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Objectives To assess the long term clinical and cost effectiveness of the diabetes education and self management for ongoing and newly diagnosed (DESMOND) intervention compared with usual care in people with newly diagnosed type 2 diabetes.
Setting Primary care trusts in the United Kingdom.
Participants Patients with newly diagnosed type 2 diabetes.
Intervention A six hour structured group education programme delivered in the community by two professional healthcare educators.
Main outcome measures Incremental costs and quality adjusted life years (QALYs) gained.
Results On the basis of the data in the trial, the estimated mean incremental lifetime cost per person receiving the DESMOND intervention is £209 (95% confidence interval −£704 to £1137; €251, −€844 to €1363; $326, −$1098 to $1773), the incremental gain in QALYs per person is 0.0392 (−0.0813 to 0.1786), and the mean incremental cost per QALY is £5387. Using “real world” intervention costs, the lifetime incremental cost of the DESMOND intervention is £82 (−£831 to £1010) and the mean incremental cost per QALY gained is £2092. A probabilistic sensitivity analysis indicated that the likelihood that the DESMOND programme is cost effective at a threshold of £20000 per QALY is 66% using trial based intervention costs and 70% using “real world” costs. Results from a one way sensitivity analysis suggest that the DESMOND intervention is cost effective even under more modest assumptions that include the effects of the intervention being lost after one year.
Conclusion Our results suggest that the DESMOND intervention is likely to be cost effective compared with usual care, especially with respect to the real world cost of the intervention to primary care trusts, with reductions in weight and smoking being the main benefits delivered.
Type 2 diabetes mellitus affects around 5% of people in European populations and is responsible for a disproportionate use of health service resources.1 In the short term, diabetes can be accompanied by various symptoms such as fatigue, and in the long term it can lead to serious complications such as blindness, renal failure, and amputation.2 Furthermore, diabetes is associated with increased morbidity and premature death from cardiovascular diseases, including stroke and myocardial infarction. Lifestyle advice on diet and exercise is at the core of first line management of diabetes, either alone or with concomitant use of drugs such as metformin.3 However, patients find it difficult to implement and sustain lifestyle advice given by healthcare professionals.4
The national service framework for diabetes and the 2008 National Institute for Health and Clinical Excellence diabetes guideline5 explicitly state that all primary care trusts should offer structured education programmes to people with type 2 diabetes from the point of diagnosis. The diabetes education and self management for ongoing and newly diagnosed (DESMOND) intervention for people with newly diagnosed type 2 diabetes was one of the first programmes to meet the criteria for suitable education programmes laid down by the National Institute for Health and Clinical Excellence and is currently available in at least 80 primary care trusts in England and Scotland. The programme, which is facilitated by registered healthcare professionals trained as educators, comprises six hours of contact time during a full day or as two half day sessions. The curriculum focuses on lifestyle factors, such as food choices and physical activity, and cardiovascular risk factors.
Before the trial of the DESMOND programme, which started in 2004,6 there was no evidence that structured education from the point of diagnosis provides added benefit for patients beyond usual care. The cluster randomised trial took place in 13 primary care sites (162 practices) involving 1109 patients with type 2 diabetes who were referred within four weeks of diagnosis. A total of 824 (74%) individuals consented and were assigned to either the DESMOND intervention or standard care on the basis of which study arm their practice was randomised to. Those randomised to the intervention completed the structured group education programme within 12 weeks. The study design, baseline characteristics of the patients, and changes in biomedical, lifestyle, and psychosocial measures over 12 months in the 91% of participants with follow-up data at 12 months have been reported previously.6 7 8 Analyses of the trial data showed improvements in weight, smoking cessation, illness beliefs, and depression scores in patients who received the intervention compared with those on standard care.6
To date, there has been no economic evaluation of the DESMOND intervention, or any similar education intervention in the United Kingdom, to assess whether the benefits reported in our trial represent a cost effective return on the intervention compared with either no education or ad hoc and unevaluated education (that is, usual care). This study examines the cost and utility of the DESMOND programme when assessed against the National Institute for Health and Clinical Excellence’s cost effectiveness acceptability threshold of £20000 (€23982; $31191) per quality adjusted life year (QALY),9 based on intervention costs both from the earlier trial and as currently being implemented in a UK primary care setting.
