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“我将为人们争取避免我所经历的体验而奋斗”:对慢性疼痛患者生活体验倡导者的经历和观点的主题分析。

'I Will Fight for People to Not Have the Experience I've Had': A Thematic Analysis of the Experiences and Perspectives of Chronic Pain Lived Experience Advocates.

机构信息

Faculty of Medical Sciences, Newcastle University, Newcastle, UK.

出版信息

Qual Health Res. 2023 Sep;33(11):995-1004. doi: 10.1177/10497323231188639. Epub 2023 Aug 23.

DOI:10.1177/10497323231188639
PMID:37610073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10494474/
Abstract

Navigating the healthcare system with chronic pain, alongside navigating the experience of the chronic pain itself, is recognised to be highly challenging. Frequently available interventions do not fully meet the needs of people with chronic pain. This study aimed to explore the perspectives of people who have been through these experiences and now support and campaign for improved approaches to chronic pain management. Semi-structured interviews of 10 participants who independently support others through some form of chronic pain advocacy or support were conducted online. Data were digitally recorded, transcribed, and analysed using reflexive thematic analysis, through a critical realist and constructivist lens. Data were interpreted to represent a journey into chronic pain advocacy, represented by three overarching themes. Advocacy as healing incorporates sub-themes of pain trauma, gaining knowledge, and using my experience for good. Unequal partnership includes respect and unmet needs from institutions. The final theme, evolution, relates to two sub-themes of pushing boundaries and personal growth. Participants talked about the dual benefit of their contribution to pain advocacy, both in terms of helping others and also their own personal benefit. Overall findings indicated that pain advocacy can take multiple and various forms. Commonly, our participants who took on the role of pain advocacy were motivated by their own early difficult experiences, both navigating their pain and healthcare systems, and by a wish for others to not have similar difficult experiences. Having taken on the role, despite its challenges, rewards can include recognition and personal growth.

摘要

患有慢性疼痛的患者在就医时,需要同时应对慢性疼痛本身带来的体验,这被认为是极具挑战性的。目前常用的干预措施并不能完全满足慢性疼痛患者的需求。本研究旨在探讨有过这些经历并支持和倡导改善慢性疼痛管理方法的人的观点。通过批判性现实主义和建构主义视角,对 10 名独立通过某种形式的慢性疼痛倡导或支持来帮助他人的参与者进行了在线半结构化访谈。通过反思性主题分析,对数字记录、转录和分析的数据进行了解释,以代表对慢性疼痛倡导的探索,由三个总体主题表示。倡导即治愈包含疼痛创伤、获得知识和善用我的经验等子主题。不平等的伙伴关系包括机构的尊重和未满足的需求。最后一个主题是进化,涉及两个子主题:突破界限和个人成长。参与者谈到了他们对疼痛倡导做出贡献的双重好处,既帮助了他人,也对自己有好处。总体研究结果表明,疼痛倡导可以采取多种形式。通常,我们的疼痛倡导参与者是出于自己早期的困难经历而选择这个角色的,包括应对自己的疼痛和医疗保健系统,以及希望他人不要有类似的困难经历。尽管面临挑战,但承担这个角色的回报可以包括认可和个人成长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/281b/10494474/02c2bc5a4075/10.1177_10497323231188639-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/281b/10494474/02c2bc5a4075/10.1177_10497323231188639-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/281b/10494474/02c2bc5a4075/10.1177_10497323231188639-fig1.jpg

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A Healing Journey with Chronic Pain: A Meta-Ethnography Synthesizing 195 Qualitative Studies.
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