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Published 20 November 2008, doi:10.1136/bmj.a2097
Cite this as: BMJ 2008;337:a2097
A Sarah Walker, statistician1,2, David Spiegelhalter, professor of the public understanding of risk3,4, Derrick W Crook, consultant microbiologist1, David Wyllie, research fellow5, James Morris, consultant pathologist1, Tim E A Peto, professor of infectious diseases1
1 National Institute for Health Research Oxford Biomedical Research Centre Programme, John Radcliffe Hospital, Oxford OX3 9DU, 2 MRC Clinical Trials Unit, London NW1 2DA, 3 MRC Biostatistics Unit, Institute of Public Health, Cambridge CB2 0SR, 4 Statistical Laboratory, Centre for Mathematical Sciences, Cambridge CB3 0WB, 5 Nuffield Department of Clinical Laboratory Sciences, University of Oxford, Oxford, OX3 9DU
Correspondence to: A S Walker asw{at}ctu.mrc.ac.uk
Trusts in England have been given targets to reduce C difficile infection rates. But Sarah Walker and colleagues argue that the way they are calculated makes financial penalties almost impossible to avoid
Financial incentives are increasingly being used to promote delivery of efficient, high quality health care.1 2 3 However, it is widely agreed that such incentives have to be carefully constructed, with clear and simple links between behaviours or outcomes and incentives, direct indicators that validly measure the desired behaviours or outcomes, and sufficient stability to give surety to hospitals that effort (time, money) put into achieving targets is warranted.1 3 We examine how well these criteria are met by the financial penalties introduced for failing to reduce hospital acquired Clostridium difficile infection as part of the 2008-9 standard National Health Service contract for acute services.
In response to a new hypervirulent strain of C difficile causing large hospital outbreaks since 2003,4 5 the Department of Health recently set a target of a 30% reduction in C difficile infections in patients aged 2 years or older across the entire health economy (within and outside acute NHS trusts) from 2007-8 to 2010-11.6 All financial penalties relating to this target are based on comparing the number of cases observed in the current "contract year" to the number of cases observed in the previous "baseline" financial year. If 200 or more cases are observed in the baseline or contract year, the penalty is based on failing to meet the target reduction in the contract year (0.2% of total contract year revenue for every percentage point the target is underachieved, capped at 2% when target underachieved by 10%). However, if fewer than 200 cases are observed in the baseline and contract year, the penalty is based on exceeding the number of baseline cases (0.1% for every percentage point increase or 0.05% if baseline is below 50 cases, capped at 2% when there has been a 20% or 40% increase over baseline respectively).
Targets will be set by primary care trusts, which commission services from hospital trusts. Assuming, for simplicity, that the average target reduction is 10% a year, the financial penalties follow the trajectories in fig 1
. Although the penalty is capped at 2% of income, the amounts of money are not trivial. A large trust would have a contract revenue of around £500m (
600m; $750m), and thus a 2% penalty would be £10m and even 0.1% would be £500 000, the equivalent of 10 mid-grade nurses.
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Suppose that a trust strengthens or introduces practices believed to improve C difficile control, such as enhanced cleaning with 10% sodium hypochlorite, use of barrier precautions, thorough handwashing with chlorhexidine or soap and water, and changes in antibiotic policies.8 9 10 11 The expected financial penalty will depend on three factors:
The key point is that C difficile infection is not under a hospitals complete control. C difficile infection occurs relatively rarely (around 2-3 cases/1000 days among hospital patients aged over 657) but has very many opportunities to happen. Therefore the number of cases observed is subject to considerable natural random variation; if the true risk reduction is 10%, the observed reduction is equally likely to be above or below that figure (fig 2
). In this situation, the only way to estimate expected penalties is by simulating cases in a baseline year and various true reductions or increases in C difficile risk across three further years and then calculating the average financial penalties. We simulated the consequences of various genuine reductions in C difficile risk (from a 20% reduction to a 10% increase) across four years of observation, with the expected number of cases in the baseline year ranging from 25 to 1000, and estimated the financial penalties over one and three years, assuming that the target is a 10% annual reduction. We repeated each simulation 50 000 times. Poisson distributions were assumed for count data: these assume independent observations in each year and in practice there is considerable clustering of cases leading to substantial volatility from year to year. For example, between 2004 and 2007, the median coefficient of variation (standard deviation divided by mean) of the annual C difficile counts for people over 65 was 0.21: this "average volatility" was represented by Swindon and Marlborough Trust, which had 246, 230, 349, and 322 cases. This extra-Poisson variability means that our estimates can therefore be assumed to be conservative.
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, on which the width of the sampling distribution in the contract year is based, goes up. To have a small (<5%) chance of not paying any financial penalty under the formulas for a 10% target, trusts will have to exceed the target by 5-15% (fig 4
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Thus the 98 (58%) trusts with more than 250 cases in 2007-8 that believe they can achieve the target risk reductions should still reserve 0.4-0.6% total contract revenue for financial penalties; those that do not think they can achieve this should probably reserve the full 2%.
