Asia-Pacific Consensus Statement On Dementia
Representatives from twelve national Alzheimer's Associations throughout the Asia-Pacific region convened twice in Singapore to address dementia-related medical and service challenges facing the region. The group focused discussion on issues concerning public awareness, caregiver support, and training of professionals. The representatives agree to construct a brief (not longer than two A4 pages) Consensus Statement which would be useful for each national association. The initial drafts were sent to the designated representative of each association by email or fax. Comments and suggested amendments were repeatedly edited into the document until one version was approved by all. The approved version is presented herein. This document will help to advance dementia-related medical and service activities within the Asia-Pacific region.
CONSENSUS STATEMENT
Background:
By the year 2025, the number of people with dementia in the Asia-Pacific region will more than double. This increase will be much more rapid than that occurring in the West. In 1999 and 2000, two Asia-Pacific Consensus Conferences on Dementia were held in Singapore and were attended by representatives from twelve national Alzheimer's Associations. The goals of these conferences were to elucidate the current regional situation regarding dementia and to reach consensus on plans to address dementia-related medical and service challenges in the region. This document is a consensus statement forged by the twelve regional associations, nine of which are members of Alzheimer's Disease International
Area of
Focus:
The
working group members focused discussion on three critical areas: public
awareness, caregiver support, and training of professionals. Consensus in each
of these areas is described below.
A
fundamental role of Alzheimer's Associations is to work continuously to establish
public awareness and to improve public understanding of dementia. The specific
aims of public awareness and public education activities are to change the
misperception that dementia is part of "normal aging", to alleviate the social
stigma associated with dementia and to dispel the myth that there is neither
practical social support nor effective medical treatment for dementia. If these
aims are successfully achieved, the general public will understand that dementia
is a medical condition and that early detection and accurate diagnosis is
necessary to improve quality of life for people with dementia and their
families.
Aware of dementia must be developed at
many levels and by various means. Dissemination of appropriate information to
the general public can occur via distribution of locally prepared, free, printed
materials such as pamphlets, bookmarks and the like. Positively engaging local and regional
newspaper, radio and television media can also advance awareness. Public
testimonies from affected families, either live or in the form of videotapes and
audiotapes, are additional effective tools for
generating awareness. The success of public awareness and public education efforts can be enhanced
by
coordinating these activities with other organizations involved in the care of
the elderly, and by working collaboratively with other interested healthcare and
social service professionals.
Non-governmental organizations such as national Alzheimer's Associations need to convey to local and national governments relevant factual information about dementia, which can then be incorporated into disease awareness campaigns. Fundraising activities for dementia-related services can also serve as opportunities for building public awareness. Each national association must carefully identify the most appropriate level (e.g., general public, professional organizations, local government) at which to target their public awareness efforts.
Caregiver
Support
Support for caregivers is the foundation
for effective dementia care. The components of caregiver support must include
medical, social, emotional, financial, legal and respite services. These services must be culturally
appropriate, as well as locally available, accessible, affordable, timely and
practical.
Common needs identified by caregivers
of persons with dementia include creating a safe living environment, managing
functional problems such as incontinence, coping with behavioral problems like
agitation, and maintaining family values, family relationships and personal
dignity throughout the course of the disease. In addition, caregivers need to
successfully manage their own stress in order to effectively care for their
afflicted loved one. Practical services which need to be further developed in
many countries of the Asia-Pacific region include caregiver support groups, day
care centres, in-home or visiting nurse services, residential care, respite care
and "how-to" caregiver information which is sensitive to local customs, cultures
and languages.
Training of
Professionals:
Formal education and training
opportunities need to be available for anyone providing care for people with
dementia or their families. Such training may range from credit awarding,
continuing medical education programs for physicians, to workshops or "diploma
course" in dementia care for caregivers. Those providers most likely to be
involved in the early detection of dementia must be identified and trained. Formal instruction on dementia should be
a required part of the curriculum for students in all health and social science
disciplines.
The
training of dementia care providers must include instruction in several relevant
dimensions. A philosophy of care should be taught which emphasizes principles
such as autonomy, inclusiveness and respect for culture diversity. Established
diagnostic criteria and accurate diagnostic methodologies have to be taught.
Early detection of dementia and appropriate therapeutic intervention must be
emphasized. Practical information such as telephone numbers of local support
services, contact information for dementia care specialists and web page
addresses for information on relevant dementing diseases should be
provided.
National Alzheimer's Associations need to
encourage their respective governments to acknowledge the need to train more
specialists in all areas of dementia care. Each association should support the
development of dementia care training and research centres, and must promote the
establishment of dementia care guidelines and standards in their home
country.
Summary:
The twelve national Alzheimer's
Associations who contributed to this Consensus Statement will continue to
network with one another regionally and will continue to share relevant
expertise and practical resources. It is expected that regional consensus on
dementia will evolve in individual member countries and in the Asia-Pacific region
as a whole. It is the hope of the participating members of these two consensus
conferences that this document will provide the inspiration, direction and
practical ideas to further advance the goals of national Alzheimer's
Associations and to further advance dementia-related medical
and service activities within the Asia-Pacific region.
Acknowledgement:
This work was supported by the
Alzheimer's Disease Association,
Singapore.