'It's definitely not Alzheimer's': Perceived benefits and drawbacks of a mild cognitive impairment diagnosis.

GOMERSALL, Tim, SMITH, Sarah Kate, BLEWETT, Charlotte and ASTELL, Arlene (2017). 'It's definitely not Alzheimer's': Perceived benefits and drawbacks of a mild cognitive impairment diagnosis. British Journal of Health Psychology, 22 (4), 786-804.

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Official URL: https://bpspsychub.onlinelibrary.wiley.com/doi/10....
Link to published version:: https://doi.org/10.1111/bjhp.12255
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    Abstract

    Objectives To understand the perceived benefits and drawbacks of a mild cognitive impairment (MCI) diagnosis from the perspective of those living with the label. Methods Participants were included if they had recently (within 6 months) received a MCI diagnosis. We also recruited close family members to gain their perspectives. Each was interviewed separately with a semi-structured topic guide covering three areas: (1) experience of cognitive impairments and changes in the individual; (2) impact of cognitive impairment(s) on daily activities and social relationships; and (3) experience of the diagnosis process and living with the label. Transcribed interviews were stored in Nvivo®. Grounded theory procedures of memo writing, open coding, constant comparison, and focused coding were used to derive conceptual themes. Results Eighteen dyads were interviewed. The overarching themes surrounding diagnosis benefits and drawbacks were as follows: (1) emotional impact of the diagnosis; (2) practical benefits and limitations of the diagnosis, in terms of (a) understanding one's symptoms and (b) access to clinical support. Although participants were glad to have clinical support in place, they expressed frustration at the lack of clarity, and the lack of available treatments for MCI. Consequently, living with MCI can be characterized as an ambivalent experience. Conclusion As a clinical label, MCI appears to have little explanatory power for people living with cognitive difficulties. Work is needed to clarify how clinicians and patients communicate about MCI, and how people can be helped to live well with the label. Despite an emerging body of prognostic studies, people with MCI are likely to continue living with significant uncertainty.

    Item Type: Article
    Uncontrolled Keywords: ageing; diagnosis; grounded theory; illness experiences; illness perceptions; memory; mild cognitive disorder; mild cognitive impairment; neurocognitive illness; qualitative research; semi-structured interviews; Aged; Aged, 80 and over; Alzheimer Disease; Anxiety; Cognitive Dysfunction; Diagnosis, Differential; Family; Female; Humans; Interviews as Topic; Male; Middle Aged; Qualitative Research; Humans; Alzheimer Disease; Diagnosis, Differential; Anxiety; Family; Qualitative Research; Aged; Aged, 80 and over; Middle Aged; Female; Male; Interviews as Topic; Cognitive Dysfunction; 1117 Public Health and Health Services; 1608 Sociology; 1701 Psychology; Clinical Psychology
    Identification Number: https://doi.org/10.1111/bjhp.12255
    Page Range: 786-804
    SWORD Depositor: Symplectic Elements
    Depositing User: Symplectic Elements
    Date Deposited: 08 Dec 2021 11:37
    Last Modified: 04 Jan 2022 12:24
    URI: http://shura.shu.ac.uk/id/eprint/29021

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