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一项关于美国接受fremanezumab治疗的患者急性和预防性药物使用、依从性及持续性的真实世界研究。

A real-world study of acute and preventive medication use, adherence, and persistence in patients prescribed fremanezumab in the United States.

作者信息

Krasenbaum Lynda J, Pedarla Vasantha L, Thompson Stephen F, Tangirala Krishna, Cohen Joshua M, Driessen Maurice T

机构信息

Teva Pharmaceutical Industries, West Chester, PA, USA.

STATinMED Research, Ann Arbor, MI, USA.

出版信息

J Headache Pain. 2022 May 4;23(1):54. doi: 10.1186/s10194-022-01413-z.

Abstract

BACKGROUND

Following approval of fremanezumab for the prevention of migraine in adults, health care decision makers are interested in understanding real-world clinical characteristics and treatment patterns among patients initiating fremanezumab therapy.

METHODS

Data were obtained for this retrospective (pre-post) study from the Veradigm Health Insights database. The study period was January 1, 2014, to June 30, 2019. Patients were included if they were aged ≥ 18 years; had ≥ 1 migraine diagnosis during the study period; and had a medication record for fremanezumab on or after diagnosis during the identification period (September 1, 2018-December 31, 2018). Treatment patterns, including adherence, persistence, and utilization of acute and preventive migraine medication prescriptions, were evaluated.

RESULTS

Of 987 patients initiating fremanezumab during the study period, 738 (74.8%) were adherent to fremanezumab by proportion of days covered (PDC; ≥ 80%) and 780 (79.0%) were adherent by medication possession ratio (MPR; ≥ 80%). A total of 746 (75.6%) patients were persistent for ≥ 6 months. Quarterly fremanezumab (n = 186) was associated with higher rates of adherence versus monthly fremanezumab (n = 801) by PDC (quarterly, 91.3%; monthly, 84.9%; P < 0.001) and MPR (quarterly, 92.2%; monthly, 87.9%; P = 0.006) and higher persistence at ≥ 6 months (quarterly, 82.8%; monthly, 73.9%; P = 0.011). After fremanezumab initiation, patients who were persistent for ≥ 6 months experienced significant reductions from baseline in the mean monthly number of acute and preventive migraine medication prescriptions (P < 0.001). Subgroup analyses in patients with comorbid depression and anxiety showed meaningful real-world benefits based on significant reductions in the number of patients who were prescribed antidepressants (baseline, 68.6%; follow-up, 56.4%; P = 0.0025) and anxiolytic medications (baseline, 55.0%; follow-up, 47.2%; P = 0.037), respectively. In a subgroup of patients with comorbid hypertension at baseline, fremanezumab treatment resulted in nonsignificant reductions in blood pressure.

CONCLUSIONS

Overall, adherence and persistence to fremanezumab in this real-world study was high in patients with migraine, with higher rates observed for quarterly fremanezumab. Patients who were persistent for ≥ 6 months experienced significant reductions in acute and preventive migraine medication use, while a subgroup of migraine patients with comorbid depression and anxiety at baseline showed significant reductions in antidepressant and anxiolytic medication use.

摘要

背景

在成人偏头痛预防药物fremanezumab获批后,医疗保健决策者有兴趣了解开始使用fremanezumab治疗的患者的真实世界临床特征和治疗模式。

方法

本回顾性(前后对照)研究的数据来自Veradigm Health Insights数据库。研究期间为2014年1月1日至2019年6月30日。纳入标准为年龄≥18岁;在研究期间有≥1次偏头痛诊断;在识别期(2018年9月1日至2018年12月31日)内诊断后有fremanezumab用药记录。评估了治疗模式,包括依从性、持续性以及急性和预防性偏头痛药物处方的使用情况。

结果

在研究期间开始使用fremanezumab的987例患者中,按覆盖天数比例(PDC;≥80%)计算,738例(74.8%)患者对fremanezumab依从,按药物持有率(MPR;≥80%)计算,780例(79.0%)患者依从。共有746例(75.6%)患者持续使用≥6个月。按PDC计算,每季度使用fremanezumab(n = 186)与每月使用fremanezumab(n = 801)相比,依从率更高(每季度为91.3%,每月为84.9%;P < 0.001),按MPR计算也是如此(每季度为92.2%,每月为87.9%;P = 0.006),且在≥6个月时持续性更高(每季度为82.8%,每月为73.9%;P = 0.011)。开始使用fremanezumab后,持续使用≥6个月的患者每月急性和预防性偏头痛药物处方的平均数量较基线有显著减少(P <

0.001)。对合并抑郁症和焦虑症患者的亚组分析显示,基于开具抗抑郁药的患者数量显著减少(基线时为68.6%,随访时为56.4%;P = 0.0025)以及开具抗焦虑药的患者数量显著减少(基线时为55.0%,随访时为47.2%;P = 0.037),在真实世界中有显著益处。在基线合并高血压的患者亚组中,fremanezumab治疗使血压有非显著降低。

结论

总体而言,在这项真实世界研究中,偏头痛患者对fremanezumab的依从性和持续性较高,每季度使用fremanezumab的比例更高。持续使用≥6个月的患者急性和预防性偏头痛药物使用显著减少,而基线合并抑郁症和焦虑症的偏头痛患者亚组中,抗抑郁药和抗焦虑药的使用显著减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b85d/9066733/7a2990de6cee/10194_2022_1413_Fig1_HTML.jpg

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