The stipulated financial penalties implicitly assume that rates of C difficile infections can be estimated precisely enough to know that an observed 1-10% underachievement of target is actually a true underachievement. This simply does not hold: observed underachievements may merely be an artefact of variability in the observed rate reduction. This variability is increased by using a single baseline year, leading to the well known statistical problem regression to the mean.12 13 14 If the number of baseline cases observed happens to be high by chance, the number of cases in the following year is likely to be lower just because getting two random high observations is less likely. Similarly, if the number of observed baseline cases is low by chance, the number in the next year is likely to be closer to or higher than average (fig 2
). For example, Taunton and Somerset NHS Trusts figures for people aged over 65 between 2004 and 2007 are 331, 399, 409, 173, suggesting that the recent reduction may be at least partly due to chance, and giving them an extremely challenging first baseline year. Although both situations are equally likely, the financial penalties work in only one direction, with only chance low numbers followed by natural highs being penalised harshly.
Unfortunately, the rolling baseline year maximises the cumulative impact of regression to the mean over three years. Even if the true underlying risk is going down according to target, sampling error means it is highly likely that the cases observed will lie above the expected trajectory at least once in three years and thus a financial penalty will be paid at least once. In fact, if the target is a 10% annual reduction, 95% of trusts with 250-1000 baseline cases and a true 10% annual risk reduction would pay a financial penalty at least once over three years (fig 5
). Trusts would have to reduce risk by 10-15% more than the target to have a less than 5% chance of paying a penalty over the three years (fig 6
). As an example, East Sussex Hospitals NHS Trust had 393, 387, 374, and 303 cases in people aged over 65 in successive years from 2004 to 2007—if such a penalty scheme had been in place they would have paid a penalty in two of the three years owing to not achieving a 10% reduction, despite an observed reduction of 30% between the baseline year of 2004 and 2007.
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Figure 7
can be used to estimate the probability of paying a financial penalty and the mean financial penalty incurred over one and three contract years for trusts with various numbers of baseline cases according to different reductions in risk of C difficile infection. Although our simulations assume a 10% annual target reduction, the results generalise to different targets as they are based on well known statistical properties such as sampling variability and regression to the mean. It is clear that achieving the required target is not predictably linked to avoidance of severe financial penalties.
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If investing effort to achieve the required target does not predictably avoid penalty, it may be more efficient simply to accept the penalty.1 Trusts will have to balance the costs and feasibility of achieving large enough real reductions in C difficile infections to minimise the chance that their observed reduction will not incur a penalty against the costs of merely accepting the penalty whether or not they have truly achieved the required target. We believe the current approach runs a serious risk of demotivating trusts, since they stand a 50% chance of being penalised in any one year even if they achieve target reductions in risk and are almost certain to be penalised at least once in three years, just as a consequence of natural random variation.
Given this natural variation, identifying a financial penalty scheme with high specificity (a high chance of penalising trusts not achieving target) and high sensitivity (high chance of not penalising trusts achieving target) is impossible. We therefore consider that a fairer financial penalty would aim for consistently high sensitivity—that is, it should have a low chance of penalising trusts whose observed cases are compatible with the target risk reduction, allowing for natural random variation. It should not use a single year as a baseline nor a rolling baseline year, as this maximises regression to the mean effects, and it should not differentially penalise trusts with different baseline number of cases but the same relative risk reduction.
One proposal would be to estimate a baseline number of cases for each trust using the mean across the last three years. Although this involves some estimation because relevant data were not collected in all subgroups throughout this period,7 it will at least reduce variation in the major subgroup of over 65s in hospital. From this baseline, expected target reductions could be calculated for the next three years, and 90th or 95th percentiles around these designated a breach. The Healthcare Commission recommends and uses this approach.15 Trusts with observed cases above the breach level could be penalised by various degrees according to their tail probability for the expected sampling distribution. For example, for an average trust with a mean of 300 cases a year during 2005-7, successive 10% annual reductions would be 270, 243, and 219 cases a year. The 90th (95th) percentiles sampled from these expected reductions are 291 (297), 263 (269), and 238 (244) respectively. Penalising observed numbers of cases above these levels would approximate sensitivity of 90% or 95%.
Even if such a financial penalty achieved the presumed goal of encouraging NHS trusts to make the C difficile target one of their highest priorities, a major question remains as to its actual effect on service provision. End of year penalties mean money has to be put aside and not spent on services during a financial year to ensure that fines can be paid at the end of it. Furthermore, primary care trusts will receive large sums of money from these penalties at the end of each financial year, which will then have to be disposed of in some (as yet undetermined) way. Financial targets, particularly as implemented in the current NHS contract for acute services, may therefore have unexpected and unwanted effects on the smooth running of trusts, other than achieving the primary aims of much needed reductions in outcomes such as C difficile infections.
Cite this as: BMJ 2008;337:a2097
Funding: This project was funded as part of the National Institute for Health Research Oxford Biomedical Research Centre Programme.
Competing interests: None declared.
Provenance and peer review: Not commissioned; externally peer reviewed.
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