的满意度。此外,90.7%(274/302)的参与者表示他们可能会继续使用 ubrogepant 治疗偏头痛。大多数参与者(n=264[87%])报告称,改用 ubrogepant 是因为他们之前的治疗没有达到足够的治疗反应。在该亚组中,在偏头痛缓解、思维清晰和恢复正常功能的满意度方面观察到了类似的结果。

结论

ubrogepant 在偏头痛的急性治疗中显示出了实际疗效,这表现在其治疗满意度高,且表明患者很可能会继续使用该药物。

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