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BMJ 2004;328:1102 (8 May), doi:10.1136/bmj.328.7448.1102
Anita Patel, lecturer in health economics1, Martin Knapp, professor of health economics1, Andrew Evans, clinical lecturer in stroke medicine2, Inigo Perez, research fellow2, Lalit Kalra, professor of stroke medicine2
1 Centre for the Economics of Mental Health, Institute of Psychiatry, London SE5 8AF, 2 Department of Medicine, Guy's, King's and St Thomas's School of Medicine, London SE5 9PJ
Correspondence to: L Kalra lalit.kalra{at}kcl.ac.uk
Objective To evaluate the cost effectiveness of caregiver training by examining health and social care costs, informal care costs, and quality adjusted life years in care givers.
Design A single, blind, randomised controlled trial.
Setting Stroke rehabilitation unit.
Subjects 300 stroke patients and their care givers.
Interventions Caregiver training in basic nursing and facilitation of personal care techniques compared with no caregiver training.
Main outcome measures Health and social care costs, informal care costs, and quality adjusted life years in care givers over one year after stroke.
Results Total health and social care costs over one year for patients whose care givers received training were significantly lower (mean difference -£4043 ($7249;
6072), 95% confidence interval -£6544 to -£1595). Inclusion of informal care costs, which were similar between the two groups, did not alter this conclusion. The cost difference was largely due to differences in length of hospital stay. The EQ-5D did not detect changes in quality adjusted life years in care givers.
Conclusion Compared with no training, caregiver training during rehabilitation of patients reduced costs of care while improving overall quality of life in care givers at one year.
Assessment of caregiver quality of life
We used the EuroQol five-dimensional questionnaire (EQ-5D)10 at baseline, and at 4, 12, 26, and 52 weeks after stroke to carry out assessments. We imputed missing values for care givers with partially missing EQ-5D data by carrying forward the last value. We applied utility weights from a UK general population survey to EQ-5D health states to calculate quality adjusted life years (QALYs). We examined QALY outcomes in terms of change between baseline and week 52 (see bmj.com)
Use of resources
We adopted a societal perspective, including health services, other formal care agencies, and informal carers for the economic evaluation. We collected data on use of health and social care services over one year after onset of stroke and on use of hospital resources for a three month period before stroke. Therapists recorded data on hospital use and therapy input after stroke. We used a specially adapted version of the client service receipt inventory to collect data on use of services after discharge from hospital retrospectively, at 12, 26, and 52 weeks during patients' assessment interviews.11
Costs
To obtain a cost per patient we multiplied resource volumes by unit costs. We used the opportunity cost method to estimate the cost of informal care. We used the United Kingdom minimum wage (then £4.10 per hour) as a proxy valuation of care givers' time. We standardised all costs to 2001-2 prices. See bmj.com for details.
Data analysis and statistical methods
The primary outcome measure for the study was health and social care costs during the first year after onset of stroke. We analysed the data on an intention to treat basis. Data were incomplete for those patients who died before the end of the study and their care givers, and for some survivors and their care givers. We included all available data in the analyses. We used Student's t test to compare differences between groups and non-parametric bootstrap methods, with 5000 repetitions, to obtain 95% confidence intervals.
Quality adjusted life years
Mean QALY values for trained and untrained care givers were comparable at baseline (0.94 (SD 0.10) v 0.94 (SD 0.14)) and at one year (0.91 (SD 0.11) v 0.90 (SD 0.14)). We found no significant difference between groups in QALY losses between baseline and one year. Given that the visual analogue scale detected changes over time and a difference between the groups,9 it is likely that the EQ-5D was insensitive to change in caregiver health related quality of life, rather than that there were no effects on QALYs.
