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确诊系统性红斑狼疮患者的不确定性与机遇:一项定性研究

Uncertainty and opportunities in patients with established systemic lupus erythematosus: a qualitative study.

作者信息

Mattsson M, Möller B, Stamm T, Gard G, Boström C

机构信息

Department of Health Sciences, Luleå University of Technology, Luleå, Sweden.

出版信息

Musculoskeletal Care. 2012 Mar;10(1):1-12. doi: 10.1002/msc.220. Epub 2011 Oct 18.

Abstract

UNLABELLED

Systemic lupus erythematosus (SLE) is a chronic disease which can affect any organ, and the impact of the condition will affect each person differently. There are few qualitative studies including the experiences of both women and men with a diagnosis of SLE corresponding to the American College of Rheumatology (ACR) criteria where both negative and positive impacts of the disease have been presented.

PURPOSE

The aim was to describe how patients with established SLE experience their illness in everyday life, including both negative and positive aspects.

METHOD

Four focus group interviews were conducted with 16 women and three men with SLE according to ACR criteria, with varied disease activity and no or little organ damage. The interviews were tape recorded, transcribed verbatim and analysed using qualitative content analysis.

RESULTS

Two themes emerged: multifaceted uncertainty contained the categories 'an unreliable body', 'obtrusive pain and incomprehensible fatigue', 'mood changes and worries', 'reliance on medication and health care'; Focus on health and opportunities included 'learning process implying personal strength', 'limitations and possibilities in activities and work', 'a challenge to explain and receive support' and 'living an ordinary life incorporating meaningful occupations'.

CONCLUSIONS

While we expected to find a mainly negative impact, positive aspects were also described. Our findings were complex and showed that patients with established SLE can experience both uncertainty and opportunities. This highlights the importance for healthcare professionals of gaining a better understanding of patients' uncertainty, to enable them to support patients, allowing them to focus on health and opportunities. Measurement instruments that capture different aspects of uncertainty and opportunities needs to be developed.

摘要

未标注

系统性红斑狼疮(SLE)是一种可累及任何器官的慢性疾病,其对每个人的影响各不相同。很少有定性研究纳入了符合美国风湿病学会(ACR)标准的男女狼疮患者的经历,这些研究既呈现了该疾病的负面影响,也呈现了其正面影响。

目的

旨在描述确诊为SLE的患者在日常生活中如何体验自身疾病,包括负面和正面两个方面。

方法

根据ACR标准,对16名女性和3名男性SLE患者进行了4次焦点小组访谈,这些患者疾病活动程度各异,且无器官损害或仅有轻微器官损害。访谈进行了录音,逐字转录,并采用定性内容分析法进行分析。

结果

出现了两个主题:多方面的不确定性包含“不可靠的身体”“难以忍受的疼痛和难以理解的疲劳”“情绪变化和担忧”“对药物和医疗保健的依赖”等类别;关注健康与机会包括“意味着个人力量的学习过程”“活动和工作中的限制与可能性”“解释病情并获得支持的挑战”以及“融入有意义活动的平凡生活”。

结论

虽然我们预期主要发现负面影响,但也描述了正面影响。我们的研究结果很复杂,表明确诊为SLE的患者既会经历不确定性,也会遇到机会。这凸显了医疗保健专业人员更好地理解患者不确定性的重要性,以便他们能够支持患者,使患者能够关注健康和机会。需要开发能够捕捉不确定性和机会不同方面的测量工具。

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