International Summit Consensus Statement: Intellectual Disability Inclusion in National Dementia Plans.
Karen WatchmanMatthew P JanickiMichael SplaineFrode K LarsenTiziano GomieroRonald LucchinoPublished in: American journal of Alzheimer's disease and other dementias (2017)
The World Health Organization (WHO) has called for the development and adoption of national plans or strategies to guide public policy and set goals for services, supports, and research related to dementia. It called for distinct populations to be included within national plans, including adults with intellectual disability (ID). Inclusion of this group is important as having Down's syndrome is a significant risk factor for early-onset dementia. Adults with other ID may have specific needs for dementia-related care that, if unmet, can lead to diminished quality of old age. An International Summit on Intellectual Disability and Dementia, held in Scotland, reviewed the inclusion of ID in national plans and recommended that inclusion goes beyond just description and relevance of ID. Reviews of national plans and reports on dementia show minimal consideration of ID and the challenges that carers face. The Summit recommended that persons with ID, as well as family carers, should be included in consultation processes, and greater advocacy is required from national organizations on behalf of families, with need for an infrastructure in health and social care that supports quality care for dementia.
Keyphrases
- intellectual disability
- quality improvement
- mild cognitive impairment
- healthcare
- autism spectrum disorder
- cognitive impairment
- early onset
- palliative care
- mental health
- health insurance
- public health
- primary care
- systematic review
- affordable care act
- risk assessment
- randomized controlled trial
- pain management
- social media
- health information
- meta analyses