The costs of delivering the DESMOND programme and its effects on health related quality of life, particularly in relation to reductions in weight and smoking, will accrue over the long term, and, therefore, an analysis using only the 12 month outcomes from our previous trial would be inappropriate. We incorporated the 12 month trial results into a long term model of diabetes—the Sheffield type 2 diabetes model—that accounts for the long term effects of the intervention on smoking and weight as well as on the biomedical measures (that is, levels of glycated haemoglobin (HbA1c), cholesterol, and systolic blood pressure) that affect comorbidities of diabetes, such as cardiovascular disease, retinopathy, neuropathy, and renal complications.
The trial based inputs we planned to use in the diabetes model needed to take account of the clustered nature of the data (that is, randomisation was at practice level).6 Consequently, these inputs were analysed using robust generalised estimating equations,10 11 with exchangeable correlation structure. For binary outcomes, a logit link with a binomial distribution for the outcome was used. For continuous outcomes, an identity link with a normal distribution was used. For ordinal outcomes, we used an ordinal regression model with proportional odds assumption, adjusted for clusters.12 As well as adjusting for clustering, additional covariates were incorporated into the statistical models as deemed appropriate for the specific analyses being undertaken. Analyses were done using STATA 10.0/SE for Windows. Missing outcomes were not replaced and analyses were carried out on an intention to treat basis.
The overall approach to the economic evaluation is in line with the reference case methods for National Institute for Health and Clinical Excellence technology appraisals. The economic evaluation component used an NHS and personal social services perspective for costs, and health outcomes measured in QALYs were based on EQ-5D values. Both costs and QALYs were discounted at 3.5% per annum in line with current National Institute for Health and Clinical Excellence guidance.9
We undertook a bottom up costing exercise to calculate the average cost per patient of delivering the DESMOND programme within the trial (table 11).). Some items of expenditure, such as the training of educators and non-consumable purchases for the course (for example, food models, display boards), provided resources for use over a much longer period than the trial. Research costs, including one additional general practitioner visit, were excluded from the costs of the programme. Non-recurrent costs were spread over a three year period using annuitisation at a rate of 3.5% a year, with the equivalent annual cost being included in the calculation of the cost of the course.
The costs of delivering the programme in primary care have changed since the trial because the DESMOND team has a better appreciation of resource requirements and was able to capture the economies of scale through widespread delivery of the programme (for example, more participants per educator). Therefore, we also estimated the “real world” cost of the components of the programme for a hypothetical primary care trust with an average population of 329550 patients. We also assumed a total of 56 DESMOND courses would be run each year by three educators and an average of 10 patients per course.
Trial data were used to identify use of drugs and use of general practitioners’ and other primary care professionals’ time over 12 months. Medication use was recorded at four month intervals in the trial, so we estimated an individual’s aggregated drug use over the 12 months of the trial from the usage recorded at baseline, month four, month eight, and month 12. Unit costs of drugs were obtained from the NHS Information Centre for Health and Social Care’s prescription cost analysis 200713 and a weighted average of the most frequently used drugs in each class was used. Unit costs for visits to a general practitioner and other consultations were obtained from the Personal Social Services Research Unit’s unit costs of health and social care 2007.14
Differences between the control and the intervention group in drug use and use of NHS resources are shown in table 22.. These costs were then combined and reanalysed to adjust for clustering and covariates that were relevant to both drug and resource.
