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

项目摘要 医疗保健研究和质量机构（AHRQ）资助了7个R24项目， PA-12-114，建议通过制定和传播 为患者、临床医生、决策者和医疗保健提供循证信息 管理人员，回应他们表达的需要， 系统设计干预措施对特定条件下的患者最有效 情节我们的目标是举办一系列会议， 总结和传播R24网络开发的信息和工具 支持增强学习型医疗保健系统和学习型医疗保健 改善卫生成果、质量、可及性和效率的社区模式 照顾美国。会议的主题是“让学习型医疗保健系统更加 以患者为中心”，阐明了我们在整个团队中分享有效措施的方法 以患者为中心的研究专业知识的广度和深度：提供相关和 社区内可复制的以患者为中心的循证实践示例 在患者和利益相关者的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大容量 在一个学习型卫生保健社区内开展CER和PCOR;（2）发展伙伴关系 与利益攸关方组织合作，并建设其参与研究的能力 （3）开展卫生服务研究活动并利用研究成果; 实施关于新出现的最佳做法的保健服务研究信息和工具; 和（4）提高对以证据为基础，以患者为中心的意识和参与 社区参与研究人员（CEnR）、患者家庭咨询委员会 （PFAC），以及其他社区和利益相关者合作伙伴，使医疗保健更安全， 更高的质量，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方面的认识和理解： 以患者为中心的结果研究，传播基于证据的结果， 提供最佳做法的例子，这些做法有可能改变概念， 方法和技术，并在成员机构和社区之间进行交流;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.