Sheldon Elena, Ezaydi Naseeb, Ditmore Melanie, Fuseini Olga, Ainley Rachel, Robinson Kerry, Hind Daniel, Lobo Alan J
Sheffield Centre for Health and Related Research (ScHARR), The University of Sheffield, Sheffield, UK.
VoiceAbility, London, UK.
Health Expect. 2024 Apr;27(2):e14004. doi: 10.1111/hex.14004.
Involving people with lived experience is fundamental to healthcare development and delivery. This is especially true for inflammatory bowel disease (IBD) services, where holistic and personalised models of care are becoming increasingly important. There is, however, a significant lack of representation of underserved and diverse groups in IBD research, and there are significant barriers to healthcare access and utilisation among minority groups in IBD. IBD centres need to be aware of these experiences to address barriers via service changes, improve interactions with local communities and promote meaningful engagement for improved health outcomes.
A pragmatic community-based approach was taken to engage with leaders and members of underserved groups across 11 workshops representing Roma, Afro-Caribbean, people of African descent and the wider black, Asian and minority ethnic (BAME) communities, Muslim women, refugee community members, deprived areas of South Yorkshire, LGBTQ+ and deaf populations. Thematic analysis of field notes identified patterns of attention across the community groups and where improvements to services were most frequently suggested.
Findings demonstrated several barriers experienced to healthcare access and utilisation, including language accessibility, staff attitudes and awareness, mental health and stigma, continuity of support, and practical factors such as ease of service use and safe spaces. These barriers acted as a lever to co-producing service changes that are responsive to the health and social care needs of these groups.
Engaging with people from a range of communities is imperative for ensuring that service improvements in IBD are accessible and representative of individual needs and values.
Local community leaders and members of community groups actively participated in the co-design and development of improvements to the IBD service for a local hospital. Their contributions further informed a pilot process for quality improvement programmes in IBD centres.
让有实际生活经验的人参与其中是医疗保健发展与提供的基础。对于炎症性肠病(IBD)服务而言尤其如此,在该领域,整体化和个性化的护理模式正变得越来越重要。然而,在IBD研究中,服务不足和多样化群体的代表性严重不足,并且IBD中的少数群体在医疗保健获取和利用方面存在重大障碍。IBD中心需要了解这些经历,以便通过改变服务来消除障碍,改善与当地社区的互动,并促进有意义的参与以改善健康结果。
采用务实的基于社区的方法,通过11个研讨会与服务不足群体的领导者和成员进行接触,这些群体包括罗姆人、非裔加勒比人、非洲裔人士以及更广泛的黑、亚和少数族裔(BAME)社区、穆斯林女性、难民社区成员、南约克郡的贫困地区、LGBTQ+群体和聋人群体。对实地记录进行主题分析,确定了各社区群体关注的模式以及最常被建议改进服务的方面。
研究结果表明在医疗保健获取和利用方面存在若干障碍,包括语言可及性、工作人员态度和意识、心理健康和耻辱感、支持的连续性以及诸如服务使用便利性和安全空间等实际因素。这些障碍成为共同产生响应这些群体健康和社会护理需求的服务变革的杠杆。
与来自一系列社区的人们接触对于确保IBD服务改进具有可及性并能代表个人需求和价值观至关重要。
当地社区领导者和社区团体成员积极参与了当地一家医院IBD服务改进的共同设计和开发。他们的贡献进一步为IBD中心质量改进计划的试点过程提供了信息。