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Users may use the search function to find links to journals, books, policy papers and surveys and databases related to dementia in the Republic of Ireland and Northern Ireland. Users can search by keyword or theme and then use filters to refine results by content type, year and themes.

Focus on Dementia

CARDI
CARDI
2010

In 2010, CARDI provided an update on policy around dementia in ROI and NI, at a time that commitments had been made to developing national dementia strategies in both jurisdictions.

The briefing paper also drew attention to the relatively low level of funding for research on dementia in comparison to other chronic conditions and makes the case for the promised national dementia strategies in ROI and NI to be used as channels for promoting research on dementia, as has been done in other countries.    

Medication use in patients with dementia at the end of life

CARDI
CARDI
2012

This Research presents a summary of the findings of a project entitled Assessment of factors which influence physician decision-making regarding medication use in patients with dementia at the end of life (Parsons, et al., 2012). The project was undertaken in both ROI and NI.

Key findings are that there is considerable variability in decision-making among NI and ROI doctors about continuation or discontinuation of some medications at the end of life in patients with dementia, especially in relation to antibiotics, and dementia medications. The research showed that the presence of an advance directive did not necessarily have an effect on doctor decision-making regarding medications. The findings highlight the importance of clinical practice guidelines as a tool for helping doctors make decisions on the prescription of medications such as statins and anti-psychotics for people with dementia and the absence of such guidelines at the time in ROI (although clinical practice guidelines for general practitioners have since been introduced in ROI).  A conclusion drawn is that the wishes and comfort of the person with dementia and the person’s family should be at the forefront of decision making when it comes to end of life care in dementia.