Resource use and costs
The two groups used resources to a similar extent at baseline. Patients in the training group stayed in hospital less long (mean difference -12.4 days, 95% confidence interval -19.5 to -5.6) and had less physiotherapy (-30.2 units, -51.8 to -8.9) and occupational therapy (-3.2 units, -4.8 to -1.6) than patients in the no training group. Use of speech and language therapy was similar between the two groups. About a third of patients in both groups received help from social services with personal care, and 14-17% received domestic help. Although a trend towards lesser use of personal and domestic care services became obvious in the training group, the difference was significant only for use of day care (-2.8 visits, -5.1 to -0.5).
Sixty per cent of total annual costs in each group were accounted for by bed days during the initial admission, which rose to 80% after including therapy costs (table 1). These costs were significantly lower in the training group and were due to the shorter initial stay in hospital rather than reduced costs in the 12 months after stroke.
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The number of care givers providing assistance to patients in various informal care activities increased in both groups compared with baseline. We found no significant differences in the average number of care hours provided per day, the number of days that such care was provided, or the total average annual number of care hours. Informal care, costed at minimum wage, amounted to an average of £884 ($1585;
1328) (SD £1482) in the training and £933 (SD £1283) in the no training group. The addition of these to total annual costs did not alter the finding that the training group had lower total costs.
Sensitivity analyses
We carried out sensitivity analyses on two aspects of the evaluation to assess the robustness of the findings. First, we used the replacement cost method to estimate the costs of informal care. This did not affect comparisons of total costs. Secondly we examined the effect of increasing the length of stay of patients in the training group by 10%, 15%, and 20%. Differences between the groups in hospitalisation costs remained, with an up to 15% increase in the training group's length of stay and in total annual costs for health and social care with up an to 20% increase in length of stay (see bmj.com)
Training care givers did not substantially reduce use or costs of resources in the community after discharge from hospital. The possibility exists that the trends towards lower personal and domestic care costs may have reached significance in a larger sample.
Potential biases
Cost advantages seem to be a result of earlier discharge from hospital in the training group. This unexpected finding has several potential explanations. The most likely reason is that training and some input into care before discharge may have increased the confidence and competence of care givers. It is also possible that patients' and care givers' awareness that they were receiving extra interventions or these families being viewed as "special" by the multidisciplinary team may have expedited discharge, although there was no evidence that they received more therapy input, or more community support after discharge. Finally, the possibility of bias due to unblinding was considered to be small because length of hospital stay was not a predefined outcome measure, the team deciding discharge was different to the research team, and sensitivity analyses showed that findings remained valid even when the length of stay was increased by 20% in these patients.
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Weaknesses of the study
Assessment of costs did not include the initial investment into developing the training intervention. The ongoing costs of training care givers were also embedded within the activity returned by the therapists and difficult to dissect from overall costs of therapy. The costs suggested by the protocol are likely to be an underestimate that does not reflect true service costs. The inclusion of these costs would equalise costs of therapy but not affect comparisons between groups.
The EQ-5D seemed insensitive to changes in care givers' QALYs. Although it has been used successfully with care givers,12 others have shown it to be less sensitive.13 14
Strength of the study
We examined costs as well as changes in health outcomes. In addition, the study takes into consideration the possibility of shifting costs from statutory services to informal care and shows that caregiver training can reduce costs of formal care without shifting costs on to care givers, while improving clinical outcomes in care givers and patients.9
Conclusion
Despite care givers being recognised as one of the building blocks of community care, little is known about how care givers can be assisted effectively. Improving the skills of consenting informal care givers during inpatient rehabilitation reduces stroke care costs and improves their quality of life without increasing the burden of care to families or transferring costs to the community.
The health economics checklist is on bmj.com
This is the short version of the paper; the long version is on bmj.com
We acknowledge the contributions made by all hospital, general practice, community health, and social services staff to the project. Particular thanks are owed to Shirley Law and Caroline Oates of the Carer Information and Support Services in Bromley and to Jayne Steadman, Judith Eade, and Magreet Whittink, who participated in the caregiver training programme.
Funding: NHS R&D Executive's Primary Secondary Interface Priority Programme (Project No: F-4/1997).
Competing interests: None declared.
Ethical approval: Bromley Research Ethics Committee (LREC/106).
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