Access the full text.
Sign up today, get DeepDyve free for 14 days.
L. Annerstedt, S. Elmståhl, B. Ingvad, S. Samuelsson (2000)
Family caregiving in dementiaScandinavian Journal of Public Health, 28
M. Liken, S. King (1995)
Home Health Aide Service: Barriers Perceived by Dementia Family CaregiversHome Healthcare Nurse: The Journal for the Home Care and Hospice Professional, 13
C. Farran, D. Loukissa, S. Perraud, Olimpia Paun (2004)
Alzheimer's disease caregiving information and skills. Part II: family caregiver issues and concerns.Research in nursing & health, 27 1
S. Zarit, J. Gaugler, S. Jarrott (1999)
Useful services for families: research findings and directionsInternational Journal of Geriatric Psychiatry, 14
M. Ory, Richard Hoffman, Jennifer Yee, S. Tennstedt, R. Schulz (1999)
Prevalence and impact of caregiving: a detailed comparison between dementia and nondementia caregivers.The Gerontologist, 39 2
H. Arksey, C. Glendinning (2006)
Choice in the context of informal care-giving.Health & social care in the community, 15 2
J. Leon, Peter Neumann, R. Hermann, M. Hsu, J. Cummings, P. Doraiswamy, D. Marin (2000)
Health-related quality-of-life and service utilization in Alzheimer's disease: A cross-sectional studyAmerican Journal of Alzheimer's Disease and Other Dementias, 15
C. Thompson, K. Spilsbury (1998)
Support for carers of people with Alzheimer's type dementia.The Cochrane database of systematic reviews, 2
Emma Gruffydd, J. Randle (2006)
Alzheimer's disease and the psychosocial burden for caregivers.Community practitioner : the journal of the Community Practitioners' & Health Visitors' Association, 79 1
M. Harrison, A. Neufeld (1997)
Women's experiences of barriers to support while caregiving.Health care for women international, 18 6
J. Ritchie, L. Spencer (2002)
Qualitative data analysis for applied policy research
G. Luscombe, H. Brodaty, S. Freeth (1998)
Younger people with dementia: diagnostic issues, effects on carers and use of servicesInternational Journal of Geriatric Psychiatry, 13
P. Lane, H. McKenna, A. Ryan, P. Fleming (2003)
The Experience of the Family Caregivers’ Role: A Qualitative StudyResearch and Theory for Nursing Practice, 17
K. Sullivan, F. O'Conor (2001)
Providing education about Alzheimer's diseaseAging & Mental Health, 5
J. Millán-Calenti, Manuel Gandoy-Crego, M. Antelo-Martelo, M. López-Martínez, M. Riveiro-López, J. Mayán-Santos (2000)
Helping the family carers of Alzheimer's patients: from theory...to practice. A preliminary study.Archives of gerontology and geriatrics, 30 2
H. Arksey (2003)
Scoping the field: services for carers of people with mental health problems.Health & social care in the community, 11 4
H. Brodaty, D. Hadzi-Pavlovic (1990)
Psychosocial Effects on Carers of Living with Persons with DementiaAustralian and New Zealand Journal of Psychiatry, 24
C. Farran, D. Loukissa, S. Perraud, Olimpia Paun (2003)
Alzheimer's disease caregiving information and skills. Part I: care recipient issues and concerns.Research in nursing & health, 26 5
M. Buono, Renata Busato, M. Mazzetto, Bruno Paccagnella, Federica Aleotti, O. Zanetti, A. Bianchetti, M. Trabucchi, D. Leo (1999)
Community care for patients with Alzheimer's disease and non‐demented elderly people: use and satisfaction with services and unmet needs in family caregiversInternational Journal of Geriatric Psychiatry, 14
E. McCarty, C. Drebing (2003)
Exploring professional caregivers' perceptions. Balancing self-care with care for patients with Alzheimer's disease.Journal of gerontological nursing, 29 9
H. Brodaty, A. Green (2002)
Who cares for the carer? The often forgotten patient.Australian family physician, 31 9
B. Winslow (2003)
Family caregivers' experiences with community services: a qualitative analysis.Public health nursing, 20 5
R. Hunter, L. McGill, N. Bosanquet, Johnson Research, Dr Johnson, Cambridge Pharma, Consultancy (1997)
Alzheimer's disease in the United Kingdom: developing patient and carer support strategies to encourage care in the community.Quality in Health Care, 6
L. Dorfman, K. Berlin, C. Holmes (1998)
Attitudes toward service use among wife caregivers of frail older veterans.Social work in health care, 27 4
This study investigated, by way of interview (n=45), the needs of those caring for a person with dementia and their satisfaction with current services in the Caerphilly County Borough of South Wales. Carers reported having the most difficulty coping with the demands on their time and the emotional strain associated with caring. Carers requested more information regarding available services, the diagnosis of dementia and the legal and financial aspects of caring. They also mentioned the need for a night‐sitter service, a 24‐hour helpline, more support groups and more visits from social workers and community psychiatric nurses (CPNs). On the whole, the carers were satisfied with the services provided, although their use of these services was not extensive. However, issues around lack of support, quality and availability of homes and hospitals and poor communications were identified as areas of concern. The findings were welcomed by strategic planners and the information is being used as a basis for developing and improving specific carer support services.
Quality in Ageing and Older Adults – Emerald Publishing
Published: Jun 1, 2008
Keywords: Alzheimer's disease; Dementia; Carer; Service; Needs; Service developments
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.