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帕金森病患者生活体验的定性研究的元分析。

The Subjective Experience of Living with Parkinson's Disease: A Meta-Ethnography of Qualitative Literature.

机构信息

Amsterdam UMC, Vrije Universiteit Amsterdam, Psychiatry, Amsterdam Public Health, Amsterdam, Netherlands.

Amsterdam UMC, Vrije Universiteit Amsterdam, Anatomy & Neuroscience, Amsterdam Public Health, Amsterdam, Netherlands.

出版信息

J Parkinsons Dis. 2021;11(1):139-151. doi: 10.3233/JPD-202299.

Abstract

BACKGROUND

A better understanding of the subjective experience of living with Parkinson's disease (PD) and the factors that influence this experience can be used to improve wellbeing of people with PD (PwP).

OBJECTIVE

To gain more insight in the subjective experience of PD from the PwP's perspective, and the factors that contribute to this experience.

METHODS

In this qualitative review, we performed a systematic search of qualitative studies discussing the subjective experience of PD and extracted reported themes (first order themes). Using a meta-ethnographic approach, we categorized the first order themes into second order themes, and created a third order construct: a holistic model of the subjective experience of living with PD.

RESULTS

We included 20 studies with a total sample of 279 PwP. Data-extraction yielded 227 first order themes, which were categorized into the second order themes: 1) Awareness, 2) Disruption, 3) Adjustment, 4) The external environment, and 5) The changing self. With these themes, we developed the "model of dialectic change" which conceptualizes life with PD as a transformative journey, wherein PwP employ strategies to stabilize their changeable relationship with their external environment, while simultaneously redefining their self-concept.

CONCLUSION

Our findings indicate that not only the symptoms of PD, but also the manner in which these cause disruptions in the PwP's interaction with their personal environment and self-concept, determine the subjective experience of PD andquality of life. Some PwP experience problems with adjusting, resulting in psychological distress. This calls for a holistic, multidisciplinary and participatory approach of PD.

摘要

背景

深入了解帕金森病(PD)患者的主观体验,以及影响这种体验的因素,可以提高 PD 患者(PwP)的幸福感。

目的

从 PwP 的角度深入了解 PD 的主观体验,以及影响这种体验的因素。

方法

在这项定性综述中,我们对讨论 PD 主观体验的定性研究进行了系统检索,并提取了报告的主题(一级主题)。我们使用元民族学方法将一级主题分类为二级主题,并创建了一个三级结构:一个整体的 PD 主观体验模型。

结果

我们纳入了 20 项研究,共纳入 279 名 PwP。数据提取得到 227 个一级主题,这些主题被分为二级主题:1)意识,2)干扰,3)调整,4)外部环境,5)自我变化。通过这些主题,我们提出了“辩证变化模型”,将 PD 生活概念化为一个变革之旅,其中 PwP 采用策略来稳定他们与外部环境之间变化的关系,同时重新定义他们的自我概念。

结论

我们的研究结果表明,不仅 PD 的症状,而且这些症状导致 PwP 与个人环境和自我概念的互动受到干扰的方式,决定了 PD 的主观体验和生活质量。一些 PwP 在调整方面存在问题,导致心理困扰。这需要采取整体、多学科和参与性的 PD 方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4612/7990446/3a5bac66e684/jpd-11-jpd202299-g001.jpg

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