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Medical Research Council Cognitive Function and Ageing Study (MRC CFAS) and Resource Implications Study (RIS MRC CFAS) Correspondence to: Dr Melzer
dm214{at}medschl.cam.ac.uk
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Abstract |
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Objectives:
To provide estimates of the numbers of
cognitively impaired and physically disabled elderly people in England
and Wales, subdivided by a range of sociodemographic, dependency, care
receipt, and survival variables, to support debates on the form and
funding of health and welfare programmes.
Design:
Interviews at baseline and 2 year follow up plus data on resource use extracted from records for those with disability.
Subjects:
10 377 people aged 65 years and over in
Cambridgeshire, Newcastle, Nottingham, and Oxford. All estimates
weighted to population of England and Wales in 1996.
Results:
11% of men and 19% of women aged 65 and
over were disabled, totalling 1.3 million people; 38% of these were aged 85 or over and a similar percentage were cognitively impaired. Overall, more than 80% of elderly disabled people needed help on at
least a daily basis. Over a third of people with limitations to daily
activity living in private households were wholly or partly dependent
on formal services for help. 63% of disabled elderly people used acute
hospitals during the 2 year follow up, 43% as inpatients. 53% of
those with cognitive impairment and limitations to daily activity were
living in institutions.
Conclusions:
Very elderly people and those with
cognitive impairment make up a large proportion of those in need of
long term care. A large proportion of even the most disabled elderly people currently live outside institutions and depend on formal services as well as informal care givers. Disabled elderly people use
acute hospitals extensively, underlining the interrelations between
acute and long term care.
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Key messages
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Introduction |
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With the historic rise in life expectancy during this century, the human life span is now divided into four ages: the first is an age of dependency, childhood, and education, the second is an age of independence, maturity, and responsibility, and although the third age is considered a period of fulfilment for physically and mentally fit people in retirement, the fourth age is associated with disability and dependence.1 The size and pattern of the fourth age is of critical importance not only for the quality of life of elderly people but also because disability is closely associated with use of health and social services.2 The rising costs of the fourth age have precipitated policy discussion across the developed world,3 a national plan in Japan,4 reform of long term care funding in Germany,5 and the appointment of a Royal Commission in the United Kingdom.
The pattern of disability in the elderly population in England and
Wales was last studied in detail in 1986.6 This study showed rising rates of disability with age and significantly higher rates for women. The patterns of disability associated with cognitive impairment, however, have been less clear. 7
8 Accurate national estimates of the numbers of
cognitively impaired and physically disabled elderly people, subdivided
by a range of sociodemographic, dependency, care receipt and survival
variables are needed to support debates over the form and funding of
government health and welfare support and for local service planning.
The Medical Research Council's cognitive function and ageing study and
resource implications substudy provide a basis for contemporary
estimates. This longitudinal cohort study of elderly people began in
1991-2, and follow up data from the first 2 years provide estimates of the use of the range of provisions to those who are disabled.
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Subjects and methods |
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Study design
A full description of the study design can be found
elsewhere.9 Briefly, random population samples of people
in their 65th year and above were obtained from Family Health Service
Authority lists in six areas of England and Wales (although data on
resource use were collected in only the four sites included in this
analysis). Sites were chosen as representing the main national
variation in urban-rural differences, regional heterogeneity, and the
presence of academic groups experienced in population studies. Ethical
approval was obtained in each study site.
Scales and classification
The modified Townsend activities of daily living scale covers
washing all over, cutting toenails, getting on a bus, going up and down
stairs, doing heavy housework, going shopping and carrying heavy bags,
preparing and cooking hot meals, reaching an overhead shelf, and tying
a good knot in a piece of string. 11 12
Scores are: 0, if the person can perform the activity with no
difficulty; 1, if the person can perform the activity but with
difficulty; and 2, if the person needs help to perform the activity.
Totalled scores ranged from 0 (no incapacity), to 1 or 2 (slight
incapacity), 3-6 (some incapacity), 7-10 (appreciable incapacity), 11 or more (severe incapacity). Severe incapacity might describe a person
who needs help to do at least two of the activities and has some
difficulty with all of the rest.
