US Outcomes Research, Merck & Co, Inc, North Wales, Pennsylvania 19454, USA.
Clin Ther. 2009 Nov;31(11):2584-607. doi: 10.1016/j.clinthera.2009.11.030.
The aim of this article was to assess the predictive validity of the Adherence Estimator--a 3-item instrument designed to estimate a patient's propensity to adhere to medications prescribed for chronic disease.
The Adherence Estimator was a 3-item part of a larger survey mailed to adults aged >or=40 years who had a qualifying index prescription filled in June 2008. A qualifying prescription was defined as one for a medication indicated for the treatment of 1 of 5 chronic diseases (cardiovascular disease, dyslipidemia [lipid-lowering drugs], diabetes [oral antihyperglycemics], osteoporosis [oral bisphosphonates], or asthma). Outcomes were compared between the adherence risk groups derived from the Adherence Estimator (low risk = score of 0, medium risk = score of 2-7, and high risk = score of 8-36). Treatment persistence over a period of 9 months was measured using pharmacy claims data. The primary outcome was the median proportion of days covered (PDC) by >or=1 medication during the first 9 months after the index fill. Secondary outcomes included adherence to the index medication, defined as PDC dichotomized to >or=0.80 or <0.80; rate of obtaining a second fill within 30 days of the index fill; and medication possession ratio (MPR) for refill adherence.
There were 1676 usable responses. Ages ranged from 40 to 88 years, with a mean of 64.6 years. Almost two thirds (1076/1676 [64.2%]) of the sample were female, and 1483/1676 (88.5%) were white. Statistically significant associations for all 3 pairwise comparisons (low vs medium risk, low vs high risk, and medium vs high risk) were observed between the Adherence Estimator risk groups for: (1) median PDC (0.655, 0.598, and 0.484 in the low-, medium-, and high-risk groups, respectively [all, false discovery rate [FDR] <0.05]); (2) PDC categorized (293/711 [41.21%], 200/588 [34.01%], and 105/377 [27.85%] [all, FDR <0.05]); and (3) rate of obtaining a second fill for the index medication within 30 days (489/711 [68.78%], 374/588 [63.61%], and 207/377 [54.91%] [all, FDR <0.05]). The low- and high-risk groups differed from one another on: (1) persistence with the index medication at 9 months (265/711 [37.27%] and 95/377 [25.20%]); (2) persistence with >1 medication at 9 months (291/711 [40.93%] and 108/377 [28.65%]); and (3) obtaining a second fill for any medication within 30 days (501/711 [70.46%] and 219/377 [59.09%]) (all, P < 0.05). The low- and high-risk groups differed significantly from one another in MPR for refill adherence (0.912 vs 0.866). Results observed within diseases mirrored those for the total sample, but with less precision.
In the present analysis of the validity of the Adherence Estimator in predicting adherence, baseline propensity to adhere to medications prescribed for chronic diseases was statistically associated with several measures of adherence and persistence, as derived from pharmacy claims data, over a 9-month period.
本文旨在评估 Adherence Estimator 的预测效度,这是一种设计用于估计患者对慢性疾病处方药物的依从性倾向的 3 项工具。
Adherence Estimator 是一项更大的调查的 3 项组成部分,该调查邮寄给年龄大于或等于 40 岁的成年人,这些成年人在 2008 年 6 月有一个合格的索引处方。合格的处方定义为用于治疗 5 种慢性疾病之一(心血管疾病、血脂异常[降脂药物]、糖尿病[口服抗高血糖药物]、骨质疏松症[口服双膦酸盐]或哮喘)的药物之一的处方。通过 Adherence Estimator (低风险=得分 0,中风险=得分 2-7,高风险=得分 8-36)得出的依从风险组之间比较了结果。使用药房索赔数据测量了 9 个月期间的治疗持久性。主要结果是索引填充后前 9 个月内 >或= 1 种药物的天数覆盖率(PDC)的中位数。次要结果包括索引药物的依从性,定义为 PDC 分为 >或= 0.80 或 <0.80;索引填充后 30 天内获得第二次填充的比例;以及再填充依从性的药物占有比(MPR)。
共有 1676 份可使用的回复。年龄范围从 40 岁到 88 岁,平均年龄为 64.6 岁。样本中近三分之二(1076/1676[64.2%])为女性,1483/1676(88.5%)为白人。在所有 3 个两两比较(低风险与中风险、低风险与高风险、中风险与高风险)中,Adherence Estimator 风险组之间观察到了统计学显著关联:(1)中位数 PDC(低风险、中风险和高风险组分别为 0.655、0.598 和 0.484[所有,错误发现率[FDR] <0.05]);(2)PDC 分类(293/711[41.21%]、200/588[34.01%]和 105/377[27.85%] [所有,FDR <0.05]);以及(3)索引药物在 30 天内获得第二次填充的比例(489/711[68.78%]、374/588[63.61%]和 207/377[54.91%] [所有,FDR <0.05])。低风险和高风险组之间在以下方面存在差异:(1)索引药物在 9 个月时的持久性(265/711[37.27%]和 95/377[25.20%]);(2)9 个月时 >1 种药物的持久性(291/711[40.93%]和 108/377[28.65%]);以及(3)在 30 天内获得任何药物的第二次填充(501/711[70.46%]和 219/377[59.09%])(所有,P < 0.05)。低风险和高风险组在再填充依从性的 MPR 方面存在显著差异(0.912 与 0.866)。在疾病内观察到的结果与总样本的结果相似,但准确性较低。
在对 Adherence Estimator 预测依从性的有效性进行的本次分析中,基线对慢性疾病处方药物的依从性倾向与从药房索赔数据中得出的 9 个月期间的几个依从性和持久性指标存在统计学关联。