Acceptability and use of a patient-held communication tool for people living with dementia: a longitudinal qualitative study

被引:2
|
作者
Leavey, Gerard [1 ,2 ]
Corry, Dagmar Suzanna [1 ,2 ]
Waterhouse-Bradley, Bethany [3 ]
Curran, Emma [2 ]
Todd, Stephen [4 ]
McIlfatrick, Sonja [5 ]
Coates, Vivien [6 ]
Watson, Max [5 ]
Abbott, Aine [7 ]
McCrory, Bernadine [8 ]
McCormack, Brendan [9 ]
机构
[1] Ulster Univ, Psychol, Coleraine, Londonderry, North Ireland
[2] Ulster Univ, Bamford Ctr Mental Hlth & Wellbeing, Coleraine Campus, Coleraine, Londonderry, North Ireland
[3] Ulster Univ, Social Policy, Belfast, Antrim, North Ireland
[4] Altnagelvin Hosp Hlth & Social Serv Trust, Geriatr, Coleraine, Londonderry, North Ireland
[5] Ulster Univ, Nursing & Hlth Sci, Belfast, Antrim, North Ireland
[6] Ulster Univ, Dept Nursing & Hlth Sci, Coleraine Campus, Coleraine, Londonderry, North Ireland
[7] Western Hlth & Social Care NHS Trust, Integrated Care Clin, Derry, North Ireland
[8] Alzheimers Soc Northern Ireland, Belfast, Antrim, North Ireland
[9] Queen Margaret Univ, Ctr Person Ctr Practice Res, Edinburgh, Midlothian, Scotland
来源
BMJ OPEN | 2020年 / 10卷 / 05期
关键词
caregivers; communication; dementia; information; patient-held records;
D O I
10.1136/bmjopen-2019-036249
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives To assess the acceptability and use of a low-cost patient-held communication tool. Design Longitudinal qualitative interviews at three time points over 18 months and document content analysis. Setting Primary and community services. Participants Twenty-eight dyads: People living with dementia in Northern Ireland and their informal carers. Interventions A patient-held healthcare 'passport' for people living with dementia. Primary and secondary outcomes Acceptability and use of the passport-barriers and facilitators to successful engagement. Results There was a qualified appreciation of the healthcare passport and a much more nuanced, individualistic or personalised approach to its desirability and use. How people perceive it and what they actually do with it are strongly determined by individual contexts, dementia stage and other health problems, social and family needs and capacities. We noted concerns about privacy and ambivalence about engaging with health professionals. Conclusion Such tools may be of use but there is a need for demanding, thoughtful and nuanced programme delivery for future implementation in dementia care. The incentivisation and commitment of general practitioners is crucial. Altering the asymmetrical relationship between professionals and patients requires more extensive attention.
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页数:9
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