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不适用于曲坦类药物治疗的偏头痛患者的相对频率、特征及疾病负担:一项系统文献综述

Relative frequency, characteristics, and disease burden of patients with migraine unsuitable for triptan treatment: A systematic literature review.

作者信息

Lipton Richard B, Gendolla Astrid, Abraham Lucy, Jenkins Aaron, Telfort Jersen, Blakeman Karin Hygge, Saccone Phillip A, Pustulka Iwona, Fotheringham Iain, Engh Anita

机构信息

Albert Einstein College of Medicine, Bronx, New York, USA.

Montefiore Medical Center, Bronx, New York, USA.

出版信息

Headache. 2025 Jan;65(1):164-179. doi: 10.1111/head.14854. Epub 2024 Nov 27.

Abstract

OBJECTIVE

This review was conducted to systematically identify evidence characterizing patients with migraine who are unsuitable for triptans.

BACKGROUND

Triptans are not suitable as first-line treatment for all patients with migraine due to contraindications, lack of efficacy, and/or poor tolerability. However, there is debate about the frequency and characteristics of these patients and the burden they experience.

METHODS

MEDLINE, Embase, and conference abstracts (2011-2022) were reviewed for evidence on patients with migraine unsuitable for triptans for any reason. Data from publications describing the frequency and characteristics of this group, as well as the clinical, humanistic, or economic burden of disease in this population, were extracted.

RESULTS

Of 1460 records screened, 29 publications met inclusion criteria. Persistence with triptans was low; 51%-66% of patients starting a new triptan did not refill it, and 43%-100% discontinued their initial triptan over 2 years. In one study, 14% of patients with migraine reported prior discontinuation/failure of ≥ 2 triptans due to inadequate efficacy or poor tolerability. Up to 15% of patients with migraine had triptan contraindications, and ≥ 20% of patients receiving triptans had contraindications. In four studies, 10%-44% of patients who tried triptans had insufficient response, although definitions varied. Patients who achieved a sufficient response typically did so with their first triptan; few became responders with additional triptans. Of patients who did not respond to one to two triptans and received another, 45% were dissatisfied with the final triptan. Approximately half of patients who tried two to three triptans had an insufficient response. Greater disability, impact of disease, and depression were reported in triptan discontinuers compared to those with sustained use. Worse quality of life scores and utility values were reported in triptan insufficient versus sufficient responders, as were greater migraine-related costs, work impairment, and health-care resource utilization.

CONCLUSION

The total population of patients unsuitable for triptans is uncertain, but the literature highlights a large group who cannot or do not persist with triptans, and current evidence suggests a high burden in this population and an unmet need for new therapeutic options. Further research is needed to determine the frequency of unsuitability for triptans more precisely and to assess the associated burden.

摘要

目的

本综述旨在系统地识别那些不适合使用曲坦类药物治疗的偏头痛患者的特征证据。

背景

由于存在禁忌证、疗效不佳和/或耐受性差等原因,曲坦类药物并不适合所有偏头痛患者作为一线治疗药物。然而,关于这些患者的频率和特征以及他们所承受的负担仍存在争议。

方法

检索MEDLINE、Embase和会议摘要(2011 - 2022年),以获取关于因任何原因不适合使用曲坦类药物的偏头痛患者的证据。从描述该群体频率和特征以及该人群疾病的临床、人文或经济负担的出版物中提取数据。

结果

在筛选的1460条记录中,29篇出版物符合纳入标准。曲坦类药物的持续使用率较低;开始使用新曲坦类药物的患者中,51% - 66%没有再次配药,43% - 100%在2年期间停用了最初使用的曲坦类药物。在一项研究中,14%的偏头痛患者报告因疗效不佳或耐受性差而曾停用/使用≥2种曲坦类药物且治疗失败。高达15%的偏头痛患者有曲坦类药物禁忌证,接受曲坦类药物治疗的患者中≥20%有禁忌证。在四项研究中,尝试使用曲坦类药物的患者中有10% - 44%反应不足,尽管定义有所不同。获得充分反应的患者通常在首次使用曲坦类药物时就有反应;很少有患者通过额外使用曲坦类药物而成为有反应者。在对一到两种曲坦类药物无反应并接受另一种药物治疗的患者中,45%对最终使用的曲坦类药物不满意。尝试使用两到三种曲坦类药物的患者中约有一半反应不足。与持续使用者相比,停用曲坦类药物的患者报告有更大的残疾、疾病影响和抑郁。曲坦类药物反应不足者与反应充分者相比,生活质量评分和效用值更差,偏头痛相关成本、工作障碍和医疗资源利用也更高。

结论

不适合使用曲坦类药物的患者总数尚不确定,但文献强调了一大群无法或不再坚持使用曲坦类药物的患者,目前的证据表明该人群负担较重,对新治疗选择的需求未得到满足。需要进一步研究以更精确地确定不适合使用曲坦类药物的频率,并评估相关负担。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8967/11726002/dd977d4de68c/HEAD-65-164-g006.jpg

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