Prada Sergio I, Loaiza Johan S
Professor of Economics and Senior Research Associate, Universidad Icesi, Centro PROESA, Calle, Cali, Colombia.
Research Assistant, Universidad Icesi, Centro PROESA.
Am Health Drug Benefits. 2019 Feb;12(1):7-12.
The Medicaid Drug Utilization Review (DUR) program is a 2-phase process conducted by Medicaid state agencies. The first phase is a prospective DUR process and involves electronically monitoring prescription drug claims to identify prescription-related problems, such as therapeutic duplication, contraindications, incorrect dosage, or duration of treatment. The second phase is a retrospective DUR involving ongoing, periodic examinations of claims data to identify patterns of fraud, abuse, underutilization, drug-drug interaction, and medically unnecessary care, and implement corrective actions when needed. The Centers for Medicare & Medicaid Services requires each state to measure the prescription drug cost-savings generated from its DUR programs annually, but it provides no methodology for doing so. An earlier article compared the methodologies used by states to measure cost-savings in their retrospective DUR program in fiscal years 2014 and 2015.
To describe and synthesize the methodologies used by states to measure cost-savings using their Medicaid prospective DUR program in federal fiscal years 2015 and 2016.
For each state, we downloaded from Medicaid's website the cost-savings methodologies included in the Medicaid DUR 2015 and 2016 reports. We then reviewed and synthesized the reports. Methods described by the states were classified into a unique group based on the methodology used, except for Arkansas and Connecticut, which were classified in more than 1 category for the same period.
Currently, 3 different methodologies are being used by states. In 2015 and 2016, the most common methodology used (by 18 states) was the calculation of total claim rejections and subtracting claim resubmissions at the amount actually paid. The comparisons of DUR program cost-savings among states are unreliable, because the states lack a common methodology in the way they measure their performance.
Considering the lack of methodologic consistency among states in measuring the savings in the Medicaid DUR program shown in this analysis, the federal government must lead an effort to define a unique methodology to measure cost-savings in its entire DUR program. This will help to improve the measure of savings among states and understand how this program is performing in that matter.
医疗补助药物使用审查(DUR)计划是由各州医疗补助机构开展的一个分两阶段进行的过程。第一阶段是前瞻性DUR过程,包括对处方药索赔进行电子监控,以识别与处方相关的问题,如治疗重复、禁忌症、剂量不正确或治疗时长不当等。第二阶段是回顾性DUR,包括对索赔数据进行持续、定期审查,以识别欺诈、滥用、利用不足、药物相互作用和医疗上不必要的护理模式,并在需要时采取纠正措施。医疗保险和医疗补助服务中心要求每个州每年衡量其DUR计划所产生的处方药成本节约情况,但未提供这样做的方法。一篇较早的文章比较了各州在2014财年和2015财年衡量其回顾性DUR计划成本节约情况时所使用的方法。
描述并综合各州在2015财年和2016财年使用其医疗补助前瞻性DUR计划衡量成本节约情况时所采用的方法。
对于每个州,我们从医疗补助网站下载了《2015年和2016年医疗补助DUR报告》中包含的成本节约方法。然后我们对这些报告进行了审查和综合。各州描述的方法根据所使用的方法被归入一个独特的类别,但阿肯色州和康涅狄格州在同一时期被归入多个类别。
目前,各州正在使用3种不同的方法。在2015年和2016年,使用最普遍的方法(18个州使用)是计算索赔被拒总数,并减去按实际支付金额重新提交的索赔。各州之间DUR计划成本节约情况的比较不可靠,因为各州在衡量其绩效的方式上缺乏统一的方法。
鉴于本分析显示各州在衡量医疗补助DUR计划节约情况时缺乏方法上的一致性,联邦政府必须牵头努力定义一种独特的方法来衡量其整个DUR计划的成本节约情况。这将有助于改进各州之间节约情况的衡量,并了解该计划在这方面的表现。