“你必须相信病人”:纤维肌痛患者在就医时发现什么是有帮助的(和阻碍的)?

IF 2 Q3 CLINICAL NEUROLOGY
Ria K Nishikawara, Izabela Z Schultz, Lee D Butterfield, John W Murray
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引用次数: 2

摘要

背景:纤维肌痛(FM)是一种复杂的,仍然知之甚少,难以治疗的慢性疼痛状况,许多人努力寻找适当的护理。目的:本研究调查了一个研究问题,“纤维肌痛患者在接受医疗保健服务时认为哪些是有帮助的,哪些是有阻碍的,哪些是缺失的,但又希望得到的?”目的是为临床实践确定明确的、可实施的改变。材料与方法:本研究采用强化关键事件技术(enhanced critical event technique, ECIT),一种着重于帮助、阻碍和期望因素的定性研究方法,探讨14例确诊为FM的个体(12女2男)的医疗保健经历。结果:采用定性数据分析,将医疗保健体验分为三类:(1)系统导航,包括金融和经济安全;护理的可及性、灵活性和连续性;治疗方案的多样性;(2)医患联盟,包括无效和偏见;治疗债券;治疗方案的医患一致性;(3)患者自我管理策略,包括信息寻求教育、自我倡导、社会支持、症状管理策略和其他应对策略。参与者倾向于将他们的医疗保健问题概念化为一个多层次的系统问题。结论:参与者描述了他们认为的医疗系统设备不足,无法满足他们的需求,并倾向于使他们的健康担忧无效。帮助经验往往是个别临床医生独特努力的结果。研究结果强调了认识疼痛的复杂性和心理影响、信任医患关系、在生物心理社会框架内的多学科/跨学科护理、改善FM心理社会方面的教育和认识以及有效管理慢性疼痛的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

"You have to believe the patient": What do people with fibromyalgia find helpful (and hindering) when accessing health care?

"You have to believe the patient": What do people with fibromyalgia find helpful (and hindering) when accessing health care?

Background: Fibromyalgia (FM) is a complex, still poorly understood, and difficult-to-treat chronic pain condition for which many people struggle to find adequate care.

Aims: This study investigated the research question, "What do people accessing health care services for fibromyalgia perceive as helpful, hindering, and absent but desired?" with the aim of identifying clear, implementable changes for clinical practice.

Materials and methods: This study used the enhanced critical incident technique (ECIT), a qualitative research method that focuses on helping, hindering, and desired factors, to explore the health care experiences of 14 individuals (12 women and 2 men) diagnosed with FM.

Results: Using qualitative data analysis, results identified three categories of health care experiences: (1) systemic navigation, including financial and economic security; accessibility, flexibility, and continuity of care; and diversity of treatment options; (2) clinician-patient alliance, including invalidation and prejudice; therapeutic bond; and clinician-patient alignment on treatment plan; and (3) patient self-management strategies, including information-seeking and education, self-advocacy, social supports, symptom management strategies, and other coping strategies. Participants tended to conceptualize their health care concerns as a multilayered systemic problem.

Conclusions: Participants described a medical system they perceived as poorly equipped to support their needs and tended to invalidate their health concerns. Helping experiences tended to be the result of unique efforts on the part of individual clinicians. Findings emphasize the importance of recognizing the complexities and psychological impact of pain, trusting clinician-patient relationships, multidisciplinary/interdisciplinary care within a biopsychosocial framework, and improved education and awareness around psychosocial aspects of FM and effective management of chronic pain.

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来源期刊
CiteScore
3.70
自引率
12.50%
发文量
36
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