Curkendall S, Patel V, Gleeson M, Campbell R S, Zagari M, Dubois R
Cerner LifeSciences, Beverly Hills, California, USA.
Arthritis Rheum. 2008 Oct 15;59(10):1519-26. doi: 10.1002/art.24114.
To assess the impact of patient out-of-pocket (OOP) expenditures on adherence and persistence with biologics in patients with rheumatoid arthritis (RA).
An inception cohort of RA patients with pharmacy claims for etanercept or adalimumab during 2002-2004 was selected from an insurance claims database of self-insured employer health plans (n=2,285) in the US. Adherence was defined as medication possession ratio (MPR): the proportion of the 365 followup days covered by days supply. Persistence was determined using a survival analysis of therapy discontinuation during followup. Patient OOP cost was measured as the patient's coinsurance and copayments per week of therapy, and as the proportion of the total medication charges paid by the patient. Multivariate linear regression models of MPR and proportional hazards models of persistence were used to estimate the impact of cost, adjusting for insurance type and demographic and clinical variables.
Mean +/- SD OOP expenditures averaged $7.84+/-$14.15 per week. Most patients (92%) paid less than $20 OOP for therapy/week. The mean +/- SD MPR was 0.52+/-0.31. Adherence significantly decreased with increased weekly OOP (coeff= -0.0035, P<0.0001) and with a higher proportion of therapy costs paid by patients (coeff= -0.8794, P<0.0001), translating into approximately 1 week of therapy lost per $5.50 increase in weekly OOP. Patients whose weekly cost exceeded $50 were more likely to discontinue than patients with lower costs (hazard ratio 1.58, P<0.001).
Most patients pay less than $20/week for biologics, but a small number have high OOP expenses, associated with lower medication compliance. The adverse impact of high OOP costs on adherence, persistence, and outcomes must be considered when making decisions about increasing copayments.
评估类风湿关节炎(RA)患者的自付费用(OOP)对生物制剂治疗依从性和持续性的影响。
从美国自保雇主健康计划的保险理赔数据库中选取2002年至2004年期间有依那西普或阿达木单抗药房理赔记录的RA患者起始队列(n = 2285)。依从性定义为药物持有率(MPR):即365天随访期内按日供应量计算的覆盖天数比例。持续性通过随访期间治疗中断的生存分析来确定。患者的OOP成本以患者每周的共保费用和自付费用来衡量,也以患者支付的总药物费用比例来衡量。使用MPR的多元线性回归模型和持续性的比例风险模型来估计成本的影响,并对保险类型、人口统计学和临床变量进行调整。
平均±标准差的OOP支出平均为每周7.84美元±14.15美元。大多数患者(92%)每周的治疗OOP费用低于20美元。平均±标准差的MPR为0.52±0.31。随着每周OOP的增加,依从性显著降低(系数 = -0.0035,P < 0.0001),并且随着患者支付的治疗费用比例增加,依从性也显著降低(系数 = -0.8794,P < 0.0001),这意味着每周OOP每增加5.50美元,大约会损失1周的治疗时间。每周费用超过50美元的患者比费用较低的患者更有可能停药(风险比1.58,P < 0.001)。
大多数患者每周支付生物制剂的费用低于20美元,但少数患者有较高的OOP费用,这与较低的药物依从性相关。在做出增加自付费用的决策时,必须考虑高OOP成本对依从性、持续性和治疗结果的不利影响。