How do people living with dementia perceive eating and drinking difficulties? A qualitative study

Author:

Anantapong Kanthee12,Barrado-Martín Yolanda3,Nair Pushpa3,Rait Greta3,Smith Christina H4,Moore Kirsten J15,Manthorpe Jill6,Sampson Elizabeth L17,Davies Nathan13

Affiliation:

1. Marie Curie Palliative Care Research Department, Division of Psychiatry, University College London, London, UK

2. Department of Psychiatry, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand

3. Centre for Ageing Population Studies, Research Department of Primary Care and Population Health, University College London, London, UK

4. Language and Cognition, Division of Psychology and Language Sciences, University College London, London, UK

5. National Ageing Research Institute, Parkville, Victoria, Australia

6. NIHR Policy Research Unit in Health & Social Care Workforce and NIHR Applied Research Collaborative (ARC) South London, King's College London, London, UK

7. Barnet Enfield and Haringey Mental Health Trust Liaison Team, North Middlesex University Hospital, Sterling Way, London, UK

Abstract

Abstract Background Eating and drinking problems are common among people living with later-stage dementia, yet few studies have explored their perspectives. Objective This study aimed to explore how people living with mild dementia understand possible future eating and drinking problems and their perspectives on assistance. Design Qualitative study using semi-structured interviews. Setting Community. Methods We conducted semi-structured interviews with 19 people living with mild dementia. Interviews were transcribed verbatim and analysed thematically. Results Five themes were identified: (i) awareness of eating and drinking problems; (ii) food and drink representing an individual’s identity and agency; (iii) delegating later decisions about eating and drinking to family carers; (iv) acceptability of eating and drinking options; and (v) eating and drinking towards the end of life. For people living with mild dementia, possible later eating and drinking problems could feel irrelevant and action may be postponed until they occur. Fears of being a burden to family and of being treated like a child may explain reluctance to discuss such future problems. People living with mild dementia might wish to preserve their agency and maintain good quality of life, rather than be kept alive at later stages by artificial nutrition and hydration. Conclusion For people with mild dementia, eating and drinking problems may seem unrelated to them and so get left undiscussed. Negative connotations regarding eating and drinking problems may hinder the discussion. The optimal time to discuss possible future problems with eating and drinking with people with mild dementia may need an individual approach.

Funder

Marie Curie

Publisher

Oxford University Press (OUP)

Subject

Geriatrics and Gerontology,Ageing,General Medicine

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