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多发性硬化症患者对决策辅助工具关键要素的看法:一项定性研究。

Views of Multiple Sclerosis Patients About Key Elements for a Decision Aid: A Qualitative Study.

出版信息

J Neurosci Nurs. 2023 Oct 1;55(5):164-170. doi: 10.1097/JNN.0000000000000721. Epub 2023 Aug 8.

Abstract

BACKGROUND

Patients with multiple sclerosis (MS) may experience decisional conflict during treatment choice. Shared decision making (SDM), whereby patients and health professionals, primarily nurses, collaborate in making decisions, reduces this decisional conflict. It requires understanding large amounts of information and may be complex, especially when decisions affect patients' autonomy and quality and prolongation of life. Patient decision aids are tools in facilitating SDM. This study aimed to identify the key elements from the perspective of patients with relapsing-remitting MS to create a patient decision aid in the Spanish sociocultural context. METHODS: This is a qualitative study using focus groups led by a clinical nurse specialist. Semistructured interviews included healthcare needs and demands, the SDM process, and general characteristics of a peer support program. After the transcription of interview recordings, data were analyzed by thematic analysis and a constructivist naturalistic approach. RESULTS: Patients with MS (27) from Spain participated in 4 focus groups of 90 to 120 minutes each. Three overarching themes were identified: information access to sufficient high-quality data; knowledge of available treatment options, including efficacy, adverse effects, frequency, administration route, and the impact on daily life; decision-making role, engaged versus nonengaged patients. The former require support in facilitating their active involvement in decisions, whereas the latter prefer more passive health models. CONCLUSION: The needs identified by patients with relapsing-remitting MS regarding treatment choice in the Spanish setting align with those reported by other studies. The identified themes provide valuable information to design and develop a virtual patient decision aid jointly by clinical MS nurses and patients according to the International Patient Decision Aid Standards Collaboration criteria. This aid will help improve understanding between nurses and patients during SDM and facilitate the process.

摘要

背景

多发性硬化症 (MS) 患者在治疗选择时可能会经历决策冲突。共同决策 (SDM) 是指患者和卫生专业人员(主要是护士)合作做出决策,从而减少这种决策冲突。它需要理解大量信息,并且可能很复杂,尤其是当决策影响患者的自主权以及生活质量和寿命延长时。患者决策辅助工具是促进 SDM 的工具。本研究旨在从复发缓解型 MS 患者的角度确定关键要素,以在西班牙社会文化背景下创建患者决策辅助工具。

方法

这是一项定性研究,使用由临床护士专家领导的焦点小组。半结构化访谈包括医疗保健需求和要求、SDM 过程以及同伴支持计划的一般特征。在转录访谈记录后,通过主题分析和建构主义自然主义方法进行数据分析。

结果

来自西班牙的 27 名 MS 患者参加了 4 次每组 90 至 120 分钟的焦点小组。确定了三个总体主题:获取足够高质量数据的信息渠道;了解可用的治疗选择,包括疗效、不良反应、频率、给药途径以及对日常生活的影响;决策角色,积极参与决策的患者与不积极参与决策的患者。前者需要支持以促进他们积极参与决策,而后者更喜欢更被动的健康模式。

结论

复发缓解型 MS 患者在西班牙环境下对治疗选择的需求与其他研究报告的需求一致。确定的主题为根据国际患者决策辅助工具标准协作标准,由临床 MS 护士和患者共同设计和开发虚拟患者决策辅助工具提供了有价值的信息。该辅助工具将有助于改善 SDM 期间护士和患者之间的理解,并促进这一过程。

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