Elizabeth C S Swart, Jennifer L Nguyen, Samuel K Peasah, Douglas Mager, Urvashi Patel, Chester B Good
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引用次数: 0
Abstract
Background: Chronic diseases such as diabetes are a major burden to the US health care system. High medication adherence helps improve diabetes outcomes and reduce cost. Cost of medications can contribute to nonadherence. Use of a formulary decision support system with e-prescribing may be associated with greater use of generic medications, leading to lower costs and better adherence. A real-time prescription benefit (RTPB) solution provides patient-specific drug pricing, benefit information, and therapeutic options to choose the most cost-effective and clinically appropriate treatment.
Objectives: To examine whether RTPB is associated with increased adherence measured by proportion of days covered, higher utilization of generics, and generic dispensing rate? Is RTPB associated with lower plan and patient out-of-pocket (OOP) per-user per-month costs?
Methods: This study used a retrospective, matched intervention-control analysis of commercial health plan members from a large pharmacy benefits manager. Members were eligible for inclusion if they initiated therapy between January and August 2021. Members were excluded if they were not continuously eligible for coverage over the study period. Members who initiated diabetes therapy with a prescriber using RTPB (intervention) were compared with those new to therapy with a prescriber not using RTPB (control). Index date for both samples was the first medication prescription in the index period. Members were matched on age and sex demographics. The evaluation period lasted 12 months after index date. Multivariable linear regression models were used to assess the impact of an RTPB program on adherence and proportion of prescriptions filled with a generic. A generalized linear model (gamma distribution, log link) estimated plan and OOP patient costs, whereas a generalized linear model model with the Poisson distribution was used to estimate the number of controlling for patient age, sex, social determinants of health score, and other patient- and plan-level covariates.
Results: 1,302 matched pairs were included in the analysis. Findings show the proportion of days covered was 68.7% for control and 71.4% for RTPB members (P < 0.05). The average number of generic prescriptions for control and RTPB samples were 4.06 and 5.66, respectively (P < 0.05) and the generic dispensing rates were 44.9% and 60.1%, respectively (P < 0.05). The mean plan cost per member per month for diabetes medications, for the non-RTPB group, was 32.3% higher than the RTPB sample (a difference of $81.69, P < 0.0001) and the mean patient cost per month was 88.8% higher than the RTPB sample (a difference of $9.71, P < 0.0001).
Conclusions: Access to RTPB tools provides prescribers with formulary benefit and therapeutic options that allow them to provide the lowest-cost clinical treatment, thus improving adherence, increasing use of generic medications, and lowering plan and patient OOP costs.
背景:糖尿病等慢性疾病是美国医疗保健系统的主要负担。高药物依从性有助于改善糖尿病预后并降低成本。药物费用也会导致不依从。在电子处方中使用处方决策支持系统可能与更多地使用非专利药物有关,从而降低成本并提高依从性。实时处方收益(RTPB)解决方案提供针对患者的药物定价、收益信息和治疗方案,以选择最具成本效益和临床合适的治疗方法。目的:研究RTPB是否与增加的依从性(按覆盖天数比例衡量)、更高的仿制药利用率和仿制药配药率相关?RTPB是否与较低的计划和患者每月自付费用(OOP)相关?方法:本研究采用回顾性、配对干预对照分析,对象为一家大型药房福利管理公司的商业健康计划成员。如果会员在2021年1月至8月期间开始治疗,就有资格纳入该计划。如果成员在研究期间不符合连续覆盖资格,则被排除在外。开始使用RTPB治疗的糖尿病患者(干预)与未使用RTPB治疗的新患者(对照)进行比较。两个样本的指标日期均为指标期内的第一次用药处方。成员的年龄和性别进行了匹配。评价期自指标日起12个月。使用多变量线性回归模型来评估RTPB计划对依从性和使用仿制药的处方比例的影响。广义线性模型(伽马分布,对数链接)估计计划和OOP患者成本,而广义线性模型模型与泊松分布用于估计控制患者年龄,性别,健康评分的社会决定因素以及其他患者和计划水平协变量的数量。结果:共纳入1302对配对。结果显示,对照组的覆盖天数比例为68.7%,RTPB成员的覆盖天数比例为71.4% (P P P P P P)结论:使用RTPB工具为处方医师提供了处方效益和治疗选择,使他们能够提供最低成本的临床治疗,从而提高依从性,增加仿制药的使用,降低计划和患者的OOP成本。
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.