3: a majority of these people have dementia.
People were classified as physically disabled if they scored
11
on the Townsend scale.11 Those with both characteristics
are referred to as having combined disability.
The interval of need for care is a classification based on the lapsed
time between periods when the subject may need help with essential
activities. 11 14 The categories for
classification are independent, long interval (needing care less often
than daily), short interval (needing care at some time every day), and
critical interval (needing care or supervision continuously). People
were allocated to the interval categories on the basis of daily living functioning (from the Townsend scale) and their score in the
mini-mental state examination.15 For example, a typical
person categorised as critical interval would be bedbound or
chairbound, or unable to get to or use the toilet, or have severe
cognitive impairment. Anyone with severe cognitive impairment
(mini-mental state score <10) was considered to need critical interval
care regardless of their physical dependency.
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Results |
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Table 1 shows the estimated numbers of disabled elderly people by type of disability, age, and sex. Using the study definitions, there were an estimated 1.3 million disabled elderly people in England and Wales (15.7% of those aged 65 and over, 95% confidence interval, 15.1% to 16.3%). These and subsequent estimates were weighted by sex and 5 year age groups to reflect the population structure of England and Wales in 1996,16 and calculation of confidence intervals took account of each age and sex weighted group separately. Prevalence rates were lower in men (10.6%, 9.7% to 11.5%) than in women (19.2%, 18.3% to 20.1%).
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Women accounted for 72% of the disabled group, with the preponderance of women becoming more pronounced with age. Cognitive impairment was present in over a third of all disabled elderly people (38.3%, 36.0% to 40.6%), and these were more or less equally divided between the cognitive only or combined categories. People aged 85 and over made up 37.6% (35.6% to 39.7%) of the total number with disability.
A good summary of overall level of dependence was the critical interval of need for care. Of the 1.3 million disabled elderly people, 3% (35 576) were independent, 14% (171 586) needed care less often than daily, 62% (778 401) needed care at some time every day (short interval) and 21% (268 863) needed care or supervision continuously (critical interval).
Only 1% of the subjects who were not disabled by study definitions
lived in institutional care. However, 17% of those with only cognitive
impairment, 18% of those with only physical disability, and 52.8%
(47.3% to 58.3%) of those with combined disability lived in
institutions. Overall, 46% of all those living in institutions had
diagnostic levels of cognitive impairment. By contrast, accommodation with a warden provided care for only 9% of those with combined disability and catered for many people who were not classified as
disabled. The proportions of disabled elderly people living alone or in
institutions increased sharply with age, especially among
women
56% of institutional places for the disabled were filled
by people aged 85 or over and 79% were filled by women.
Table 2 shows the proportions of each disability group in the community by type of help received and type of helper. Although most of the care required involved household tasks, 38% of those with combined disability received help with personal care tasks. Most of this help was supplied by informal care givers, but the contribution of formal community support including, for example, home help, care workers, meals on wheels, and community nurses, was far from insignificant. Formal services were the sole reported source of support for 29% of people who were physically disabled only and 23% of those with combined disability, and these services complemented informal support in a further 10% and 11% respectively.
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Over the 2 year period of follow up from baseline interview (undertaken in subjects in the resource implications study only, which excludes those without disability), 63.2% (60.7% to 65.8%) used acute hospitals, with 43% doing so as inpatients. Rates of acute hospital use were even higher in disabled people living in the community (table 3). Cognitive impairment was associated with relatively lower use of all forms of hospital care. For those living in the community there was also a small decrease in use of all hospital services with age, with 72% of those aged 65 to 74 using hospital care compared with 71% aged 75 to 84 and 63% of those aged 85 and over.
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In the 2 years after initial interview, 10% of the whole group of
elderly people died, but rates were far higher in those with cognitive
impairment (25%), physical disability (26%), or combined disability
(48%).
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Discussion |
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Throughout the developed world, the funding of care for disabled elderly people has become a highly publicised political issue. In the United Kingdom, total public expenditure on long term care is already estimated to account for 3.6% of the gross domestic product,17 and some have suggested that overall costs might rise as high as 10.8% by 2030.18 Not surprisingly, UK governments have undertaken a series of reforms in this area, including narrowing access to NHS continuing care and thereby extending means testing.19 In future policy debates, estimates of the numbers and types of people who need long term care should be central.
