The Lived Experience of Pain Services: A Comparison of Service Users' and Service Providers' Experience of Irish Health Services.

IF 3 3区 医学 Q2 CLINICAL NEUROLOGY
Pain Research & Management Pub Date : 2025-08-03 eCollection Date: 2025-01-01 DOI:10.1155/prm/4608906
Kate Sheridan, Aine MacNamara, Enda Whyte, Siobhan O'Connor
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引用次数: 0

Abstract

Background: A supportive healthcare experience that implements a biopsychosocial model of care can empower a person with chronic pain to make informed decisions and engage in self-management behaviours. Despite the positive influence of supportive healthcare, little is known about the presence of healthcare support in under-resourced chronic pain services. This idiographic study explores the lived experience of service users and providers participating in chronic pain services with a specific focus on autonomy support and self-management skills. Methods: Semistructured interviews were conducted on service users (n = 7) self-reporting a diagnosis of chronic pain (pain > 3 months) and service providers (n = 5), defined as healthcare professionals with > 3 years of experience in clinical healthcare settings managing pain conditions. All interviews took place online (mean 47 ± 11 min). Interview transcripts were analysed using interpretative phenomenological analysis. Results: Analyses generated four themes: 'biomedical model leads care'; 'lost in a system'; 'I need support' and 'the essentials of self-management'. Both service users and providers described regular experiences of invalidation and biomedical approaches to pain management. Long waitlists, a lack of multidisciplinary services, short appointment times and a lack of educational resources all impacted the development of self-management skills in service users. Conclusion: Despite clinical guidelines recommending a biopsychosocial model of care, the biomedical model remains the dominant approach in chronic pain management, reflecting a persistent gap between evidence and practice. Service users and providers desire access to multidisciplinary services that support a biopsychosocial model of care. Healthcare professionals cannot deliver what service users expect due to macro-, meso- and microlevel factors. Future research is needed to explore practical solutions to deliver pain services that optimise the development of self-management skills where existing infrastructure and resources negatively impact service delivery. Suggested approaches include enhancing autonomy-supportive communication by healthcare providers and ensuring early access to high-quality educational materials.

疼痛服务的生活经验:爱尔兰卫生服务的服务用户和服务提供者的经验比较。
背景:一个支持性的医疗保健经验,实现一个生物心理社会模式的护理可以授权一个人与慢性疼痛做出明智的决定,并从事自我管理行为。尽管支持性医疗保健有积极的影响,但在资源不足的慢性疼痛服务中,人们对医疗保健支持的存在知之甚少。这项具体研究探讨了服务用户和提供者参与慢性疼痛服务的生活经验,特别关注自主支持和自我管理技能。方法:对自我报告慢性疼痛诊断的服务使用者(n = 7)和服务提供者(n = 5)进行半结构化访谈,服务提供者定义为在临床医疗保健机构管理疼痛条件方面具有> 3年经验的医疗保健专业人员。所有访谈均在线进行(平均47±11分钟)。访谈记录采用解释性现象学分析进行分析。结果:分析产生了四个主题:“生物医学模式引领护理”;“迷失在一个系统中”;“我需要支持”和“自我管理的基本要素”。服务使用者和提供者都描述了失效和生物医学方法治疗疼痛的常规经验。等候名单长、缺乏多学科服务、预约时间短以及缺乏教育资源都影响了服务使用者自我管理技能的发展。结论:尽管临床指南推荐生物心理社会治疗模式,但生物医学模式仍然是慢性疼痛治疗的主要方法,这反映了证据与实践之间的持续差距。服务使用者和提供者希望获得支持生物心理社会护理模式的多学科服务。由于宏观、中观和微观层面的因素,医疗保健专业人员无法提供用户所期望的服务。未来的研究需要探索实际的解决方案,以提供疼痛服务,优化自我管理技能的发展,现有的基础设施和资源对服务的提供产生负面影响。建议的方法包括加强卫生保健提供者支持自主的沟通,并确保尽早获得高质量的教育材料。
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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来源期刊
Pain Research & Management
Pain Research & Management CLINICAL NEUROLOGY-
CiteScore
5.30
自引率
0.00%
发文量
109
审稿时长
>12 weeks
期刊介绍: Pain Research and Management is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of pain management. The most recent Impact Factor for Pain Research and Management is 1.685 according to the 2015 Journal Citation Reports released by Thomson Reuters in 2016.
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