Unit costs relating to long term complications were obtained from a variety of published sources, the most significant ones for this evaluation being costs of events relating to cardiovascular disease and comorbidities, which were obtained from United Kingdom Prospective Diabetes Study number 65 (UKPDS 65).15 These data were adjusted to 2008 levels using the Hospital and Community Health Services Pay and Price Index.14
In the long term model described later, the differences between biomedical measures at baseline and these characteristics at 12 months in the trial of the DESMOND intervention were incorporated into the characteristics of patients at baseline, as shown in table 33.. Lifestyle changes might not be sustained without an ongoing maintenance intervention, so we assumed that the effects observed would be completely lost three years after the end of the intervention.
Smoking status at entry to the long term model was based on the conditional probabilities shown in table 44,, which relate final smoking status in the trial of the DESMOND intervention to that at baseline. This shows that, compared to patients in the control arm, there was a greater probability of patients in the intervention arm stopping smoking, and less chance of non-smokers starting smoking. We obtained annual relapse rates from an analysis16 of British Household Panel Survey data and used these to model the probability that a patient who had quit smoking during the trial subsequently relapses. We calculated a relapse rate of 19.6% after one year of abstinence, which decreases to 3.8% at five years and 1.6% at 12 years.
After adjustment for age, gender, HbA1c, smoking status, use of drugs known to affect weight (for example, oral hypoglycaemic agents, diuretics), baseline values, and clustering, there was a −1.26 kg (95% CI −2.19 to −0.34) difference in weight between the intervention arm and the control arm at 12 months. This effect may not be sustained without an ongoing maintenance intervention, so we assumed that it was completely lost three years after the end of the intervention.
The odds ratio for using an oral hypoglycaemic agent at month 12 was 0.79. This was used to apply differential rates of oral hypoglycaemic agent use to the two treatment arms in the long term model. We assumed that the first line oral hypoglycaemic agent is metformin, after which a sulphonylurea is added, followed by switching to insulin plus metformin. Given that there was negligible difference between study arms in the rate of statin use at month 12 of the trial (odds ratio=0.99), we applied the same rate (75%) at baseline to the two arms in the long term model. There was a higher rate of antihypertensive therapy use at month 12 in the intervention arm, but this difference was not statistically significant (odds ratio 1.18, 95% CI 0.71 to 1.98). This equates to only 4% higher usage in the intervention arm, equivalent to an additional cost of about £2, so we assumed equal rates of antihypertensive use in the long term model.
Health related quality of life data were recorded from trial participants using the EQ-5D questionnaire at baseline and at four, eight, and 12 months. The EQ-5D questionnaire uses five dimensions of health (mobility; self care; usual activities; pain and discomfort; and anxiety and depression), each of which is assessed by a single question and scored on a three point ordinal scale (no problems; some problems; or extreme problems). We combined the five dimension scores at each time period into a single preference score using the standard UK algorithm.17 The incremental gain in QALYs during the trial in patients who received the DESMOND intervention was 0.0070 (95% CI −0.0126 to 0.0491)
The decrements in health related quality of life attributable to diabetes and complications of diabetes that we used in the long term model were based on UKPDS data where possible,18 with values for additional comorbidities obtained from Coffey et al.19 Utility changes associated with weight gain were based on a simple weighted average of two studies20 21—a 0.0025 (95% CI 0.0003 to 0.0048) utility decrement per kg increase in weight. A recent review of weight and health related quality of life in patients with or without type 2 diabetes reported similar results.22
The Sheffield type 2 diabetes model is an integrated individual level simulation model23 that estimates—using changes in key risk factors such as smoking status, HbA1c level, lipid concentration, and blood pressure—the effect of alternative interventions on long term incidence of diabetic complications and mortality, and the associated economic effects of such interventions and outcomes. The model also includes side effects such as hypoglycaemic attacks and, importantly for this assessment, the ability to estimate the effect of weight changes on health related quality of life. A description of the Sheffield type 2 diabetes model and a model structure diagram appear in web extra 1 and web figure A, respectively.
