Associate Professor, Center for Pharmaceutical Economics, College of Pharmacy, University of Arizona, Tucson.
Assistant Professor, Department of Pharmacy & Health Services, University of Washington, Seattle.
J Manag Care Spec Pharm. 2020 Jun;26(6):689-695. doi: 10.18553/jmcp.2020.26.6.689.
To propose a set of guidelines for use by health care organizations in the United States that seek useful, comparative clinical information and economic analysis on pharmaceutical products to make sound drug purchasing decisions.
Based on a therapy intervention approach, the guidelines provide a structured framework to help managed care purchasers become more consistent in how they evaluate drug products for inclusion in the formulary. The guidelines factor in the need to examine the impact of new drug products on overall costs within the entire health system.
Intended for use by managed care organizations in the U.S. that purchase prescription drugs.
Not applicable.
Not applicable.
The guidelines provide MCOs with a new systematic approach for identifying the overall cost and clinical outcomes impact of drug therapies. The guidelines are designed to take into account the characteristics of the patient population being treated and the fact that patients generally are redistributed among different treatment categories once a new drug product is introduced, thus offering MCOs an analysis model that extends beyond the traditional partial cost-outcomes approach. Emphasis is placed on looking at the cost-outomes impact of a new drug or therapy within a systems or disease area framework in which the redistribution of patients between therapy options is explicitly modelled. The guidelines specify that the following information elements be used in pharmacoeonomic analysis: product description, place in therapy, comparator products, therapy intervention framework, supporting clinical data, supporting pharmacoeconomic data, system impact assessments-costs-outcomes, overall assessment, and bibliography and supporting materials.
为美国的医疗保健组织提出一套指导方针,以获取有关药品的有用的、可比的临床信息和经济分析,从而做出明智的药品采购决策。
基于治疗干预方法,这些指南提供了一个结构化的框架,帮助管理式医疗购买者在评估纳入处方集的药品产品时更加一致。这些指南考虑了需要检查新药产品对整个医疗体系总成本的影响。
供美国购买处方药品的管理式医疗组织使用。
不适用。
不适用。
这些指南为 MCO 提供了一种新的系统方法,用于确定药物治疗的总体成本和临床结果的影响。这些指南旨在考虑所治疗患者人群的特征,以及一旦引入新的药品产品,患者通常会在不同的治疗类别之间重新分配的事实,从而为 MCO 提供了一种分析模型,该模型超越了传统的部分成本-结果方法。重点是在系统或疾病领域框架内查看新药或疗法的成本-结果影响,其中明确对患者在治疗方案之间的重新分配进行建模。这些指南规定,药物经济学分析应使用以下信息要素:产品描述、治疗中的位置、比较产品、治疗干预框架、支持临床数据、支持药物经济学数据、系统影响评估-成本-结果、总体评估以及参考资料和支持材料。