Agency for Health Research and Quality (AHRQ) R24 Conference Grant Program (R13)

项目总结 医疗保健研究和质量机构(AHRQ)在以下条件下资助了七个R24 PA-12-114，提议通过制定和传播 为患者、临床医生、政策制定者和医疗保健人员提供循证信息 管理员，回应他们对哪些临床和健康方面的表达需求 系统设计干预对哪些患者在特定情况下最有效 情况。我们的目标是主办一系列以证据为基础的会议 对R24网络开发的信息和工具进行汇总和传播 支持加强学习型医疗体系和学习型医疗 社区模式，以提高卫生保健的结果、质量、可及性和效率 在美国的关爱。会议主题为“让学习医疗系统变得更多” 以病人为中心“体现了我们在集体中分享有效的方法 以患者为中心的研究专业知识的广度和深度：提供相关和 可复制的以患者为中心的循证实践范例 在耐心和利益相关者参与至关重要的情况下，持续分享和学习。 我们的目标是(1)在R24网络的既定势头基础上扩展容量 (2)发展伙伴关系；(2)建立伙伴关系 与利益相关者组织合作，并建设他们参与研究的能力 活动和使用卫生服务研究成果；(3)传播和 落实关于新出现的最佳做法的保健服务研究信息和工具； (4)提高以证据为基础、以患者为中心的意识和参与 由社区参与的研究人员(Cenr)、患者家属咨询委员会进行的研究 (PFAC)，以及其他社区和利益相关者合作伙伴，以使医疗保健更安全， 更高质量、更容易获得、公平和负担得起。 成功的会议成果包括提高对以下问题的认识和理解 通过传播循证结果和以患者为中心的结果研究 提供最佳做法的例子，这有可能改变概念， 成员机构和社区之间的方法和技术；以及 推进循证成果的实施和专门知识。

PROJECT SUMMARY The Agency for Healthcare Research and Quality (AHRQ) funded seven R24s under PA-12-114 that proposed to improve health outcomes by developing and disseminating evidence-based information to patients, clinicians, policy makers, and health care administrators, responding to their expressed needs about which clinical and health system design interventions are most effective for which patients under specific circumstances. Our objective is to host a series of conferences in which evidence-based information and tools developed by the R24 Network are summarized and disseminated to support enhancement of the Learning Healthcare System and Learning Health Care Community models to improve the outcomes, quality, access, and efficiency of health care in America. The conference topic, “Making Learning Healthcare Systems More Patient-Centered,” exemplifies our approach to sharing what works across our collective breadth and depth of patient-centered research expertise: Providing relevant and replicable patient-centered examples of evidence-based practices within a community of continual sharing and learning where patient and stakeholder engagement is essential. We aim to (1) build on the R24 Network's established momentum to extend the capacity of CER and PCOR within a learning health care community; (2) develop partnerships with stakeholder organizations and build their capacity to participate in research activities and use the results of health services research; (3) disseminate and implement health services research information and tools on emerging best practices; and (4) increase the awareness of and involvement in evidence-based, patient-centered research by community-engaged researchers (CEnR), patient family advisory councils (PFAC), and other community and stakeholder partners to make health care safer, higher quality, more accessible, equitable and affordable. Successful conference outcomes include increasing awareness and understanding of patient-centered outcomes research by disseminating evidence-based outcomes and providing examples of best practices, which has the potential to change concepts, methods, and technologies among both member institutions and the community; and advancing implementation and expertise of evidence-based results.