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多发性硬化症症状体验中的“不可见性”概念:系统元综合分析。

The notion of "invisibility" in people's experiences of the symptoms of multiple sclerosis: a systematic meta-synthesis.

机构信息

Division of Psychiatry and Applied Psychology, School of Medicine, University of Nottingham, Nottingham, UK.

Institute of Mental Health, Nottinghamshire Healthcare Trust, University of Nottingham, Nottingham, UK.

出版信息

Disabil Rehabil. 2021 Nov;43(23):3276-3290. doi: 10.1080/09638288.2020.1741698. Epub 2020 Mar 24.

Abstract

PURPOSE

Invisible symptoms have a negative impact on people living with Multiple Sclerosis (MS), related to the very notion that they are "unseen." It is important to understand the notion of "invisibility" in MS, as invisible symptoms are particularly distressing, and there is a paucity of research focussing on their invisible nature and its specific impact. We aimed to systematically identify, appraise and synthesise qualitative research regarding the notion of "invisibility" in relation to people's lived experience of symptoms of MS.

METHODS AND MATERIALS

Articles meeting inclusion criteria were critically appraised and synthesised using a meta-ethnographic approach.

RESULTS

17 articles were identified from six electronic databases. Three third-order themes were presented as a . "Invisibility" was conceptualised by people with MS as a discrepancy between the internal experience of symptoms and what is observed externally. "Invisibility" of MS symptoms was found to have numerous impacts, including not feeling understood or validated by others, issues around the perceived legitimacy of the illness, and living with needs which are hidden. We found that "invisibility" by its nature offers people a choice of strategies they use to navigate it. This choice introduces a dilemma: disclose the diagnosis to be "seen," or remain "invisible."

CONCLUSIONS

This review revealed the manner in which people with MS are affected by the invisibility of their symptoms and the various adaptations used to navigate these lived experiences. We highlight the need to improve clinician and public understanding, and to better respond to these experiences. Future research focusing on the exploration of people's experiences of "invisibility" in MS, including the ways in which "invisibility" is managed on a day-to-day basis could raise clinical and public awareness of the impact of "invisibility" and how to provide support for this, thus easing the dilemmas faced by those with MS.IMPLICATIONS FOR REHABILITATIONPeople with Multiple Sclerosis (MS) experience symptoms that are not overtly visible to others, impacting their emotional and social wellbeing negatively.It is important for healthcare professionals to validate MS patients' experiences around "invisibility" and provide appropriate support.Healthcare professionals should address with MS patients any issues around disclosure of their diagnosis to those around them and support them to navigate these decisions.Raising awareness about the impact of "invisibility" for people with MS may help to lessen patient burden and promote understanding amongst healthcare professionals and the general public.

摘要

目的

隐形症状对多发性硬化症(MS)患者有负面影响,这与它们“看不见”的概念有关。理解 MS 中的“隐形”概念很重要,因为隐形症状特别令人痛苦,而且几乎没有研究关注它们的隐形性质及其特定影响。我们旨在系统地确定、评估和综合与人们对 MS 症状的生活体验相关的“隐形”概念的定性研究。

方法和材料

符合纳入标准的文章经过批判性评估,并使用元伦理方法进行综合。

结果

从六个电子数据库中确定了 17 篇文章。呈现了三个第三级主题。人们将“隐形”概念化为内部症状体验与外部观察到的症状之间的差异。研究发现,MS 症状的“隐形”会产生许多影响,包括不被他人理解或认可、对疾病合法性的看法、以及隐藏的需求问题。我们发现,“隐形”本质上为人们提供了一种策略选择,以应对它。这种选择带来了一个两难境地:向他人透露诊断以获得“关注”,或保持“隐形”。

结论

本综述揭示了 MS 患者受到症状隐形性影响的方式,以及他们用于应对这些生活体验的各种适应策略。我们强调需要提高临床医生和公众的理解,并更好地应对这些体验。未来的研究专注于探索 MS 患者“隐形”体验,包括日常管理“隐形”的方式,可以提高临床和公众对“隐形”影响的认识,以及如何为此提供支持,从而缓解 MS 患者面临的困境。

对康复的意义

多发性硬化症(MS)患者会经历一些他人无法明显观察到的症状,这会对他们的情感和社会健康产生负面影响。

对医疗保健专业人员的意义

重要的是,医疗保健专业人员要验证 MS 患者在“隐形”方面的体验,并提供适当的支持。

对医疗保健专业人员的意义

医疗保健专业人员应与 MS 患者讨论他们向周围人透露诊断的问题,并支持他们做出这些决定。

对公众的意义

提高公众对 MS 患者隐形问题的认识,可能有助于减轻患者负担,并促进医疗保健专业人员和公众的理解。

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