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Dependency and Community Care in Presenile Alzheimer's Disease

Published online by Cambridge University Press:  02 January 2018

Andrew J. Newens*
Affiliation:
Centre for Health Services Research, University of Newcastle upon Tyne
Donald P. Forster
Affiliation:
School of Health Care Sciences, University of Newcastle upon Tyne
David W. K. Kay
Affiliation:
MRC Neurochemical Pathology Unit, Newcastle General Hospital, Newcastle upon Tyne
*
Dr Newens, University of Newcastle upon Tyne, Centre for Health Services Research, 21 Claremont Road, Newcastle upon Tyne NE2 4AA

Extract

Background

In a study of patients with presenile dementia of Alzheimer type (PDAT), we aimed to investigate functional dependency in relation to the time since diagnosis and place of residence. Use of community and support services and the time between diagnosis and entry to permanent residential care were also studied.

Method

Interviews with 109 cases of PDAT (diagnosed before age 65) and their carers.

Results

The need for assistance in activities of daily living (ADL) was progressive with time from diagnosis. Five years after diagnosis, 57% of patients remained at home, 20% of whom required some assistance in each of six areas of ADL. The need for assistance in each ADL category was significantly greater for cases in permanent residential care than for those at home. There were no significant differences between the Mini-Mental State Examination (MMSE) scores of patients at home and those of patients in permanent care. Incontinence and the relationship of the carer to the patient were the strongest predictors of permanent residential care. Respite care had been offered in 63% of cases; 71% of these offers had been accepted.

Conclusions

Patients with PDAT who have a living relative are cared for at home for a considerable period of time despite severe cognitive impairment and loss of independence measured by ADL. The reports of carers suggest there is scope for improvement in supportive services to meet this community need.

Type
Papers
Copyright
Copyright © Royal College of Psychiatrists, 1995 

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References

American Psychiatric Association (1987) Diagnostic and Statistical Manual of Mental Disorders (3rd edn, revised) (DSM–III–R). Washington, DC: APA.Google Scholar
Barnes, R. F., Raskind, M. A., Scott, M., et al (1981) Problems of families caring for Alzheimer's patients: use of a support group. Journal of the American Geriatrics Society, 29, 8085.CrossRefGoogle ScholarPubMed
Berkson, J. & Gage, R. (1950) Calculation of survival rates for cancer. Proceedings of the Mayo Clinic, 25, 270.Google Scholar
Blessed, G., Tomlinson, B. E. & Roth, M. (1968) The association between quantitative measures of dementia and of senile change in cerebral grey matter of elderly subjects. British Journal of Psychiatry, 114, 797811.Google Scholar
Chenoweth, B. & Spencer, B. (1986) Dementia: the experience of family caregivers. The Gerontologist, 26, 267272.Google Scholar
Colerick, E. J. & George, L. K. (1986) Predictors of institutionalisation among caregivers of patients with Alzheimer's disease. Journal of the American Geriatrics Society, 34, 493498.Google Scholar
Copeland, J. R. M. & Dewey, M. E. (1991) Neuropsychological diagnosis (GMS-HAS-AGECAT package). International Psychogeriatrics, 3 (suppl.), 4349.CrossRefGoogle Scholar
Department of Health and Social Security (1989) Caring for People. London: HMSO.Google Scholar
Eagles, J. M., Craig, A., Rawlinson, F., et al (1987) The psychological well being of supporters of the demented elderly. British Journal of Psychiatry, 150, 293298.CrossRefGoogle ScholarPubMed
Folstein, M. F., Folstein, S. & McHugh, P. (1975) Mini-Mental State, a practical method for grading the cognitive state of patients for the clinician. Journal of Psychiatric Research, 12, 189198.Google Scholar
Furst, M. & Sperlinger, D. (1992) Hour to Hour, Day to Day. A Survey of the Service Experiences of People with Presenile Dementia in the London Borough of Sutton. Sutton, Surrey: St Helier NHS Trust.Google Scholar
George, L. & Gwyther, L. (1986) Caregiver well-being: a multidimensional examination of family caregivers of demented adults. The Gerontologist, 26, 253259.Google Scholar
Gilhooly, M. L. M. (1984) The impact of caregiving on caregivers. British Journal of Medical Psychology, 57, 3344.Google Scholar
Gilleard, C. J. (1984) Problems posed for supporting relatives of geriatric and psychogeriatric day patients. Acta Psychiatra Scandinavica, 70, 198208.Google Scholar
Gilleard, C. J. (1987) Influence of emotional distress among supporters on the outcome of psychogeriatric day care. British Journal of Psychiatry, 150, 219223.Google Scholar
Greene, J. G., Smith, R., Gardiner, M., et al (1982) Measuring behavioural disturbance of elderly demented patients in the community and its effects on relatives: a factor analytic study. Age and Ageing, 11, 121126.Google Scholar
Illing, J., Drinkwater, C. & Rogerson, T. (1990) Evaluation of community psychiatric nursing in general practice. In Community Psychiatric Nursing: A Research Perspective (ed. Brooker, C.), pp. 144173. London: Chapman & Hall.Google Scholar
Katz, S., Ford, A. B., Moskowitz, R. W., et al (1963) The index of ADL: a standardised measure of biological and psychosocial functioning. Journal of the American Medical Association, 9, 9499.Google Scholar
Lee, L. & Desu, M. (1972) A computer program for comparing K samples with right-censored data. Computer Programs in Biomedicine, 2, 315321.Google Scholar
McKhann, G., Drachman, D., Folstein, M., et al (1984) Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA work group under the auspices of Department of Health and Human Services Task Force on Alzheimer's disease. Neurology, 34, 939944.CrossRefGoogle ScholarPubMed
Melzer, D. (1990) An evaluation of a respite care unit for elderly people with dementia: framework and some results. Health Trends, 22, 6467.Google Scholar
Newens, A. J., Forster, D. P., Kay, D. W. K., et al (1993a) Clinically diagnosed presenile dementia of the Alzheimer type in the Northern health region: ascertainment, prevalence, incidence and survival. Psychological Medicine, 23, 631644.Google Scholar
Newens, A. J., Forster, D. P. & Kay, D. W. K. (1993b) Death certification after a diagnosis of presenile dementia. Journal of Epidemiology and Community Health, 47, 293297.Google Scholar
O'Connor, D. W., Pollitt, P. A., Roth, M., et al (1990) Problems reported by relatives in a community study of dementia. British Journal of Psychiatry, 156, 835841.Google Scholar
Whittick, J. E. (1988) Dementia and mental handicap: emotional distress in carers. British Journal of Clinical Psychology, 27, 167172.CrossRefGoogle ScholarPubMed
Zarit, S. H., Reever, K. E. & Bach Peterson, J. (1980) Relatives of the impaired elderly, correlates of feelings of burden. The Gerontologist, 20, 649655.Google Scholar
Zarit, S. H., Todd, P. A. & Zarit, J. M. (1986) Subjective burden of husbands and wives as caregivers: a longitudinal study. The Gerontologist, 26, 260266.Google Scholar
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