酒精相关肝病多方利益相关者中心(ARMS-Hub),以加强英国服务不足社区的研究活动

Ashwin D Dhanda, V. Allgar, Neeraj Bhala, Lynne Callaghan, Joana Castro, Shilpa Chokshi, Amanda Clements, Wendy Clyne, Colin Drummond, Ewan Forrest, Lesley Manning, Richard Parker, Debbie Shawcross, Jennifer Towey
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引用次数: 0

摘要

背景 在英国,酗酒是导致死亡和残疾的第三大风险因素,英国国家医疗服务体系(NHS)每年因此花费 35 亿英镑。尽管酒精相关肝病(ArLD)的发病率很高,给医疗保健带来了沉重负担,但针对其预防、发病率和死亡率的研究却少之又少。究其原因,包括耻辱感以及公共、慈善和商业资助机构缺乏兴趣。该项目的目标是确定和发展跨学科合作伙伴关系,探讨 ArLD 的耻辱化问题,建立一个具有代表性的患者和公众参与小组 (PPIE),提高研究能力,并针对关键的研究重点制定跨学科研究计划。方法 ArLD 网络由项目指导小组成员确定。邀请不同背景的医疗保健专业人员(HCP)加入 ARMS-Hub。通过慈善机构和支持团体邀请 PPIE 代表。对研究领域进行确定、讨论、优先排序和排序。在一次面对面的研讨会上对研究问题进行了完善。制定了一项导师计划,以鼓励和促进早期职业研究人员建立联系和进行知识交流。结果 我们与 31 名高级保健人员和 40 名 PPIE 成员一起建立了 ARMS 枢纽。共召开了五次利益相关者会议,其中包括 PPIE 代表。举行了三次虚拟会议和三次现场 PPIE 会议。会议期间确定的与 ARLD 耻辱化相关的主题包括教育和认识、语言和获取。会议确定的优先事项包括:心理健康和肝脏服务之间的脱节、围绕酒精的广泛危害开展的教育,以及对保健从业人员开展的有关污名化的教育。我们建立了一个导师网络,定期举行会议,以支持新研究想法的开发。结论 耻辱感是专业人士和 PPIE 缺乏研究参与的核心原因。已确定的主要优先事项与心理健康和肝脏服务之间的脱节有关。通过这项合作研究,我们制定了一项研究议程,以解决这一首要问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An alcohol-related liver disease multi-stakeholder hub (ARMS-Hub) to enhance research activity in underserved communities in the UK
Background Alcohol use is the third leading risk factor of death and disability in the UK and costs the NHS £3.5 billion per year. Despite the high prevalence and healthcare burden of Alcohol-related Liver Disease (ArLD), there has been minimal research addressing prevention, morbidity and mortality. Reasons for this include stigma and lack of interest from public, charitable and commercial funding bodies. The objectives of this project were to identify and develop interdisciplinary partnerships, to explore stigma in ArLD, to develop a representative Patient and Public Involvement and Engagement (PPIE) group, to build research capacity, and to develop interdisciplinary research proposals targeting key research priorities. Methods ArLD networks were identified by members of the Project Steering Group. Health Care Professionals (HCPs) from different backgrounds were invited to join the ARMS-Hub. PPIE representatives were invited through charities and support groups. Research areas were identified, discussed, prioritised and ranked. Research questions were refined during an in-person symposium. A mentorship programme was created to encourage and facilitate networking and knowledge exchange for early career researchers. Results We established the ARMS-Hub with 31 HCPs and 40 PPIE members. There were five stakeholder meetings, which included PPIE representation. Three virtual and three in-person PPIE meetings took place. Topics relevant to stigma in ARLD identified during the meetings were education and awareness, language, and access. Priorities identified were the disconnect between mental health and liver services, education around the wider harms of alcohol, and education of HCPs regarding stigma. We established a mentorship network that regularly meets to support development of new research ideas. Conclusions Stigma is central to lack of research engagement from professionals and PPIE. The main priority identified relates to the disconnect between mental health and liver services. This collaborative study has allowed development of a research agenda to address this priority.
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