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Perspectives on family caregiving of people aging with intellectual disability affected by dementia: Commentary from the International Summit on Intellectual Disability and Dementia
N. Jokinen, T. Gomiero, K. Watchman, MP. Janicki, M. Hogan, F. Larsen, A. Beránková, F. Heloísa Santos, K. Service, J. Crowe,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, Research Support, U.S. Gov't, P.H.S.
Odkazy
PubMed
29583104
DOI
10.1080/01634372.2018.1454563
Knihovny.cz E-zdroje
- MeSH
- demence komplikace psychologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mentální retardace komplikace psychologie MeSH
- osoby pečující o pacienty psychologie MeSH
- senioři MeSH
- zdravotní politika MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
This article, an output of the 2016 International Summit on Intellectual Disability and Dementia, examines familial caregiving situations within the context of a support-staging model for adults with intellectual disability (ID) affected by dementia. Seven narratives offer context to this support-staging model to interpret situations experienced by caregivers. The multidimensional model has two fundamental aspects: identifying the role and nature of caregiving as either primary (direct) or secondary (supportive); and defining how caregiving is influenced by stage of dementia. We propose staging can affect caregiving via different expressions: (1) the "diagnostic phase," (2) the "explorative phase," (3) the "adaptive phase," and (4) the "closure phase." The international narratives illustrate direct and indirect caregiving with commonality being extent of caregiver involvement and attention to the needs of an adult with ID. We conclude that the model is the first to empirically formalize the variability of caregiving within families of people with ID that is distinct from other caregiving groups, and that many of these caregivers have idiosyncratic needs. A support-staging model that recognizes the changing roles and demands of carers of people with ID and dementia can be useful in constructing research, defining family-based support services, and setting public policy.
b Project DAD ANFFAS Trentino Onlus Trento Italy
c Faculty of Health Sciences and Sport University of Stirling Scotland
Department of Disability and Human Development University of Illinois at Chicago USA
e National Task Group in Intellectual Disabilities and Dementia Practices Eliot ME USA
f Norwegian National Advisory Unit on Ageing and Health Oslo Norway
g Centre of Expertise in Longevity and Long term Care Charles University Prague Czech Republic
j Nurse Practitioner Consultant Northampton MA USA
School of Social Work University of Northern British Columbia Prince George Canada
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