J Manag Care Spec Pharm. 2019 Apr;25(4):501-506. doi: 10.18553/jmcp.2019.19034. Epub 2019 Mar 21.
Section 3002 of the 21st Century Cures Act, which was signed into law in December 2016, requires the FDA to develop one or more sets of new guidances regarding the collection of patient experience data. To explore how patient-reported outcomes (PROs) can support value-based care and discuss challenges to using PROs more widely, the Academy of Managed Care Pharmacy (AMCP) convened a stakeholder forum in 2017 on PROs and the role they can play in defining the value of health care interventions. This forum achieved consensus on the importance of PROs in improving patient care through implementing value-based payment models and the need for strong organizational systems to fully adopt and use PROs in health care decision making. To explore strategies to build on these findings and implement them in practice, AMCP convened a second forum on October 25, 2018, in Orlando, FL, to focus on identifying specific methods and infrastructure to support the ideal use of PROs in practice. In light of the FDA's plans to propose new guidance for incorporating PROs in the regulatory process, this forum focused on the following: (a) describing the current state of using PROs for FDA regulatory and value-based coverage decisions; (b) defining a process for collecting and sharing PROs with the FDA and managed care organizations for value-based decisions; (c) identifying the necessary infrastructure needed to support the ideal use of PROs; and (d) identifying the health information technology strategies needed to support PRO use across managed care stakeholders. Strategies for the development and implementation of PROs were discussed throughout the forum, including a focus on appropriate activities to address the needs of patients, health care providers, managed care organizations, and life science companies and researchers. Health care leaders representing health plans, integrated delivery systems, pharmacy benefit managers, employers, national associations of health care professionals, patient advocacy organizations, health infrastructure technology companies and biopharmaceutical companies participated in the forum. The AMCP forum was supported in collaboration with Allergan, Amgen, Boehringer Ingelheim, Bristol-Myers Squibb, Merck, Novo Nordisk, PhRMA, Sanofi, Takeda, and Xcenda. DISCLOSURES: The AMCP Partnership Forum and the development of the proceedings document were supported by Allergan, Amgen, Boehringer Ingelheim, Bristol-Myers Squibb, Merck, Novo Nordisk, PhRMA, Sanofi, Takeda, and Xcenda.
《21世纪治愈法案》第3002条于2016年12月签署成为法律,要求美国食品药品监督管理局(FDA)制定一套或多套关于收集患者体验数据的新指南。为探讨患者报告结局(PROs)如何支持基于价值的医疗,并讨论更广泛使用PROs所面临的挑战,管理式医疗药学学会(AMCP)于2017年召开了一次关于PROs及其在界定医疗保健干预措施价值中所起作用的利益相关者论坛。该论坛就PROs通过实施基于价值的支付模式在改善患者护理方面的重要性,以及在医疗保健决策中充分采用和使用PROs所需强大组织系统的必要性达成了共识。为探索基于这些发现的策略并将其付诸实践,AMCP于2018年10月25日在佛罗里达州奥兰多召开了第二次论坛,重点是确定支持在实践中理想使用PROs的具体方法和基础设施。鉴于FDA计划就将PROs纳入监管程序提出新指南,本次论坛聚焦以下方面:(a)描述在FDA监管和基于价值的保险覆盖决策中使用PROs的现状;(b)确定为基于价值的决策收集PROs并与FDA及管理式医疗组织共享的流程;(c)确定支持理想使用PROs所需的必要基础设施;(d)确定支持在管理式医疗利益相关者中使用PROs所需的健康信息技术策略。整个论坛讨论了PROs的开发和实施策略,包括关注满足患者、医疗保健提供者、管理式医疗组织以及生命科学公司和研究人员需求的适当活动。代表健康计划、综合医疗服务系统、药品福利管理机构、雇主、医疗保健专业人员全国协会、患者权益倡导组织、健康基础设施技术公司和生物制药公司的医疗保健领导者参加了此次论坛。AMCP论坛得到了艾尔建、安进、勃林格殷格翰、百时美施贵宝、默克、诺和诺德、美国制药研究与制造商协会、赛诺菲、武田和Xcenda的合作支持。披露:AMCP合作论坛及会议文件的编写得到了艾尔建、安进、勃林格殷格翰、百时美施贵宝、默克、诺和诺德、美国制药研究与制造商协会、赛诺菲、武田和Xcenda的支持。