理解慢性疼痛伴随残疾:通过焦点小组方法找到意义。

C. Douglas, C. Windsor, J. Wollin
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引用次数: 33

摘要

尽管有大量文献记载了以慢性非恶性疼痛为主要疾病的人的经历,但对于慢性致残的人所经历的疼痛现象却知之甚少。本焦点小组研究探讨了32名生活在社区的多发性硬化症(MS)患者的残疾相关疼痛经历。对记录的专题分析揭示了与慢性多发性硬化症相关的疼痛生活经验的4个广泛概念。第一个主题,疼痛无处不在,描述了日常生活中疼痛的压倒性和侵入性存在。参与者讲述了与残疾相关的慢性疼痛带来的身体、情感和社会后果,这给他们带来了巨大的损失和限制。第二个主题围绕着没人能理解的情感产生共鸣。参与者寻求家人、朋友和医疗保健专业人员对他们疼痛经历的理解和认可,并努力解决有关疼痛的合法性和隐蔽性的难题。第三个主题,我很好,指的是参与者对他人隐瞒痛苦的倾向。在某种程度上,由于它的争议性,参与者有时会向他人隐瞒他们的痛苦,以避免冲突,并保持他们过去生活的一些表象。最后出现的主题总是等式中的一个因素。参与者分享了多发性硬化症如何改变了他们的世界,在这个世界里,疼痛和不适已经成为日常生活的一部分,需要仔细的协商和计划来进行活动,防止病情恶化。至关重要的是,医疗保健提供者为MS患者提供机会,让他们谈论疼痛和与疼痛相关的问题,验证他们的经历,并提供能够进行自我管理的干预措施。鼓励临床医生挑战自己对残疾相关疼痛的意义和期望,以便促进治疗干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Understanding chronic pain complicating disability: finding meaning through focus group methodology.
Although extensive literature exists on the experiences of people living with chronic nonmalignant pain as a primary condition, little is known about the phenomenon of pain as it is experienced by the person with a chronic disabling condition. This focus group study explored the experience of disability-related pain among 32 people with multiple sclerosis (MS) living in the community. Thematic analysis of transcripts revealed 4 broad conceptualizations of the experience of living with chronic MS-related pain. The first theme, pain is pervasive, described the overwhelming and intrusive presence of pain in daily life. Participants related the physical, emotional, and social consequences of living with chronic, disability-related pain, which caused them great loss and restriction. The second theme resonated around feelings that nobody understands. The participants sought understanding and validation of their pain experiences by family, friends, and healthcare professionals and struggled with difficult issues concerning the legitimacy and invisibility of their pain. The third theme, I'm fine, referred to the propensity of participants to keep pain private from others. In part because of its contested nature, participants at times concealed their pain from others to avoid conflict and maintain some semblance of their former lives. The final theme that emerged was always a factor in the equation. The participants shared how MS had transformed their worlds into ones in which pain and discomfort had become a normal part of everyday life, requiring careful negotiation and planning to undertake activities and prevent exacerbation. It is vital that healthcare providers give people with MS opportunities to talk about pain and pain-related concerns, validate their experiences, and provide interventions that enable self-management. Clinicians are encouraged to challenge their own meanings and expectations about disability-related pain so that therapeutic interventions can be facilitated.
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