Pharmaceutical Outcomes Research & Policy Program, Department of Pharmacy, University of Washington, Seattle, WA 98195, USA.
Value Health. 2013 Jul-Aug;16(5):703-19. doi: 10.1016/j.jval.2013.04.011. Epub 2013 Jul 19.
There is a significant and growing interest among both payers and producers of medical products for agreements that involve a "pay-for-performance" or "risk-sharing" element. These payment schemes-called "performance-based risk-sharing arrangements" (PBRSAs)-involve a plan by which the performance of the product is tracked in a defined patient population over a specified period of time and the amount or level of reimbursement is based on the health and cost outcomes achieved. There has always been considerable uncertainty at product launch about the ultimate real-world clinical and economic performance of new products, but this appears to have increased in recent years. PBRSAs represent one mechanism for reducing this uncertainty through greater investment in evidence collection while a technology is used within a health care system. The objective of this Task Force report was to set out the standards that should be applied to "good practices"-both research and operational-in the use of a PBRSA, encompassing questions around the desirability, design, implementation, and evaluation of such an arrangement. This report provides practical recommendations for the development and application of state-of-the-art methods to be used when considering, using, or reviewing PBRSAs. Key findings and recommendations include the following. Additional evidence collection is costly, and there are numerous barriers to establishing viable and cost-effective PBRSAs: negotiation, monitoring, and evaluation costs can be substantial. For good research practice in PBRSAs, it is critical to match the appropriate study and research design to the uncertainties being addressed. Good governance processes are also essential. The information generated as part of PBRSAs has public good aspects, bringing ethical and professional obligations, which need to be considered from a policy perspective. The societal desirability of a particular PBRSA is fundamentally an issue as to whether the cost of additional data collection is justified by the benefits of improved resource allocation decisions afforded by the additional evidence generated and the accompanying reduction in uncertainty. The ex post evaluation of a PBRSA should, however, be a multidimensional exercise that assesses many aspects, including not only the impact on long-term cost-effectiveness and whether appropriate evidence was generated but also process indicators, such as whether and how the evidence was used in coverage or reimbursement decisions, whether budget and time were appropriate, and whether the governance arrangements worked well. There is an important gap in the literature of structured ex post evaluation of PBRSAs. As an innovation in and of themselves, PBRSAs should also be evaluated from a long-run societal perspective in terms of their impact on dynamic efficiency (eliciting the optimal amount of innovation).
支付方和医疗产品生产者都对涉及“按效付费”或“风险共担”要素的协议表现出浓厚的兴趣。这些支付计划被称为“基于绩效的风险共担安排”(PBRSAs),涉及一项计划,根据该计划,在特定时间段内,在特定患者群体中跟踪产品的表现,报销金额或水平基于所取得的健康和成本结果。新产品在推出时,其最终的实际临床和经济表现存在相当大的不确定性,但近年来这种不确定性似乎有所增加。通过在技术在医疗保健系统中使用的同时,投入更多的证据收集,PBRSAs 代表了一种降低这种不确定性的机制。本报告的目的是制定应适用于“良好实践”的标准,包括在使用 PBRSA 时围绕此类安排的可取性、设计、实施和评估的研究和运营问题。本报告为开发和应用最先进的方法提供了实用建议,以供在考虑、使用或审查 PBRSAs 时使用。主要发现和建议包括以下内容。额外的证据收集成本高昂,并且建立可行且具有成本效益的 PBRSAs 存在诸多障碍:谈判、监测和评估成本可能相当高。对于 PBRSAs 中的良好研究实践,将适当的研究和研究设计与正在解决的不确定性相匹配至关重要。良好的治理流程也是必不可少的。作为 PBRSAs 一部分生成的信息具有公共利益方面,带来了道德和专业义务,需要从政策角度进行考虑。特定 PBRSA 的社会可取性从根本上说是一个问题,即是否值得通过生成的额外证据和随之而来的不确定性降低来提高资源分配决策的改善来证明额外数据收集的成本是合理的。然而,PBRSA 的事后评估应该是一个多维的评估,评估许多方面,包括不仅对长期成本效益的影响,而且对是否生成了适当的证据,还包括过程指标,例如证据是否以及如何用于覆盖范围或报销决策,是否适当预算和时间,以及治理安排是否运作良好。在 PBRSAs 的事后结构化评估文献中存在一个重要的差距。作为一种创新,从长期的社会角度来看,PBRSAs 还应该根据其对动态效率的影响进行评估(引出最佳创新量)。