The main outcome in our long term modelling was the incremental cost per QALY gained in patients who received the DESMOND intervention compared with those who received usual care. The time limit used for the long term modelling was 80 years (effectively lifetime for this age group).
The UKPDS coronary heart disease and stroke risk engines use smoking status at diagnosis of diabetes as a risk factor.24 25 We assumed that current smoking status can be applied in these equations so that ongoing risk estimates of cardiovascular disease take account of changes in smoking status. Comparison of the hazard ratios from these risk engines with those from the UKPDS outcomes model26 (which uses current smoking status) suggests that this is a reasonable assumption. The effect of smoking on other cause mortality was based on the hazard ratio reported in the UKPDS outcomes model.
The mean characteristics of patients at entry to the long term model are shown in table 55 and reflect the mean adjusted differences between the intervention and the control (that is, adjustment was made to eliminate differences at baseline between the two study arms of the trial). Prevalence of atrial fibrillation was not obtained from the DESMOND data but assumed to be 1% on the basis of UKPDS data.
The approach to the handling of uncertainty was essentially Bayesian, with values being sampled from distributions for parameters (for example, HbA1c level, weight) to capture uncertainty around the mean estimates. A probabilistic sensitivity analysis was conducted by combining 500 random samples from the trial results, obtained using bootstrapping, with 500 sample results from probabilistic sensitivity analysis each with a cohort size of 100 patients.27 This approach assumes that the incremental costs during the trial were independent of incremental costs from the long term model; likewise for incremental QALYs gained. This assumption was considered reasonable because economic outcomes arising during the trial are strongly driven by the effect of undertaking lifestyle changes during the trial, whereas economic outcomes from the long term model are more complex, with results being more driven by uncertainty in model parameters, such as the coefficients used in the cardiovascular risk equations. Probabilistic sensitivity analyses were undertaken using both trial and real world costs of delivering the DESMOND programme.
We also undertook a sensitivity analysis using more conservative assumptions, in particular concerning the durability of the effects of the DESMOND intervention observed at the end of the trial. Changes in biomarkers (including weight) were assumed to last for only one year from the end of the trial, smoking relapse rates were scaled up by 25%, and a lower hazard ratio was assumed for other cause mortality due to smoking (1.24 v 1.36 for the base case analysis).
On the basis of our costing exercise, the estimated cost of delivering the DESMOND programme in the 12 month trial of the intervention was £203 per patient. The equivalent real world cost per patient for a hypothetical primary care trust was estimated to be £76. Costs would vary, however, depending on local circumstances (for example, population size, pay scales of staff, number of staff trained). The cost of the DESMOND programme in terms of its effect on drug use and use of NHS resources was £16 in the trial, which differs from the sum of the two individual components shown in table 22 because of adjustment for clustering and covariates that were relevant to both drug and resource. Adding this value to the £203 cost of the intervention during the trial gives an estimated 12 month total incremental cost for the DESMOND intervention arm of £219. Using the £76 real world cost of the intervention, the total incremental cost was £92.
The results from the economic modelling are shown in table 66.. Modelled lifetime costs—which incorporate drug costs, monitoring, and costs of complications from the end of month 12 to 80 years—are almost identical at £15836 in the control arm and £15826 in the intervention arm, a difference of just £10 (discounted). Therefore, the total lifetime cost of patients receiving the DESMOND intervention is £16289 using trial based intervention costs and £16162 using real world costs, £209 (95% confidence interval −£704 to £1137) and £82 (−£831 to £1010) more expensive than usual care, respectively.
