Paolino Andrea R, McGlynn Elizabeth A, Lieu Tracy, Nelson Andrew F, Prausnitz Stephanie, Horberg Michael A, Arterburn David E, Gould Michael K, Laws Reesa L, Steiner John F
Kaiser Permanente Colorado.
Kaiser Permanente Southern California.
EGEMS (Wash DC). 2016 Mar 28;4(2):1216. doi: 10.13063/2327-9214.1216. eCollection 2016.
The Patient Outcomes Research to Advance Learning (PORTAL) Network was established with funding from the Patient-Centered Outcomes Research Institute (PCORI) in 2014. The PORTAL team adapted governance structures and processes from past research network collaborations. We will review and outline the structures and processes of the PORTAL governance approach and describe how proactively focusing on priority areas helped us to facilitate an ambitious research agenda.
For years a variety of funders have supported large-scale infrastructure grants to promote the use of clinical datasets to answer important comparative effectiveness research (CER) questions. These awards have provided the impetus for health care systems to join forces in creating clinical data research networks. Often, these scientific networks do not develop governance processes proactively or systematically, and address issues only as problems arise. Even if network leaders and collaborators foresee the need to develop governance approaches, they may underestimate the time and effort required to develop sound processes. The resulting delays can impede research progress.
Because the PORTAL sites had built trust and a foundation of collaboration by participating with one another in past research networks, essential elements of effective governance such as guiding principles, decision making processes, project governance, data governance, and stakeholders in governance were familiar to PORTAL investigators. This trust and familiarity enabled the network to rapidly prioritize areas that required sound governance approaches: responding to new research opportunities, creating a culture of trust and collaboration, conducting individual studies, within the broader network, assigning responsibility and credit to scientific investigators, sharing data while protecting privacy/security, and allocating resources. The PORTAL Governance Document, complete with a Toolkit of Appendices is included for reference and for adaptation by other networks.
As a result of identifying project-based governance priorities (IRB approval, subcontracting, selection of new research including lead PI and participating sites, and authorship) and data governance priorities (reciprocal data use agreement, analytic plan procedures, and other tools for data governance), PORTAL established most of its governance structure by Month 6 of the 18 month project. This allowed science to progress and collaborators to experience first-hand how the structures and procedures functioned in the remaining 12 months of the project, leaving ample time to refine them and to develop new structures or processes as necessary.
The use of procedures and processes with which participating investigators and their home institutions were already familiar allowed project and regulatory requirements to be established quickly to protect patients, their data, and the health care systems that act as stewards for both. As the project progressed, PORTAL was able to test and adjust the structures it put place, and to make substantive revisions by Month 17. As a result, priority processes have been predictable, transparent and effective.
CONCLUSION/NEXT STEPS: Strong governance practices are a stewardship responsibility of research networks to justify the trust of patients, health plan members, health care delivery organizations, and other stakeholders. Well-planned governance can reduce the time necessary to initiate the scientific activities of a network, a particular concern when the time frame to complete research is short. Effective network and data governance structures protect patient and institutional data as well as the interests of investigators and their institutions, and assures that the network has built an environment to meet the goals of the research.
患者结局研究促进学习(PORTAL)网络于2014年在患者为中心的结局研究机构(PCORI)的资助下成立。PORTAL团队借鉴了以往研究网络合作中的治理结构和流程。我们将回顾并概述PORTAL治理方法的结构和流程,并描述积极关注优先领域如何帮助我们推动一项雄心勃勃的研究议程。
多年来,各种资助者支持大规模基础设施拨款,以促进利用临床数据集来回答重要的比较效果研究(CER)问题。这些奖项推动了医疗保健系统联合起来创建临床数据研究网络。通常,这些科学网络不会主动或系统地制定治理流程,只是在问题出现时才加以解决。即使网络领导人和合作者预见到需要制定治理方法,他们可能也会低估制定完善流程所需的时间和精力。由此导致的延迟可能会阻碍研究进展。
由于PORTAL各站点通过以往参与研究网络彼此建立了信任和合作基础,PORTAL研究人员熟悉有效治理的基本要素,如指导原则、决策过程、项目治理、数据治理以及治理中的利益相关者。这种信任和熟悉使该网络能够迅速确定需要完善治理方法的领域:应对新的研究机会、营造信任与合作的文化、在更广泛的网络内开展个体研究、向科学研究人员分配责任和荣誉、在保护隐私/安全的同时共享数据以及分配资源。PORTAL治理文件及其附录工具包可供参考,其他网络也可进行改编。
通过确定基于项目的治理优先事项(机构审查委员会批准、分包、选择新研究包括首席研究员和参与站点以及作者身份)和数据治理优先事项(互惠数据使用协议、分析计划程序以及其他数据治理工具),PORTAL在18个月项目的第6个月时就建立了大部分治理结构。这使得科学研究能够推进,合作者能够在项目剩余的12个月里亲身体验这些结构和程序的运作方式,从而有足够的时间对其进行完善,并在必要时开发新的结构或流程。
使用参与研究的人员及其所在机构已经熟悉的程序和流程,使得能够迅速确立项目和监管要求,以保护患者、他们的数据以及作为两者管理者的医疗保健系统。随着项目的推进,PORTAL能够测试和调整其建立的结构,并在第17个月时进行实质性修订。因此,优先流程具有可预测性、透明度和有效性。
结论/下一步措施:强有力的治理实践是研究网络的管理责任,以证明患者、健康计划成员、医疗保健服务组织和其他利益相关者的信任是合理的。精心规划的治理可以减少启动网络科学活动所需的时间,在完成研究的时间框架较短时,这是一个特别需要关注的问题。有效的网络和数据治理结构保护患者和机构数据以及研究人员及其机构的利益,并确保网络营造了一个实现研究目标的环境。