Kavanagh, Shane M. and Opit, Louis J. (1999) The prevalence and balance of care for people with intellectual disability: secondary analyses of the OPCS disability surveys. Journal of Applied Research in Intellectual Disabilities, 12 (2). pp. 127-148. ISSN 1360-2322. (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided)
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Government policy continues to emphasise the commissioning and needs-assessment role of health authorities, local<p><p>authorities and - to a greater extent - general practitioners. To date, much available information for this purpose has been based on service utilisation data or from registers based on case finding from service contacts. As an alternative, we conducted secondary analyses of the national Surveys of Disability of Children and Adults by the Office of Population Census and Surveys. The prevalence of intellectual disability for people who had 'mental handicap' reported as an underlying health problem was 3.5 per 1000 in the overall population. Rates rose from 1.7 per 1000 among those aged 4 and under, reaching a peak of 6.3 per 1000 among 16 - 19 year olds and falling to 2.8 per 1000 among people aged 75 or more. Residence in a communal establishment increased markedly with age. People in households had high levels of disability and consequently problems with personal care. Furthermore, behaviour problems were commonplace. Consequently, carers spent long hours caring and often reported adverse effects on their health.
|Divisions:||Faculties > Social Sciences > School of Social Policy Sociology and Social Research > Personal Social Services Research Unit|
|Depositing User:||Rosalyn Bass|
|Date Deposited:||20 May 2011 14:42|
|Last Modified:||23 Jun 2014 07:58|
|Resource URI:||https://kar.kent.ac.uk/id/eprint/26865 (The current URI for this page, for reference purposes)|