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认知能力下降的主观体验和痴呆诊断:对英国记忆诊所最近被诊断出患有痴呆症的人的定性访谈。

Subjective experiences of cognitive decline and receiving a diagnosis of dementia: qualitative interviews with people recently diagnosed in memory clinics in the UK.

机构信息

Medical School, University of Exeter, Exeter, UK.

School of Health Sciences, City, University of London, London, UK.

出版信息

BMJ Open. 2019 Aug 1;9(8):e026071. doi: 10.1136/bmjopen-2018-026071.

Abstract

OBJECTIVES

To explore people's experiences of cognitive decline and receiving a diagnosis of dementia.

DESIGN

61 semistructured interviews within 2 weeks of diagnosis. Audio recordings were transcribed, line-by-line coded using NVIVO V.11 and analysed using thematic analysis.

SETTING

9 memory clinics (UK).

PARTICIPANTS

People with mild/moderate dementia.

RESULTS

Most participants were diagnosed with Alzheimer's disease (56% female, mean age 81 years). 104 codes were grouped into 22 categories, feeding into 9 subthemes and 4 overarching themes: (1) dissonance, threat to identity and visibility of dementia: dementia was associated with a progressive loss of competence, culminating in being an idiot, crazy and losing the plot. The stigma of dementia led people to hide their diagnosis from others, even close family members. However, decreasing competence in everyday tasks was becoming increasingly visible in family and wider social networks. (2) Vulnerability and being in limbo: people were frustrated by the impact of dementia on their lives and felt vulnerable. Moreover, people were disturbed by not knowing how much and when they would deteriorate further. (3) Loss of control and agency: loneliness, increasing dependence and becoming a burden foreshadowed increasing diminished personal agency. (4) Maintaining agency and self-worth: some people focused on what they could do and the benefits of diagnosis. This involved accepting the diagnosis, adapting to changes by using coping strategies and accepting support from others. This helped people to maintain personal agency and self-worth.

CONCLUSION

While personal acceptance of dementia is challenging, people are additionally troubled about disclosing their diagnosis to others. Limited time in diagnostic appointments and limited postdiagnostic support leave few opportunities to address the emotional impact of a dementia diagnosis. There may be opportunities for healthcare professionals to discuss with patients the benefits of staying positive, implementing coping strategies and accepting support to live well with dementia.

摘要

目的

探索人们认知能力下降和被诊断为痴呆症的经历。

设计

诊断后 2 周内进行了 61 次半结构化访谈。使用 NVIVO V.11 对音频记录进行逐行编码,并使用主题分析进行分析。

地点

9 个记忆诊所(英国)。

参与者

轻度/中度痴呆患者。

结果

大多数参与者被诊断为阿尔茨海默病(56%为女性,平均年龄 81 岁)。104 个代码被分为 22 个类别,分为 9 个子主题和 4 个主题:(1)失调、身份威胁和痴呆症的可见性:痴呆症与逐渐丧失能力有关,最终表现为白痴、疯狂和失去理智。痴呆症的污名将人们与他人,甚至与亲密的家庭成员隐瞒自己的诊断。然而,在家庭和更广泛的社交网络中,日常生活任务中能力下降的情况越来越明显。(2)脆弱性和处于中间状态:人们对痴呆症对生活的影响感到沮丧,感到脆弱。此外,人们对不知道自己会进一步恶化多少和何时感到不安。(3)失去控制和代理权:孤独、依赖性增加和成为负担预示着个人代理权的逐渐减弱。(4)保持代理权和自我价值感:一些人专注于自己能做什么,以及诊断的好处。这包括接受诊断,通过使用应对策略和接受他人的支持来适应变化。这有助于人们保持个人代理权和自我价值感。

结论

虽然个人接受痴呆症具有挑战性,但人们还对向他人透露诊断结果感到困扰。诊断预约时间有限,诊断后支持有限,几乎没有机会解决痴呆症诊断的情绪影响。医护人员可能有机会与患者讨论保持积极态度、实施应对策略和接受支持以良好地生活在痴呆症中的好处。

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