The mean cluster adjusted gain in QALY with the DESMOND programme up to month 12 in the trial is estimated at 0.0070, equivalent to an average gain of 2.55 days of perfect health per person over the year. The long term gain in QALYs (end of month 12 to remaining lifetime) is estimated at 0.0322, so the total estimated gain in QALYs for patients who received the DESMOND intervention compared with those who received usual care was 0.0392—equivalent to a discounted average gain of 14.2 days of perfect health per person over their lifetime. The estimated incremental cost per QALY gained is £5387 using trial based intervention costs and £2092 using real world costs. Such estimates are well within the threshold of £20000 to £30000 per QALY usually considered by the National Institute for Health and Clinical Excellence and other bodies as cost effective.
The cost effectiveness acceptability curves (fig 11)) show that the probability of the DESMOND programme being more cost effective than usual care is fairly similar whether trial or real world intervention costs are used. Using trial costs, the probability of the DESMOND programme being more cost effective than usual care is 0.66 for an acceptability threshold of £20000 per QALY (0.68 for a threshold £30000 per QALY). Using real world costs, the probability is 0.70 for both an acceptability threshold of £20000 and a threshold of £30000 per QALY. The probability of the DESMOND programme being cost saving in the long term is 0.28 using trial costs and 0.40 using real world costs. The probability of the DESMOND programme resulting in long term gains in QALYs is 0.70 and 0.71 using trial and real world costs, respectively.
The probabilistic sensitivity analysis results presented in figure 22 show the spread of the real world cost effectiveness estimates on a plane. Although neither the mean incremental cost nor the mean incremental QALYs reach an arbitrary 5% significance level, the probability of an intervention being cost effective is determined from a joint assessment of incremental costs and incremental QALYs. On the plane, 70% of the sampled data lie within the cost effective region to the right of the cost effectiveness “frontier,” indicating a probability of the DESMOND intervention being cost effective of 0.7.
The sensitivity analysis, which adopted a more conservative assumption relating to the durability of the effects observed at the end of the trial and a lesser effect of smoking on other cause mortality, did not change the results substantially. The incremental cost per QALY using the real world intervention costs was actually marginally lower than in the original analysis, at £1618 compared with £2092, with a 0.71 probability of cost effectiveness.
Taking account of simulated longer term effects, there is a 66% likelihood that the DESMOND intervention as delivered during the trial of the intervention is cost effective. Furthermore, the intervention is even cheaper as currently implemented in the real world, costing £76 per patient compared with £203 each in the trial. This disparity is a result of economies of scale and some unavoidable high costs during the trial (for example, residential courses were required to train educators attending from across the country). As such, the likelihood that the DESMOND programme is cost effective in the real world is, at 70%, higher than in the trial. When the analysis was restricted to the costs and benefits within the 12 month time frame of the trial, the DESMOND intervention does not appear to be cost effective, as is often the case for an intervention aimed at preventing the long term effects of a chronic disease, although there is much uncertainty around the results.
Our results suggest that the DESMOND intervention is likely to be cost effective compared with usual care, especially with respect to the current cost of the intervention to primary care trusts. However, concluding that the intervention is likely to be cost effective despite the relatively small (and not all statistically significant) trial outcomes in terms of between group differences is at first sight counterintuitive. In order to make this conclusion, it is necessary to take into account both the size and the likelihood of health gains. Firstly, the nature of the intervention should be taken into account—that is, the DESMOND programme targets multiple risk factors. As such, it is the overall benefit of what are often small changes that needs to be considered. The collective mean estimated benefit of the changes arising from the DESMOND intervention is sufficient to outweigh the low intervention cost per patient. Indeed, the estimated mean health gains as measured by QALYs gained are equivalent to half a month of full health, an economically adequate return for a low cost investment. In other disease areas, treatments can cost tens of thousands of pounds per patient for the equivalent of several months QALY gains. Secondly, the likelihood of the intervention being cost effective, in this case 70%, reflects the methods of economic evaluation, which, rather than focusing on type 1 or type 2 errors, consider the costs and health gains simultaneously.
