Search:
Browse
Collection All
bullet
bullet
bullet
bullet
bullet
Listed communities
bullet
bullet
HSE
bullet
bullet
LIS
bullet
bullet
bullet

Irish Health Repository > Other Irish Health Organisations > Charitable & Advocacy Organisations > Alzheimer Society of Ireland > Opening conversations Developing a model for The Alzheimer Society of Ireland Developing a model for The Alzheimer Society of Ireland of best-practice palliative care interventions for people with dementia and their carers

Files in This Item:
File Description Size Format View/Open
OpeningConversations.pdf1135KbAdobe PDFThumbnail
View/Open

Title: Opening conversations Developing a model for The Alzheimer Society of Ireland Developing a model for The Alzheimer Society of Ireland of best-practice palliative care interventions for people with dementia and their carers
Authors: MacConville, Úna Dr.
Affiliation: Centre for Death and Society,University of Bath, Bath, UK.
Publisher: Alzheimer Society of Ireland
Issue Date: 2011
URI: http://hdl.handle.net/10147/212749
Additional Links: http://www.alzheimer.ie/
Type: Report
Language: en
Description: Palliative care and end-of-life issues for people with dementia are pertinent areas for research, policy and practice in dementia care. The Alzheimer Society of Ireland (ASI) is the national leader in understanding and providing dementia-specific supports and services, including the development of palliative care for people with dementia. ‘Opening Conversations’ was a small-scale qualitative research project aimed at developing a model of best-practice palliative care interventions for people with dementia in order to integrate palliative care interventions into ASI service planning. It also aimed to deepen an understanding of what palliative care means within the context of dementia care, as well as understanding the specific end-of-life issues for people with dementia, their carers and ASI and other service providers. This research proposes a model of dementia palliative care based on the understanding that the provision of good-quality end-of-life care for people with dementia and their families begins at the time of diagnosis and is not confined to the end stage of the illness or to the period in which the person with dementia is actively dying. A number of research activities were developed on the basis of key issues identified by service managers and team members. Liaison meetings were ongoing throughout the research, incorporating ongoing reflective practice, evaluation and review. Research activities included conversations with people with dementia and family members and carers about end-of-life care; conversations with long-term service providers about the transition to long-term care; a review of ASI information provision, both current and future; and a survey of ASI staff regarding the end-of-life/palliative care issues.
Keywords: PALLIATIVE CARE
DEATH, DISEASE AND DISABILITY
DEMENTIA
CARER
ALZHEIMER'S DISEASE
Appears in Collections: Alzheimer Society of Ireland

Please use this identifier to cite or link to this item: http://hdl.handle.net/10147/212749
    Del.icio.us     LinkedIn     Citeulike     Connotea     Facebook     Stumble it!



All Items in LENUS are protected by copyright, with all rights reserved, unless otherwise indicated.