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Music and Psychology & Social Connections Program: Protocol for a Novel Intervention for Dyads Affected by Younger-Onset Dementia.音乐与心理及社会联系项目:针对受早发性痴呆影响的二元组的新型干预方案。
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本文引用的文献

1
Family Carers of People with Young-Onset Dementia: Their Experiences with the Supporter Service.早发性痴呆症患者的家庭照顾者:他们在支持者服务方面的经历。
Geriatrics (Basel). 2016 Nov 5;1(4):28. doi: 10.3390/geriatrics1040028.
2
Experiences and needs of spouses of persons with young-onset frontotemporal lobe dementia during the progression of the disease.早发性额颞叶痴呆患者配偶在疾病进展过程中的经历与需求。
Scand J Caring Sci. 2017 Dec;31(4):779-788. doi: 10.1111/scs.12397. Epub 2017 Mar 9.
3
A patient's experience in dementia care: Using the "lived experience" to improve care.一位患者在痴呆症护理中的经历:利用“亲身经历”改善护理。
Can Fam Physician. 2017 Jan;63(1):22-26.
4
Measuring younger onset dementia: What the qualitative literature reveals about the 'lived experience' for patients and caregivers.测量早发性痴呆:定性文献揭示的患者及照料者“生活体验”
Dementia (London). 2019 Feb;18(2):579-598. doi: 10.1177/1471301216684401. Epub 2017 Jan 23.
5
Rate of early onset Alzheimer's disease: a systematic review and meta-analysis.早发性阿尔茨海默病的发病率:系统评价和荟萃分析。
Ann Transl Med. 2015 Mar;3(3):38. doi: 10.3978/j.issn.2305-5839.2015.01.19.
6
Tracing the successful incorporation of assistive technology into everyday life for younger people with dementia and family carers.追踪辅助技术在有痴呆症的年轻人和家庭照顾者的日常生活中的成功融入情况。
Dementia (London). 2016 Jul;15(4):646-62. doi: 10.1177/1471301214532263. Epub 2014 Apr 29.
7
Gradually losing one's foothold--a fragmented existence when living alone with dementia.逐渐失去立足之地——与痴呆症独居时支离破碎的生活。
Dementia (London). 2015 Mar;14(2):145-63. doi: 10.1177/1471301213494510. Epub 2013 Jul 11.
8
Experiences of persons with early-onset dementia in everyday life: a qualitative study.早发性痴呆患者日常生活体验的定性研究。
Dementia (London). 2013 Jul;12(4):410-24. doi: 10.1177/1471301211430647. Epub 2011 Dec 16.
9
Quality of life in dementia: a study on proxy bias.痴呆患者的生活质量:代理偏见研究。
BMC Med Res Methodol. 2013 Sep 6;13:110. doi: 10.1186/1471-2288-13-110.
10
The global prevalence of dementia: a systematic review and metaanalysis.全球痴呆症患病率:系统评价和荟萃分析。
Alzheimers Dement. 2013 Jan;9(1):63-75.e2. doi: 10.1016/j.jalz.2012.11.007.

“生存还是毁灭”:独居早发性痴呆患者的病情恶化经历

"To be, or not to be": experiencing deterioration among people with young-onset dementia living alone.

作者信息

Johannessen Aud, Engedal Knut, Haugen Per Kristian, Dourado Marcia Cristina Nascimento, Thorsen Kirsten

机构信息

a Norwegian National Advisory Unit on Ageing and Health , Vestfold Hospital Trust , Tønsberg , Norway.

b University of South-Eastern , Vestfold , Norway.

出版信息

Int J Qual Stud Health Well-being. 2018 Dec;13(1):1490620. doi: 10.1080/17482631.2018.1490620.

DOI:10.1080/17482631.2018.1490620
PMID:29975182
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6041786/
Abstract

Having dementia before the age of 65 (YOD) represents a radical break from an age-normative and expected life course. The disease afflicts the person's identity, threatens the self-image and self-confidence, and erodes the person's plans. The aim of the study was toexamine how people living alone with YOD perceive the course of dementia, their needs, and coping strategies, with a focus on narrating everyday life experiences. A longitudinal study using a qualitative approach was used. Five interviews, each with 10 informants, took place every 6 months from 2014 to 2017. The main theme is the person's experiences of changes of identity over time. The most significant aspects of their experiences of the dementia affecting them and their reactions are these: the initial signs, coping efforts, concealing the diagnosis, social retraction, existential anxiety, revival of the self, worse and worse, and health personnel as background. The study concluded thatpeople with dementia are able to describe their experiences and needs for a long time during the progression of dementia. Their voices should be listened to for planning of services. Personalized care should be used to support them in order to preserve their identity in a normalized everyday life as far as possible.

摘要

65岁前患痴呆症(早发性痴呆)代表着与正常年龄和预期人生轨迹的彻底决裂。这种疾病会影响人的身份认同,威胁自我形象和自信心,并破坏个人计划。本研究的目的是调查独居的早发性痴呆患者如何看待痴呆症的病程、他们的需求以及应对策略,重点是叙述日常生活经历。采用了定性方法的纵向研究。从2014年到2017年,每6个月进行一次访谈,每次有10名受访者,共进行了五次访谈。主要主题是随着时间推移个人身份认同的变化经历。他们在痴呆症影响下的经历及其反应的最重要方面包括:初始症状、应对努力、隐瞒诊断、社交退缩、生存焦虑、自我复苏、每况愈下以及以医护人员为背景。研究得出结论,痴呆症患者在痴呆症进展过程中能够长时间描述自己的经历和需求。在规划服务时应倾听他们的声音。应采用个性化护理来支持他们,以便在正常化的日常生活中尽可能保持他们的身份认同。