The most economically significant benefits of the DESMOND programme are reductions in overall cardiovascular risk (mainly resulting from reduced smoking rates, as shown in table 44,, but also improvements to lipids, as shown in table 33),), leading to greater survival. Together with a reduction in weight, these benefits lead to economically significant gains in QALYs (as shown in table 66).
It is interesting that the sensitivity analysis reduced the cost of the DESMOND programme per QALY gained. One might expect the more conservative set of assumptions used in the sensitivity analysis to increase rather than decrease the intervention cost per QALY gained. The main reason for this slightly counterintuitive result is that the more conservative assumptions reduce the incremental cost difference between the intervention and control arms. This is because, in the sensitivity analysis, a lower hazard ratio was assumed for other cause mortality due to smoking, resulting in extended survival in both study arms. The additional survival benefit was greater in the control patients as there were more smokers in this arm, resulting in greater exposure to the risk of complications, which require costly treatments.
Our analysis uniquely represents a detailed long term economic evaluation of a structured education programme based on results from a UK based randomised controlled trial that was carried out in accordance with a robust evaluation framework.28 Given that this was a large multi-site trial, the results are more representative than if we had used single centre studies.
The main areas of uncertainty around the results concern the effect of smoking on mortality and the durability of benefits such as improved rates of smoking and weight loss. For some risk factors used in the long term model, the differences between treatment groups were relatively small or were not statistically significant. Nevertheless, uncertainty around such effects is captured within the results of the probabilistic sensitivity analysis, and the benefits reported are economically significant when set against the low cost of the intervention. Furthermore, a sensitivity analysis that assumed the benefits only last for one year beyond the end of the 12 month trial and applied a lesser effect of smoking on mortality still showed a 71% likelihood that the intervention is cost effective.
There are few other studies against which meaningful comparisons can be made because of the heterogeneity of the interventions across studies (for example, different amounts of education provided by various health professionals; different timing of the intervention relative to diagnosis of diabetes) and lack or limitations of economic evaluations in type 2 diabetes.
A review for the National Institute for Health and Clinical Excellence on the use of patient education models29 reported an evaluation of the Dose Adjustment For Normal Eating (DAFNE) intervention for type 1 diabetes. The review concluded that the intervention is both cost saving and generates health benefits compared with conventional treatment, even under modified conservative assumptions adopted by the technology assessment group. A recent review of the clinical effectiveness of diabetes education models for type 2 diabetes30 describes two studies in the United States that were considered to be limited in their applicability and generalisability. The review did not draw any conclusions on the overall cost effectiveness of the education models. Another recent review focusing on the cost effectiveness of diabetes education31 refers to several economic studies involving differing amounts of education provided by various health professionals. The authors conclude that diabetes education is likely to be cost effective, especially when provided to patients with the poorest glycaemic control.
Two other well known diabetes education studies, the Turin study32 and the Expert Patient Education versus Routine Treatment (XPERT) programme,33 assessed patients with established type 2 diabetes. However, economic evaluations of these studies have not been undertaken. The need to offer optimal intervention from diagnosis in patients with diabetes is supported by the legacy effect observed from the long term follow-up data of the UKPDS.34
Although it is likely that the one off DESMOND intervention is cost effective, it must be noted that the DESMOND programme was never intended as a one off intervention. An ongoing model of education and care is currently being developed, which will provide reinforcement at additional points of contact and an optimal environment for improving patient outcomes from education, as discussed by Loveman and colleagues.30 Diabetes prevention trials have shown that with reinforcement, benefits such as weight loss can be sustained over a period of several years in many patients.35
The independent effects of some changes in biomedical and other measures on health related quality of life (and comorbidities) are unknown. For example, the DESMOND programme had a favourable effect on symptoms of depression, as measured by the hospital anxiety and depression (HADS) score. It is likely that this effect would result in some economic benefits beyond the trial that are not included in our results; for example, in terms of reduced use of health care, improved quality of life, or both. In addition, the intervention group also achieved a greater fall in triglyceride concentration at month 12 than the control group (a measure that is not captured within the UKPDS cardiovascular disease risk equations) and a more positive change in illness beliefs about diabetes (although the extent to which this is captured by utility instruments such as the EQ-5D warrants further investigation).
