自注射降钙素基因相关肽单克隆抗体的偏头痛患者在12个月内的医疗资源利用和直接成本:一项美国真实世界的研究

IF 2.3 4区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Oralee J Varnado, Brenna Brady, Anthony Zagar, Yvonne Robles, Alan Ó Céilleachair, Margaret Hoyt
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引用次数: 0

摘要

背景:降钙素基因相关肽单克隆抗体(CGRP mab)已被批准用于偏头痛预防。与启动不同CGRP单克隆抗体相关的卫生保健资源利用率(HCRU)和直接成本的比较信息有限。目的:比较美国偏头痛患者自注射CGRP单克隆抗体、galcanezumab、fremanezumab或erenumab的全因和偏头痛相关HCRU和直接成本。方法:这项回顾性队列研究使用了来自Merative Marketscan商业和医疗保险数据库的数据。在2018年5月至2020年9月(指数期)期间,对上述CGRP单克隆抗体至少有一次索赔(首次索赔=指数)的成年人,在指数前(基线[BL])和指数后(随访[FU])连续入组12个月。排除BL期间要求使用指标药物的患者。平均HCRU和平均总费用(住院、门诊和门诊药房费用)在指数后12个月内进行评估。倾向评分匹配用于平衡galcanezumab与fremanezumab(2:1)和galcanezumab与erenumab(1:1)队列。结果的P值:匹配后,galcanezumab与fremanezumab (n= 2674组)和galcanezumab与erenumab (n= 3503组)队列的患者人口统计学和临床特征相似。相对于BL,在指数后的12个月期间,所有队列中观察到全因和偏头痛相关的HCRU(住院和门诊就诊)数值较低,而门诊药房的HCRU数值较高。在所有队列中,全因和偏头痛相关的总成本(平均)在FU期间均较高(所有P=0.825]和467美元对468美元[P=0.990]), galcanezumab与erenumab(504美元对499美元[P=0.934]和462美元对443美元[P=0.375])。门诊药房费用在偏头痛相关费用中占很大比例,而全因费用在很大程度上受门诊费用的驱动。结论:在使用galcanezumab、fremanezumab和erenumab治疗的患者中,自注射CGRP单克隆抗体预防偏头痛12个月后观察到的HCRU和直接成本差异在数值上相似。应该做更多的工作来了解这些药物在其他重要因素方面是否有不同的表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Health care resource utilization and direct costs incurred over 12 months by patients with migraine initiating self-injectable calcitonin gene-related peptide monoclonal antibodies: A US real-world study.

Background: Calcitonin gene-related peptide monoclonal antibodies (CGRP mAbs) are approved for migraine prevention. Limited information is available comparing the health care resource utilization (HCRU) and direct costs associated with initiating different CGRP mAbs.

Objective: To compare all-cause and migraine-related HCRU and direct costs in US patients with migraine initiating the self-injectable CGRP mAbs, galcanezumab, fremanezumab, or erenumab.

Methods: This retrospective cohort study used data from Merative Marketscan Commercial and Medicare Databases. Adults with at least 1 claim (first claim=index) for the above CGRP mAbs between May 2018 and September 2020 (index period), with continuous enrollment for 12 months pre-index (baseline [BL]) and post-index (follow-up [FU]) were included. Patients with a claim for index drug during BL were excluded. Mean HCRU and mean total costs (inpatient, outpatient, and outpatient pharmacy costs) were evaluated over 12 months post-index. Propensity score matching was used to balance the galcanezumab vs fremanezumab (2:1) and galcanezumab vs erenumab (1:1) cohorts. P values of <0.05 were considered statistically significant.

Results: After matching, patient demographics and clinical characteristics were similar between galcanezumab vs fremanezumab (n=2,674 sets) and galcanezumab vs erenumab (n=3,503 sets) cohorts. Relative to BL, numerically lower all-cause and migraine-related HCRU (inpatient and outpatient visits) were observed in all cohorts over the 12-month post-index period, whereas outpatient pharmacy HCRU was numerically higher. All-cause and migraine-related total costs (mean) were higher over the FU period in all cohorts (all P < 0.001). Mean all-cause and migraine-related cost increases were numerically similar for galcanezumab vs fremanezumab ($503 vs $518 [P=0.825] and $467 vs $468 [P=0.990]), and for galcanezumab vs erenumab ($504 vs $499 [P=0.934] and $462 vs $443 [P=0.375]). Outpatient pharmacy costs contributed greatly to migraine-related costs, whereas all-cause costs were greatly driven by outpatient costs.

Conclusions: HCRU and direct cost differences observed at 12 months following initiation of self-injectable CGRP mAbs for migraine prevention were numerically similar across cohorts for patients treated with galcanezumab, fremanezumab, and erenumab. More work should be done to learn if these drugs perform differently with respect to other important factors not examined here.

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来源期刊
Journal of managed care & specialty pharmacy
Journal of managed care & specialty pharmacy Health Professions-Pharmacy
CiteScore
3.50
自引率
4.80%
发文量
131
期刊介绍: JMCP welcomes research studies conducted outside of the United States that are relevant to our readership. Our audience is primarily concerned with designing policies of formulary coverage, health benefit design, and pharmaceutical programs that are based on evidence from large populations of people. Studies of pharmacist interventions conducted outside the United States that have already been extensively studied within the United States and studies of small sample sizes in non-managed care environments outside of the United States (e.g., hospitals or community pharmacies) are generally of low interest to our readership. However, studies of health outcomes and costs assessed in large populations that provide evidence for formulary coverage, health benefit design, and pharmaceutical programs are of high interest to JMCP’s readership.
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