Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
Hospital Pharmacy, Erasmus University Medical Centre, Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.
BioDrugs. 2022 Mar;36(2):217-229. doi: 10.1007/s40259-022-00523-z. Epub 2022 Mar 18.
To encourage the rational prescribing of biologics, payers across Europe have experimented with the implementation of benefit-sharing programs. Benefit-sharing programs are incentive programs that promote the use of 'best-value' off-patent biologics and biosimilars by driving changes in prescribing practices. The aim of these programs is to generate savings that can be shared among stakeholders involved (e.g. health authorities/payers, health care professionals, hospital managers/administration) and are generally used to improve the quality of health care and to increase patients' access to innovative services and medicines. However, the scarcity of information concerning the design, implementation and outcomes of benefit-sharing programs limits the transfer of knowledge to institutions aiming to adopt these types of incentive schemes in the future.
The aim of our study was to map benefit-sharing experiences across Europe, to compare their design and implementation characteristics and to assess the impact of the different benefit-sharing strategies on the use of 'best-value' biologics.
Our approach was based on a literature review and on semi-structured interviews with payers/insurers, regulators, health care professionals and industry representatives.
Our analysis revealed variable design characteristics for benefit-sharing programs, depending on the organization of the health care system, the specific timeframe, the care setting and the policy environment. All these aspects can influence the robustness of benefit-sharing initiatives and their potential to stay in effect over time. We also noted a generalized lack of transparency regarding the distribution of savings and how they are reinvested. This lack of transparency has raised questions on how to optimally implement benefit-sharing in the future.
To realize the full potential of benefit-sharing programs, we identify the importance of (i) setting up and timely monitoring success indicators for these programs; (ii) including quality of care and access to care parameters as success indicators; (iii) establishing clear pathways for the transparent redistribution/reinvestment of savings and (iv) transparently communicating with patients about the outcomes of benefit-sharing programs.
为鼓励合理开具生物制剂处方,欧洲各地的支付方尝试实施了利益共享计划。利益共享计划是一种激励计划,通过推动处方实践的改变,促进使用“最佳价值”非专利生物制剂和生物类似药。这些计划的目的是产生可以在利益相关者(例如卫生当局/支付方、医疗保健专业人员、医院管理人员/行政人员)之间共享的节省,通常用于改善医疗保健质量并增加患者获得创新服务和药物的机会。然而,有关利益共享计划的设计、实施和结果的信息稀缺,限制了向未来希望采用这些激励计划的机构进行知识转移。
我们的研究旨在绘制欧洲各地利益共享的经验,比较其设计和实施特点,并评估不同利益共享策略对“最佳价值”生物制剂使用的影响。
我们的方法基于文献综述和对支付方/保险公司、监管机构、医疗保健专业人员和行业代表的半结构化访谈。
我们的分析显示,利益共享计划的设计特点因医疗保健系统的组织、特定的时间框架、护理环境和政策环境而异。所有这些方面都可能影响利益共享计划的稳健性及其随时间保持有效性的潜力。我们还注意到,关于节省的分配和如何重新投资节省的资金,普遍缺乏透明度。这种缺乏透明度引发了关于如何在未来最佳实施利益共享的问题。
为了充分发挥利益共享计划的潜力,我们确定了以下几点的重要性:(i)为这些计划设定和及时监测成功指标;(ii)将护理质量和获得护理参数纳入成功指标;(iii)为节省的透明再分配/再投资建立明确途径;(iv)与患者透明地沟通利益共享计划的结果。