Caregiver burden outcomes
Brodaty, Henry, and Thompson, Claire (2006) Caregiver burden outcomes. In: Rockwood, Kenneth, and Gauthier, Serge, (eds.) Trial Designs and Outcomes in Dementia Therapeutic Research. CRC Press, Boca Raton, FL, USA, pp. 141-152.
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Abstract
Most people with dementia live at home with their family, friends or another person who assists them in managing day to day life. In the USA approximately 49% of these caregivers are spouses of the patient, 45% are children, 77% are women and 73% are over 50 years of age.
The responsibility or 'burden' of caring for a person with dementia is immense, and it has become common to refer to the caregiver as a second patient. The time demands of caregiving for a person with dementia have been referred to as the '36 hour day'. Estimates range from 50 to 286 hours per month, with time demands increasing as the illness progresses.
| Item ID: | 29129 | 
|---|---|
| Item Type: | Book Chapter (Research - B1) | 
| ISBN: | 978-0-203-34065-3 | 
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| Date Deposited: | 04 Jun 2014 05:40 | 
| FoR Codes: | 11 MEDICAL AND HEALTH SCIENCES > 1117 Public Health and Health Services > 111714 Mental Health @ 50% 17 PSYCHOLOGY AND COGNITIVE SCIENCES > 1701 Psychology > 170101 Biological Psychology (Neuropsychology, Psychopharmacology, Physiological Psychology) @ 50% | 
| SEO Codes: | 97 EXPANDING KNOWLEDGE > 970111 Expanding Knowledge in the Medical and Health Sciences @ 50% 97 EXPANDING KNOWLEDGE > 970117 Expanding Knowledge in Psychology and Cognitive Sciences @ 50% | 
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