Johannessen Aud, Engedal Knut, Haugen Per Kristian, Dourado Marcia Cristina Nascimento, Thorsen Kirsten
a Norwegian National Advisory Unit on Ageing and Health , Vestfold Hospital Trust , Tønsberg , Norway.
b University of South-Eastern , Vestfold , Norway.
Int J Qual Stud Health Well-being. 2018 Dec;13(1):1490620. doi: 10.1080/17482631.2018.1490620.
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.
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。