𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The experience of burnout among home caregivers of patients with dementia: Relations to depression and quality of life

✍ Scribed by M. Takai; M. Takahashi; Y. Iwamitsu; N. Ando; S. Okazaki; K. Nakajima; S. Oishi; H. Miyaoka

Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
158 KB
Volume
49
Category
Article
ISSN
0167-4943

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Dementia patients caregivers quality of
Dementia patients caregivers quality of life: the PIXEL study
✍ Philippe Thomas; Fabrice LallouΓ©; Pierre-Marie Preux; Cyril Hazif-Thomas; Sylvie πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 85 KB πŸ‘ 2 views

## Abstract ## Background Alzheimer's disease and related syndromes have heavy social and human consequences for the patient and his family. Beyond the neuropsychiatric effects of specific therapies for dementia, one of today's challenges is the quality of life for both patients and their informal

The patient with dementia, the caregiver
The patient with dementia, the caregiver and the doctor: cognition, depression and quality of life from three perspectives
✍ SΓΆnke Arlt; Juliane Hornung; M. Eichenlaub; Holger Jahn; Monika Bullinger; Corin πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 126 KB πŸ‘ 2 views

## Abstract ## Background For comprehensive information about the situation of patients with dementia or mild cognitive impairment (MCI), clinicians have to rely on information from different sources, e.g. caregivers or the patients themselves, which may differ from each other. In addition to the