Groningen University, Groningen Research Institute of Pharmacy, Groningen, The Netherlands.
National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands.
Pharmacoeconomics. 2022 Mar;40(3):241-248. doi: 10.1007/s40273-021-01110-w. Epub 2021 Dec 16.
Health care decision makers in many jurisdictions use cost-effectiveness analysis based on health economic decision models for policy decisions regarding coverage and price negotiation for medicines and medical devices. While validation of health economic decision models has always been considered important, many reviews of model-based cost-effectiveness studies report limitations regarding their validation. The current opinion paper discusses four aspects of current health economic decision modeling with relevance for future directions in model validation: increased use of complex models, international cooperation, open-source modeling, and stakeholder involvement. First, new, more complex clinical study designs and treatment strategies may require relatively complex model structures and/or input data analyses. Simultaneously, more widespread technical knowledge along with wider data availability have led to a broader range of model types. This puts extra requirements on model validation and transparency. Second, increased international cooperation of policy makers and, in particular, health technology assessment (HTA) authorities in performing model assessments is discussed in relation to the repeated use of health economic models (multi-use disease models). We argue such coordinated efforts may benefit model validity. Third, open-source modeling is discussed as one possible answer to increased transparency requirements. Finally, involvement of all relevant stakeholders throughout the whole decision process is an ongoing development that necessarily also includes health economic modeling. We argue this implies that model validity should be considered in a broader perspective, with more focus on conceptual modeling, model transparency, accuracy requirements, and choice of relevant model outcomes than previously.
许多司法管辖区的医疗保健决策制定者使用基于健康经济决策模型的成本效益分析来制定有关药品和医疗器械覆盖范围和价格谈判的政策决策。虽然验证健康经济决策模型一直被认为很重要,但许多基于模型的成本效益研究的审查报告都指出了其验证方面的局限性。本观点文章讨论了当前健康经济决策建模的四个方面,这些方面对于模型验证的未来方向具有重要意义:更多地使用复杂模型、国际合作、开源建模和利益相关者的参与。首先,新的、更复杂的临床研究设计和治疗策略可能需要相对复杂的模型结构和/或输入数据分析。同时,随着技术知识的普及和数据可用性的增加,模型类型也更加多样化。这对模型验证和透明度提出了额外的要求。其次,讨论了决策者,特别是卫生技术评估(HTA)机构在进行模型评估方面增加国际合作的问题,这与重复使用健康经济模型(多用途疾病模型)有关。我们认为,这种协调一致的努力可能会使模型的有效性受益。第三,讨论了开源建模作为增加透明度要求的一种可能解决方案。最后,在整个决策过程中让所有相关利益相关者参与是一个持续的发展,这必然也包括健康经济建模。我们认为,这意味着应该从更广泛的角度考虑模型的有效性,而不仅仅是关注概念建模、模型透明度、准确性要求和选择相关的模型结果,这比以往任何时候都更加重要。