| Literature DB >> 30595033 |
Uwe Konerding1,2, Tom Bowen3, Paul Forte3, Eleftheria Karampli4, Tomi Malmström5, Elpida Pavi4, Paulus Torkki5, Elmar Graessel6.
Abstract
The relationships between caregiver burden as measured with the Burden Scale for Family Caregivers-short form and 6 characteristics of caregivers caring for patients with dementia were investigated for caregivers from England (n = 36), Finland (n = 42), and Greece (n = 46) using survey data. In all 3 countries, caregiver burden increases with physical problems of the caregiver, emotional problems of the caregiver, and weekly hours of care. Hence, in all 3 countries, special support for informal care is required when these characteristics are at high levels. When the caregiver is a spouse or long-term partner of the person with dementia, lives in the same house as this person, or spends fewer than 20 h/wk for other duties than care, this is associated with less caregiver burden in England but with more caregiver burden in Greece. Accordingly, special support is required for Greek caregivers with these characteristics, but the opposite is true for English caregivers.Entities:
Keywords: caregiver burden; cross-cultural; cross-national; dementia; informal care; informal caregivers
Mesh:
Year: 2018 PMID: 30595033 DOI: 10.1177/1533317518822047
Source DB: PubMed Journal: Am J Alzheimers Dis Other Demen ISSN: 1533-3175 Impact factor: 2.035