Laba Tracey-Lea, Jiwani Bashir, Crossland Robert, Mitton Craig
The University of British Columbia, Centre for Clinical Epidemiology and Evaluation, Vancouver, Canada.
The Centre for Health Economics Research and Evaluation, Business School, The University of Technology, Sydney, Australia.
Int J Technol Assess Health Care. 2020 Aug 7:1-6. doi: 10.1017/S0266462320000525.
To describe the implementation of multi-criteria decision analysis (MCDA) into a Canadian public drug reimbursement decision-making process, identifying the aspects of the MCDA approach, and the context that promoted uptake.
Narrative summary of case study describing the how, when, and why of implementing MCDA.
Faced with a fixed budget, a pipeline of expensive but potentially valuable drugs, and potential delays to drug decision making, the Ministry of Health (i.e., decision makers) and its independent expert advisory committee (IAB) sought alternative values-based decision processes. MCDA was considered highly compatible with current processes, but the ability as a stand-alone intervention to address issues of opportunity cost was unclear. The IAB nevertheless collaboratively voted to implement an externally developed MCDA with support from decision makers. After several months of engagement and piloting, implementation was rapid and leveraged strong pre-existing formal and informal communication networks. The IAB as a whole rates new submissions which serves as an input into the deliberative process.
MCDA can be a highly adaptable approach that can be implemented into a functioning drug reimbursement setting when facilitated by (i) a truly limited budget; (ii) a shared vision for change by end-users and decision makers; (iii) using pre-existing deliberative processes; and (iv) viewing the approach as a decision framework rather than the decision (when appropriate). Given the current limitations of MCDA, implementing an academically imperfect tool first and evaluating later reflects a practical solution to real-time fiscal constraints and impending delays to drug approvals that may be faced by decision makers.
描述多标准决策分析(MCDA)在加拿大公共药品报销决策过程中的实施情况,确定MCDA方法的各个方面以及促进其采用的背景。
对描述MCDA实施方式、时间和原因的案例研究进行叙述性总结。
面对固定预算、一系列昂贵但可能有价值的药品以及药品决策可能出现的延误,卫生部(即决策者)及其独立专家咨询委员会(IAB)寻求基于价值的替代决策流程。MCDA被认为与当前流程高度兼容,但作为一种独立干预措施来解决机会成本问题的能力尚不清楚。尽管如此,IAB在决策者的支持下共同投票决定实施外部开发的MCDA。经过几个月的参与和试点,实施过程迅速,并利用了强大的既有正式和非正式沟通网络。IAB对新提交的申请进行整体评分,这为审议过程提供了输入。
MCDA可以是一种高度适应性强的方法,在以下条件的推动下可在有效的药品报销环境中实施:(i)真正有限的预算;(ii)终端用户和决策者对变革的共同愿景;(iii)使用现有的审议流程;(iv)将该方法视为决策框架而非决策本身(在适当的时候)。鉴于MCDA目前的局限性,先实施一个学术上并不完美的工具,之后再进行评估,这反映了一种应对决策者可能面临的实时财政限制和药品审批即将出现的延误的实际解决方案。