Literature DB >> 24284179

Exploring the experiences of people with mild cognitive impairment and their caregivers with particular reference to healthcare - a qualitative study.

Katherine Dean1, Crispin Jenkinson2, Gordon Wilcock3, Zuzana Walker4.   

Abstract

BACKGROUND: The aim of this study was to investigate the experiences of people with mild cognitive impairment (MCI; PWMCI) and their "advocates," particularly within healthcare services.
METHODS: Semi-structured interviews were conducted with 23 PWMCI diagnosed ≤6 months ago and 20 advocates recruited via patients. The resulting data were content-analyzed.
RESULTS: PWMCI interviewed rarely reported negative impressions of their general practitioner (GP). Reports regarding memory services were more mixed: positive impressions related to finding the service to be "well run" and the staff "pleasant," negative ones to the assessment process or a perceived lack of feedback. Aside from improved information provision, most PWMCI had no suggestions for improvements to their healthcare. However, these results should be interpreted with caution as many of the PWMCI interviewed displayed evidence of impaired recall and/or insight relating to their condition and healthcare. Advocates generally reported more negative impressions of both contact with the PWMCI's GP (most commonly reporting a "dismissive" attitude) and memory services (with common complaints relating to the assessments used in clinics and lengthy waiting times). This group generally had suggestions for improvements to services - particularly regarding information provision, changes in the assessment process, and improvements in communication by services.
CONCLUSIONS: To our knowledge, this is the first in-depth study of the difficulties experienced by PWMCI and their advocates which includes the context of healthcare provision. The specific needs of these groups, as described here, as well as those of people with dementia, should be considered when designing memory clinics and other related services.

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Mesh:

Year:  2013        PMID: 24284179     DOI: 10.1017/S104161021300207X

Source DB:  PubMed          Journal:  Int Psychogeriatr        ISSN: 1041-6102            Impact factor:   3.878


  5 in total

1.  Factors Influencing Emergency Care by Persons With Dementia: Stakeholder Perceptions and Unmet Needs.

Authors:  Gwen Costa Jacobsohn; Matthew Hollander; Aaron P Beck; Andrea Gilmore-Bykovskyi; Nicole Werner; Manish N Shah
Journal:  J Am Geriatr Soc       Date:  2019-01-09       Impact factor: 5.562

2.  In the Information Age, do dementia caregivers get the information they need? Semi-structured interviews to determine informal caregivers' education needs, barriers, and preferences.

Authors:  Kendra Peterson; Howard Hahn; Amber J Lee; Catherine A Madison; Alireza Atri
Journal:  BMC Geriatr       Date:  2016-09-23       Impact factor: 3.921

3.  What outcomes are important to patients with mild cognitive impairment or Alzheimer's disease, their caregivers, and health-care professionals? A systematic review.

Authors:  Claire Tochel; Michael Smith; Helen Baldwin; Anders Gustavsson; Amanda Ly; Christin Bexelius; Mia Nelson; Christophe Bintener; Enrico Fantoni; Josep Garre-Olmo; Olin Janssen; Christoph Jindra; Isabella F Jørgensen; Alex McKeown; Buket Öztürk; Anna Ponjoan; Michele H Potashman; Catherine Reed; Emilse Roncancio-Diaz; Stephanie Vos; Cathie Sudlow
Journal:  Alzheimers Dement (Amst)       Date:  2019-03-07

4.  Conditions required to ensure successful detection and management of mild cognitive impairment in primary care: A Delphi consultation study in China.

Authors:  Yuan Lu; Chaojie Liu; Dehua Yu; Yvonne Wells
Journal:  Front Public Health       Date:  2022-09-23

5.  Features of primary care practice influence emergency care-seeking behaviors by caregivers of persons with dementia: A multiple-perspective qualitative study.

Authors:  Aaron P Beck; Gwen C Jacobsohn; Matthew Hollander; Andrea Gilmore-Bykovskyi; Nicole Werner; Manish N Shah
Journal:  Dementia (London)       Date:  2020-02-12
  5 in total

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