Pressure Ulcer Prevention at Home for People with Long-term Neurological Conditions, Carers and Personal Assistants: Synopsis - a Participatory, Qualitative study (PUP@Home1).

Delia Muir, Laura McLarty, Jessica Drinkwater, Carole Bennett, Yvonne Birks, Andrea Broadway-Parkinson, Vanessa Cooksey, Phil Gleeson, Christy Holland, Lisa Ledger, Daniella-Jade Lowe, Andrea McGoverin, Jane Nixon, Tanya Perry, Brian Rawson, Yvonne Rawson, Heidi Sandoz, Nikki Stubbs, Kay Walker, Helen Whitaker, Susanne Coleman
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引用次数: 0

Abstract

Background: Many people with long-term neurological conditions (e.g. multiple sclerosis, spina bifida) live independently and manage complex health needs, including mobility and sensory limitations which mean they have a high risk of pressure ulcer development. Despite their high risk, appropriate pressure ulcer prevention support and resources are often lacking.

Aims: To develop a Theory of Change pathway, which will underpin future development of a multicomponent intervention package supporting pressure ulcer risk identification and management, in partnership with people with long-term neurological conditions who self-manage care and live at home, their informal carers and personal assistants.

Methods: We used a partnership approach based in the participatory research paradigm, with extensive input from those whose lives are the focus of the research. The study comprised four interlinked work packages: Work package 1 - Development of two co-operative inquiry groups Work package 2 - Semistructured interviews and/or participation via a smartphone app Work package 3 - Professional and strategic stakeholder engagement Work package 4 - Systems mapping and Theory of Change pathway development Iterative, qualitative data analysis was undertaken with emerging findings from each work package informing subsequent elements of the study.

Findings: Overall, 74 participants contributed across the 4 work packages. This incorporated 31 service users, 8 carers, 9 personal assistants and 26 professional stakeholders. The findings indicate the complexities of pressure ulcer prevention for this population, who are often fulfilling multiple roles in society (i.e. in their families, communities, work) alongside onerous self-care routines. Systemic and professional barriers were found to hamper people's ability to self-care, support others and seek help. Areas of learning were highlighted around developing safe routines, third sector and peer support, learning about pressure ulcer prevention, navigating complex systems, adapting and reacting to change, perceptions of risk, risk negotiation and the role of non-clinical carers. By collaboratively reflecting on these findings with key stakeholders (service users, carers, personal assistants, professional/strategic partners), we were able to identify points in the system amenable to change. This underpinned the development of a Theory of Change for a multicomponent intervention incorporating awareness raising, routine guidance, escalation guidance and communication components (supported by preconditions, contextual requirements, long-term outcomes, impacts and explanatory rationale).

Limitations: We acknowledge that despite our best efforts (incorporating targeted National Health Service and third-sector recruitment), the ethnic diversity of our research was not as representative as we had intended. We have included work to address this lack of diversity in our next study, including dedicated community workshops to explore the cultural relevance and appropriateness of our proposed intervention.

Conclusions: The study highlights the significant impact and complexities of managing pressure ulcer prevention activities at home, for people with long-term neurological conditions, carers and personal assistants. By understanding these complexities from different perspectives, we were able to develop a systems map and Theory of Change pathway informing future intervention development and evaluation.

Future work: Funding has been awarded for Pressure Ulcer Prevention at Home 2 (PUP@home2): Self-management intervention development and user testing for people with long-term neurological conditions (NIHR163165) to support pressure ulcer prevention and self-care, based on our learning from this study.

Funding: This synopsis presents independent research funded by the National Institute for Health and Care Research (NIHR) Health and Social Care Delivery Research programme as award number NIHR134029.

长期神经系统疾病患者、护理人员和个人助理在家预防压疮:摘要-一项参与性质的研究(PUP@Home1)。
背景:许多患有长期神经系统疾病(如多发性硬化症、脊柱裂)的人独立生活,并处理复杂的健康需求,包括活动能力和感觉限制,这意味着他们有很高的压疮发展风险。尽管他们的高风险,适当的压疮预防支持和资源往往缺乏。目的:与长期神经系统疾病患者、他们的非正式护理者和个人助理合作,开发一种“变化理论”途径,支持压疮风险识别和管理的多成分干预方案的未来发展。方法:我们采用了基于参与式研究范式的伙伴关系方法,并从那些生活是研究重点的人那里得到了广泛的投入。该研究包括四个相互关联的工作包:工作包1 -开发两个合作调查小组工作包2 -半结构化访谈和/或通过智能手机应用程序参与工作包3 -专业和战略利益相关者参与工作包4 -系统映射和变革理论路径开发工作包4 -对每个工作包的新发现进行了迭代定性数据分析,为研究的后续要素提供信息。调查结果:总体而言,74名参与者在4个工作包中做出了贡献。其中包括31名服务使用者、8名护理人员、9名私人助理和26名专业利益相关者。研究结果表明,对于这一人群来说,预防压疮的复杂性,他们往往在繁重的自我保健程序之外,还在社会(即家庭、社区、工作)中扮演多重角色。系统和专业障碍阻碍了人们自我照顾、支持他人和寻求帮助的能力。重点学习的领域包括制定安全常规、第三部门和同伴支持、学习预防压疮、驾驭复杂系统、适应和应对变化、风险感知、风险谈判和非临床护理人员的角色。通过与主要利益相关者(服务使用者、护理人员、个人助理、专业/战略合作伙伴)共同反思这些发现,我们能够确定系统中可修改的点。这为多成分干预的变革理论的发展提供了基础,包括提高意识、常规指导、升级指导和沟通成分(由先决条件、背景要求、长期结果、影响和解释理由支持)。局限性:我们承认,尽管我们尽了最大努力(纳入有针对性的国民健康服务和第三部门招聘),但我们研究的种族多样性并不像我们预期的那样具有代表性。我们在下一项研究中纳入了解决这一缺乏多样性的工作,包括专门的社区研讨会,以探讨我们提出的干预措施的文化相关性和适当性。结论:该研究强调了在家中管理压疮预防活动的重大影响和复杂性,对于长期患有神经系统疾病的人,护理人员和个人助理。通过从不同的角度理解这些复杂性,我们能够开发一个系统地图和变化理论路径,为未来的干预开发和评估提供信息。未来的工作:根据我们从本研究中获得的经验,资助了家庭压疮预防2 (PUP@home2):长期神经系统疾病患者的自我管理干预开发和用户测试(NIHR163165),以支持压疮预防和自我保健。资助:本摘要介绍了由国家卫生和保健研究所(NIHR)卫生和社会保健提供研究计划资助的独立研究,奖励号为NIHR134029。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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