Comparison with general household survey estimates
Several problems with the estimates presented above should be
noted. The four areas included in the study are diverse, but are not
fully representative of England and Wales. However, comparisons of
study estimates for 1991 with those produced by the nationally
representative general household survey for the same
year20 mostly show remarkable similarity, for example, in
the proportion of people living at home who had no difficulty with
particular tasks. However, reported proportions of elderly people who
were living in residential or nursing home care in 1994 were marginally
higher than study estimates for that year.21 These
differences may be the result of having no study sites in
the retirement areas of the country. However, government policy aims to
reduce rates of elderly people living in nursing and residential
homes and thus the estimates presented give a picture that is
appropriate for future care planning.
Implications
In considering the results, it is important to remember that
disability is not an attribute that is clearly present or absent, but
rather a matter of degree. While policy makers may like to classify
people as fit or disabled, in need or not, in reality a full spectrum
of disability is present, from slight to very severe. This lack of a
natural cut off point between those in need of long term care and
those not in need of long term care has obvious implications for
establishing workable eligibility criteria for long term care funding.
It also means that providers of care have substantial scope to offer
services to comparatively less disabled groups, thus expanding the size
and cost of long term care programmes.
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Acknowledgments |
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We thank the subjects, the project team of the resource implications study, and the fieldworkers.
Contributors: Study Management Group: T Arie, J Bond, C Brayne, JRM Copeland, NE Day, M Devakumar, ME Dewey, M Esiri, O Goddard, B Gregson, J Grimley Evans, FA Huppert, M Jepson, AL Johnson, DWK Kay, C McCracken, I McKeith, K Morgan, J Morris, C Parker, ES Paykel, and N Walker. National coordinators: C McCracken and GP Slegg. Cambridge: C Brayne, FA Huppert, J Nickson, and ES Paykel. Gwynedd: JRM Copeland, M Devakumar, ME Dewey, and S Jones-Evans. Liverpool: JRM Copeland, ME Dewey, P McKibbin, and P Saunders. Newcastle: A Fairbairn, S Hrisos, J Illing, DWK Kay, and I McKeith. Nottingham: T Arie, J Levings, K Morgan, and C Parker. Oxford: J Grimley Evans and O Goddard. Medical Research Council Biostatistics Unit: C Gill, AL Johnson, D Mathewson, MA McGee, J Nickson, and N Walker. Analysis subcommittee: C Brayne, JRM Copeland, NE Day, ME Dewey, C Gill, B Gregson, FA Huppert, J Illing, AL Johnson, DWK Kay, D Mathewson, C McCracken, MA McGee, K Morgan, J Nickson, C Parker, ES Paykel, and N Walker. Instrument subcommittee: J Bond, C Brayne, JRM Copeland, NE Day, ME Dewey, C Gill, B Gregson, J Grimley Evans, FA Huppert, AL Johnson, DWK Kay, C McCracken, I McKeith, K Morgan, P Saunders, and N Walker. Local administrators and support staff: B Ackerly, V Gilgeous, L Hughes, V Jackson, J Pollock, and A Scott.
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Footnotes |
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1 Writing committee: David Melzer, Brenda McWilliams, Carol Brayne, Tony Johnson, John Bond Department of Community Medicine, University of Cambridge, Institute of Public Health, Cambridge CB2 2SR David Melzer, clinical senior research associate Brenda McWilliams, research associate Carol Brayne, lecturer in epidemiology Medical Research Council Biostatistics Unit, University of Cambridge, Institute of Public Health Tony Johnson, medical statistician Centre for Health Services Research, University of Newcastle upon Tyne NE2 4AA John Bond, professor of health services research
Funding: The Medical Research cognitive function and ageing study was funded by the Medical Research Council and Department of Health. The analyses reported were funded by a grant from the Anglia and Oxford research and development programme.
Competing interests: None declared.
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References |
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rights and responsibilities.
London: Stationery Office
, 1999(Cmnd 4192-1.)
(Accepted 18 February 1999)
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