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Needs Detection for Carers of Family Members with Dementia
Oriol Turró-Garriga1,2, Maria Del Mar Fernández-Adarve3, Pilar Monreal-Bosch4,5
1Dementia Registry of Girona (ReDeGi), Institut d'Assistència Sanitària, 17190 Salt, Catalonia, Spain.
Aim:
To determine the perceived needs of carers of non-institutionalized family members that suffer from dementia.
Methods:
Two-steps qualitative study by focus groups of relatives in three centres of different characteristics from the Girona Health Region (step 1) and two in-depth interviews with significant professionals in dementia care (step 2). The analysis was performed based on the interpretation of the transcribed data and the bottom-up coding of categories and themes. The information was triangulated and coding was agreed upon.
Results:
There were three groups, 26 main carers of community-dwelling relatives with dementia in step 1 and two in-depth interviews with dementia-specialised healthcare and social care professionals in step 2. The demands were categorised according to three main themes: whether they were addressed to the members of care services for more direct and close care, to the agencies for a better joint working and less fragmented system, or to society for better comprehension and social recognition. We emphasize the need for a consultation-liaison reference figure throughout the process both for aspects of greater efficiency in the management of resources and for greater empowerment of carers.
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