Family quality of life in dementia: a qualitative approach to family-identified care priorities
Author:
Publisher
Springer Science and Business Media LLC
Subject
Public Health, Environmental and Occupational Health
Link
http://link.springer.com/content/pdf/10.1007/s11136-011-9852-4.pdf
Reference13 articles.
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2. Jonsson, L., Andreasen, N., Kilander, L., et al. (2006). Patient- and proxy-reported utility in Alzheimer’s disease using the EuroQoL. Alzheimer Disease and Associated Disorders, 20, 49–55.
3. Karlawish, J. H., Zbrozek, A., Kinosian, B., Gregory, A., Ferguson, A., Low, D. V., et al. (2008). Caregivers’ assessments of preference-based quality of life in Alzheimer’s disease. Alzheimer’s & Dementia, 4, 203–211.
4. Neumann, P. J. (2005). Health utilities in Alzheimer’s disease and implications for cost-effectiveness analysis. Pharmacoeconomics, 23, 437–541.
5. Park, J., Hoffman, L., Marquis, J., Turnbull, L., Poston, D. J., Marquis, J., et al. (2003). Toward assessing family outcomes of service delivery: Validation of a family quality of life survey. Journal of Intellectual Disability Research, 47, 367–384.
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