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Division of Health in the Community, Medical School Building, University of Warwick, Coventry CV4 7AL, e-mail: B.Sheehan{at}warwick.ac.uk
Coventry Teaching PCT, Caludon Centre, Coventry
B.S. has received support to attend a conference from Janssen-Cilag and Eisai. K.S. has received sponsorship from Shire, Janssen-Cilag, Eisai, Pfizer, Lundbeck and Novartis.
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Abstract |
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To describe a targeted domiciliary drug treatment service for dementia and to establish clinical outcomes for its patients. All new referrals in a 6-month period were included. Data on clinical and demographic background, service performance and cognitive, functional and behavioural outcomes were recorded.
RESULTS
Of 96 patients initiated on antidementia drugs, most had dementia of mild to moderate severity, and had heterogenous diagnoses. Significant improvements in cognition, behaviour and function were found.
CLINICAL IMPLICATIONS
A dedicated domiciliary drug treatment service for dementia achieved high levels of clinical activity and outcomes at least as good as clinical trials. This service model may be an attractive choice.
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Introduction |
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The aims of this paper are: (a) to describe this service; (b) to establish activity/case mix; (c) to assess clinical outcomes for patients of this service.
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Method |
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Demographic/clinical data
We recorded age, gender, living and care arrangements and the diagnosis
given in the consultant referral letter.
Service data
We recorded time from referral to assessment and from initiation of
treatment to first reassessment. We also recorded the drug used and the
outcome of the assessment (continuation/or stopping drug).
Outcome data
Cognition was measured using the Mini-Mental State Examination (MMSE;
Folstein et al, 1975)
or Addenbrookes Cognitive Examination (ACE;
Mathuranath et al,
2000). Function was measured with the Bristol-Activity of Daily
Living scale (B-ADL; Bucks et al,
1996). Behaviour was recorded using Behave-AD
(Reisberg et al,
1987).
Summative and descriptive statistics were used to describe the patient group. To analyse change in assessment scores over time, paired t-tests (for normally distributed scores) or Wilcoxon matched-pairs signed-ranks tests (for non-normally distributed scores) were used.
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Results |
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Of the 96, 55 (57.3%) were given a diagnosis of Alzheimers disease, 18 (18.8%) vascular dementia, 3 (3.3%) mixed vascular/Alzheimer dementia, 13 (13.5%) were recorded as dementia unspecified, and 7 had other diagnoses recorded, including dementia with Lewy bodies, dementia in multiple sclerosis and mild cognitive impairment. Mean age was 80.1 years (range 59-98) and 64 (66.7%) were female. Thirty-five (36.5%) lived alone. Mean baseline MMSE score was 20.0 (range 0-28). Seventy-five (78.1%) were initiated on donepezil, 9 (9.4%) on galantamine, 5 (5.2%) on rivastigmine and 7 (7.3%) on memantine. Mean time from referral to baseline assessment was 7.3 weeks (range 0-29). Of those initiated, 19 (19.8%) withdrew before the 3-month assessment could be completed. Eleven withdrew owing to side-effects, 4 owing to physical illness developing, 3 were nonadherent with medication and 1 died before reassessment. First reassessments were completed (n=77) a mean of 3.7 months after initiation of the drug. Of the 77 patients completing the course of treatment, 69 (89.6%) were judged responders and continued on treatment. Table 1 shows the outcomes according to assessment scores for those completing.
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There was a statistically highly significant improvement in scores measuring cognition, behaviour and function.
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Discussion |
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The service conforms to current NICE guidance, which recommends specialist diagnosis and initiation of treatment, assessments of cognition, activities of daily living, and behaviour, and assessment of response 2-4 months after initiation of treatment. The service treats large numbers of patients and our outcomes are comparable to, or better than, those found in both published randomised controlled trials of antidementia drugs (Rogers et al, 1998; Reisberg et al, 2003) and in reports of open studies of the use of donepezil in a UK memory clinic (Mathews et al, 2000). In particular, we believe the demonstration of benefits for cognition, function and behaviour is important. Our drop-out rate is comparable to those in controlled trials (Rogers et al, 1998; Wilcock et al, 2000).
This study has a number of limitations. Significant benefits may follow from non-specific aspects of the service, such as instillation of hope and initiation of nondrug services suggested by the teams nurses. It was beyond the scope of this study to consider the economic implications of introducing this service configuration and there was no comparison arm of another such service. Importantly, patients referred to the service were heterogenous in terms of both diagnosis and severity of illness and a variety of drug treatments were initiated. We believe that the offer of treatment to some patients with diagnoses other than Alzheimers disease, and the use of a range of available drugs, is probably typical of practice in the UK, which may make our outcomes more generalisable.
The clinical implications of this study are that a dedicated home-based service for the drug treatment of dementia can achieve high levels of clinical activity, is adherent to NICE recommendations on assessment protocols and achieves comprehensive outcomes at least as good as those reported in controlled trials. The recent report on the AD2000 trial (AD2000 Collaborative Group, 2004) and recent uncertainty in the UK over future availability of antidementia drugs have drawn attention to the possibility that clinical benefits from the use of cholinesterase inhibitors may be too small to justify their cost. Although this is an open report of service outcomes, with resultant biases, we believe that the outcomes reported show a real clinical benefit for patients/carers. We believe that models of service delivery may have substantial impacts on patient outcomes and that this model may be attractive to services deciding how best to organise treatment for this vulnerable group.
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Acknowledgments |
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References |
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This article has been cited by other articles:
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A. J Pelosi, S. V McNulty, and G. A Jackson Role of cholinesterase inhibitors in dementia care needs rethinking. BMJ, September 2, 2006; 333(7566): 491 - 493. [Full Text] [PDF] |
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