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Patient participation in ERS guidelines and research projects: the EMBARC experience

机译:患者参与ERS指南和研究项目:EMBARC的经验

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pThe European Multicentre Bronchiectasis Audit and Research Collaboration (EMBARC) is a European Respiratory Society (ERS) Clinical Research Collaboration dedicated to improving research and clinical care for people with bronchiectasis. EMBARC has created a European Bronchiectasis Registry, funded by the ERS and by the European Union (EU) Innovative Medicines Initiative Programme./ppFrom the outset, EMBARC had the ambition to be a patient-focussed project. In contrast to many respiratory diseases, however, there are no specific patient charities or European patient organisations for patients with bronchiectasis and no existing infrastructure for patient engagement. This article describes the experience of EMBARC and the European Lung Foundation in establishing a patient advisory group and then engaging this group in European guidelines, an international registry and a series of research studies./ppPatient involvement in research, clinical guidelines and educational activities is increasingly advocated and increasingly important. Genuine patient engagement can achieve a number of goals that are critical to the success of an EU project, including focussing activities on patient priorities, allowing patients to direct the clinical and research agenda, and dissemination of guidelines and research findings to patients and the general public. Here, we review lessons learned and provide guidance for future ERS task forces, EU-funded projects or clinical research collaborations that are considering patient involvement./ph3Educational aims/h3pTo understand the different ways in which patients can contribute to clinical guidelines, research projects and educational activities./ppTo understand the barriers and potential solutions to these barriers from a physician’s perspective, in order to ensure meaningful patient involvement in clinical projects./ppTo understand the barriers and potential solutions from a patient’s perspective, in order to meaningfully involve patients in clinical projects./p
机译:>欧洲多中心支气管扩张审核与研究合作组织(EMBARC)是欧洲呼吸学会(ERS)临床研究合作组织,致力于改善支气管扩张患者的研究和临床护理。 EMBARC建立了欧洲支气管扩张注册机构,由ERS和欧洲联盟(EU)创新药物倡议计划资助。 >从一开始,EMBARC就有志于成为一个以患者为中心的项目。但是,与许多呼吸系统疾病相反,没有针对支气管扩张患者的特定患者慈善机构或欧洲患者组织,也没有现有的患者参与基础设施。本文介绍了EMBARC和欧洲肺基金会在建立患者咨询小组,然后使该小组参与欧洲指南,国际注册管理机构和一系列研究研究方面的经验。 >患者参与研究,临床准则和教育活动越来越受到拥护和重视。真正的患者参与可以实现对欧盟项目成功至关重要的许多目标,包括将活动重点放在患者的优先事项上,允许患者指导临床和研究议程,以及向患者和公众传播指导方针和研究结果。在这里,我们将总结经验教训,并为将来的ERS工作组,欧盟资助的项目或正在考虑患者参与的临床研究合作提供指导。 >教育目标 >了解不同的方式其中的患者可以为临床指南,研究项目和教育活动做出贡献。 >从医师的角度了解障碍以及这些障碍的潜在解决方案,以确保有意义的患者参与临床项目。 > p> >从患者的角度了解障碍和潜在的解决方案,以使患者有意义地参与临床项目。

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