No significant effect of the DESMOND intervention on the amount of time spent with healthcare professionals was observed during the trial. Potentially, improved skills in self care might reduce the need for patients with diabetes to seek advice from NHS professionals, although an increased awareness following participation in the DESMOND programme might help patients make better use of opportunities for advice seeking and more appropriate visits to primary healthcare clinicians, as well as improve compliance with drug and prescribed therapies.
As with other lifestyle programmes, such as those to prevent diabetes, there will be considerable variability across patients in their response to the DESMOND intervention. Greater understanding of how to lessen physiological and motivational barriers in non-responsive individuals would help to improve the effectiveness of the intervention in a broad mix of patients.
The real world costs of delivering the DESMOND programme are likely to vary considerably across primary care trusts. The main variables affecting the cost are the number of educators trained, the grade of healthcare professional delivering courses, venue cost, ratio of demand to head of population (including participation rate), number of patients per course, and overhead rates. There is a continuum of delivery costs associated with delivering the intervention, ranging from running the intervention extremely efficiently (for example, training a small number of educators and having them deliver the DESMOND programme full time) to running it less efficiently (for example, with a high ratio of educators to course sessions). These factors need to be considered when setting up a cost effective DESMOND programme.
We conclude, on the basis of the results of a randomised controlled trial of the intervention and estimated costs of delivery in the real world, that the DESMOND programme is a low cost and likely cost effective intervention for patients with newly diagnosed type 2 diabetes. People attending DESMOND sessions are encouraged to decide on their own goals, which often include weight loss and smoking cessation. These outcomes were both significantly improved in the trial and were the most important drivers in the economic analysis. Although HbA1c level was not improved in the trial of the DESMOND intervention, this may have been because the major improvements in HbA1c level achieved in the period after diagnosis of diabetes, as seen in both study arms, may have masked any effect of the intervention.36 Maintenance of these benefits is important for reducing the risk of cardiovascular disease and improving quality of life. Our analysis indicates that the DESMOND programme is likely to be a cost effective form of structured education that should be given in line with National Institute for Health and Clinical Excellence guidance.5
Contributors: MG carried out the statistical analysis with advice and assistance from MJC, P Fitzgerald, and T Young. MG carried out the economic analysis with advice from SD and AB. HMD, MEC, SH, KK, and MJD assisted with the costing of the intervention. MG wrote the paper with assistance from HMD, SD, AB, MEC, MJC, SH, KK, TCS, and MJD. TCS, SH, MEC, KK, and MJD are the principal investigators of the DESMOND study. All authors had full access to all of the data in the study (including statistical reports and tables) and can take responsibility for the integrity of the data and the accuracy of the data analysis. MG is the guarantor.
Funding: The study was funded by a grant from Diabetes UK secured by the University Hospitals of Leicester NHS Trust. The analysis was independently designed and undertaken by the University of Sheffield School of Health and Related Research and collaborators. Researchers worked independently from the funders. Similarly the writing of the report and the decision to submit the article for publication was entirely independent of the funder. The study funder had no input into the study design or analysis, nor the interpretation of data.
Competing interests: All authors have completed the Unified Competing Interest form at www.icmje.org/coi_disclosure.pdf (available on request from the corresponding author) and declare: no support from any company for the submitted work; no financial relationships with any companies that might have an interest in the submitted work in the previous 3 years; no other relationships or activities that could appear to have influenced the submitted work.
Ethical approval: The study was approved by the Huntingdon local research ethics committee.
Data sharing: No data from the original DESMOND trial is currently available for sharing at this moment in time.
Cite this as: BMJ 2010;341:c4093