Comprehensive Health Insights, Inc., 325 W. Main St., WFP6W, Louisville, KY 40202.
J Manag Care Spec Pharm. 2014 Jun;20(6):592-600. doi: 10.18553/jmcp.2014.20.6.592.
Varenicline, a nicotinic acetylcholine receptor partial agonist, is a pharmacotherapy indicated for smoking cessation treatment. To date, no research has examined the relationship between out-of-pocket (OOP) expense and varenicline adherence among Medicare beneficiaries.
To (a) characterize medication utilization patterns of varenicline among Medicare members newly initiated on varenicline and (b) examine the relationship between member OOP expense and varenicline medication adherence.
In this retrospective cohort study, pharmacy claims data were used to identify Medicare Advantage Prescription Drug Plan (MAPD) members newly initiated on varenicline. Demographic and clinical characteristics, varenicline medication utilization patterns, and pharmacy costs (total and varenicline-specific) were determined for members included in the study. Varenicline adherence was measured by calculating the proportion of days covered (PDC) over a period of 84 days (12 weeks) after initiation. Multiple regression analysis was used to examine the relationship between varenicline OOP cost and varenicline medication utilization, while controlling for sociodemographic characteristics, clinical factors, and nonvarenicline pharmacy costs.
A total of 15,452 MAPD members were included in the analysis. Mean (SD) subject age was 62.6 (10.0) years; 21.1% (n = 3,256) were dual eligible; and 33.0% (n = 5,106) received a low-income subsidy. Mean (SD) initial varenicline treatment episode duration was 50.8 (37.8) days, with a mean (SD) varenicline days' supply of 47.8 (32.6) obtained by members during the initial treatment episode. Mean (SD) PDC was 0.51 (0.24), and 14.9% (n = 2,302) of members were classified as adherent to treatment (PDC ≥ 0.80). Greater varenicline OOP expense was significantly associated with lower PDC (regression coefficient = -0.058, P less than 0.001) and significantly associated with lower odds of receiving a refill for varenicline (odds ratio 0.594, 95% CI: 0.540-0.655, P less than 0.001).
Among Medicare beneficiaries newly initiated on varenicline, medication adherence was suboptimal, and greater OOP cost was associated with lower adherence and lower odds of refilling varenicline.
伐伦克林是一种烟碱型乙酰胆碱受体部分激动剂,被批准用于戒烟治疗。迄今为止,还没有研究调查医疗保险受益人的自付费用与伐伦克林依从性之间的关系。
(a)描述新接受伐伦克林治疗的医疗保险参保者中伐伦克林的药物使用模式;(b)检验参保者自付费用与伐伦克林药物依从性之间的关系。
本回顾性队列研究使用药房理赔数据,确定了新开始接受伐伦克林治疗的医疗保险优势处方药计划(MAPD)参保者。为纳入研究的参保者确定了人口统计学和临床特征、伐伦克林药物使用模式以及药房费用(总费用和伐伦克林特定费用)。通过计算起始后 84 天(12 周)内的天数占比(PDC)来衡量伐伦克林的依从性。采用多元回归分析,在控制社会人口统计学特征、临床因素和非伐伦克林药房费用的情况下,检验伐伦克林自付费用与伐伦克林药物使用之间的关系。
共纳入 15452 名 MAPD 参保者。受试者平均(标准差)年龄为 62.6(10.0)岁;21.1%(n=3256)为双重资格;33.0%(n=5106)获得了低收入补贴。平均(标准差)初始伐伦克林治疗持续时间为 50.8(37.8)天,参保者在初始治疗期间获得的伐伦克林平均(标准差)供应量为 47.8(32.6)天。平均(标准差)PDC 为 0.51(0.24),14.9%(n=2302)的参保者被归类为治疗依从(PDC≥0.80)。较高的伐伦克林自付费用与较低的 PDC 显著相关(回归系数=-0.058,P<0.001),与获得伐伦克林续药的可能性较低显著相关(比值比 0.594,95%CI:0.540-0.655,P<0.001)。
在新开始接受伐伦克林治疗的医疗保险受益人中,药物依从性并不理想,较高的自付费用与较低的依从性和较低的伐伦克林续药可能性相关。