How should cost data in pragmatic randomised trials be analysed?
BMJ 2000; 320 doi: https://doi.org/10.1136/bmj.320.7243.1197 (Published 29 April 2000) Cite this as: BMJ 2000;320:1197 Simon G Thompson, professor (simon.thompson{at}mrcbsu.cam.ac.uk),
 Julie A Barber, research fellow
 Department of Medical Statistics and Evaluation, Imperial College School of Medicine, London W12 0NN
 Correspondence to: S G Thompson, MRC Biostatistics Unit, Institute of Public Health, Cambridge CB2 2SR
 Accepted 13 December 1999
Pragmatic randomised trials are usually large scale multicentre studies in which interventions or medical policies are compared in a realistic setting.1 The intention is that conclusions from these trials, if accepted, can be adopted directly into medical practice.2 Economic evaluations carried out alongside these trials are increasingly common because it is often important to assess costs and cost effectiveness as well as clinical outcomes.3 Costs are usually derived from information about the quantity of healthcare resources used by each patient in the trial. The quantities of each resource used are multiplied by fixed unit cost values and are then summed over the separate types of resource to give a total cost per patient.4
This information leads to a range of different costs across participants in the trial. As an example, the figure shows the distribution of costs in women with menorrhagia randomised to treatment with endometrial resection or abdominal hysterectomy.5 Such highly skewed distributions are typical of cost data; the long right hand tail reflects the fact that some patients incur high costs because of factors such as medical complications, reoperation, or extended hospital stay.
Summary points
Health economic evaluations are now commonly included in pragmatic clinical trials that inform policy decisions
Despite the usual skewness in the distribution of costs, it is the arithmetic mean that is the most informative measure
Measures other than the arithmetic mean do not provide information about the cost of treating all patients, which is needed as the basis for healthcare policy decisions
Statistical analysis based on transforming cost data or comparing medians using standard nonparametric methods may provide misleading conclusions
What aspect of cost data is important?
When information about the costs of alternative treatments is to be used to guide healthcare policy decision making, it is the total budget needed to treat patients with the disease that is relevant. For example, healthcare planners may need information about the total annual budget required to provide a treatment at a particular hospital. An estimate of this total cost is obtained from data in a trial by multiplying the arithmetic mean (average) cost in a particular treatment group by the total number of patients to be treated. It is therefore the arithmetic mean that is the informative measure for cost data in pragmatic clinical trials.
Other measures, however, are often reported when describing cost data. For example, the median cost is the value below and above which the costs of half the patients lie. Another measure, the geometric mean cost, can be derived by transforming the costs onto a logarithmic scale, calculating the average, and transforming this back. For positively skewed data such as those in the figure, the median and geometric mean are always less than the arithmetic mean. For example, in the endometrial resection group, the median cost was £523, the geometric mean was £683, and the arithmetic mean was £790. The extent of differences between these quantities depends on the shape and skewness of the distribution. Hence, in the hysterectomy group, in which cost data are less skewed, the median of £1053 and the geometric mean of £1100 are closer to the arithmetic mean of £1110.
Measures other than arithmetic means may be useful for some purposes. For example, the median cost may be used to describe a “typical” cost for an individual. Knowledge of the probability of incurring a particularly extreme cost may be useful to a medical insurance company. Measures other than the arithmetic mean, however, do not provide information about the total cost that will be incurred by treating all patients, which is needed as the basis for healthcare policy decisions.
How should costs be compared?
Many commonly used statistical methods require that data approximate a symmetrical bell shaped—or normal—distribution. Researchers have therefore chosen statistical techniques which try to deal with the skewness in the distribution of cost data. At first sight this is reasonable, given the advice in statistical guidelines and textbooks. For example, the BMJ's statistical guidelines state that “data which have a highly skewed (asymmetrical) distribution …may require either some transformation before analysis or the use of alternative ‘distribution free’ methods.”6 A transformation of the data, such as a logarithmic transformation, might be used to achieve a more normal distribution, for which “parametric” methods such as a t test are appropriate. Alternatively, “nonparametric” or distribution free methods, which are appropriate for any shape of distribution, could be used.
This conventional advice implies that the method of analysis should be chosen on the basis of the shape of the distribution of the data. However, the method of analysis used also has important implications for the interpretation of results, since different methods compare different aspects of the distributions. A t test on untransformed data compares arithmetic means, while a t test on log transformed data compares geometric means. The MannWhitney U test, a nonparametric method, is often interpreted as a comparison of medians, although it is in fact an overall comparison of distributions in terms of both shape and location.7 Out of these three tests, only the t test on untransformed data can be appropriate for costs, since it is the only one that addresses a comparison of arithmetic means. A legitimate concern, and the basis of the conventional statistical guidelines, is that methods based on the t test are strictly valid only if the cost data are normally distributed.8 However, a t test, and the confidence interval derived from it, will be reliable if either the skewness is not too extreme or the sample sizes are moderately large—an issue to which we return later.
Examples from three recent publications
In a pragmatic randomised trial comparing hospital at home with inpatient hospital care, the strategy for statistical analysis was as follows: “When appropriate, data with nonnormal distributions was log transformed before further parametric analysis was done. The MannWhitney U test was used for continuous data that did not approximate a normal distribution after log transformation.”9 The table shows the result of this strategy for the group of hip replacement patients included in the trial. Arithmetic mean hospital costs were compared by using a t test, general practitioner costs were presented as medians and compared with a MannWhitney U test, and, although total costs were presented as arithmetic means, geometric means were compared statistically by using an analysis based on log transformed values. The confusion over methods of analysis and their resulting presentation is obvious. It stems, however, from following the conventional guidelines for the statistical analysis of continuous data. In addition, presenting arithmetic means while comparing geometric means statistically (which was, it seems, recommended recently10) can only encourage misinterpretation.
In a second example, a pragmatic randomised trial was carried out to assess the cost effectiveness over one year of day hospital compared with inpatient treatment for patients with acute psychiatric illness.11 Because the cost data were skewed, the authors used medians to summarise the distributions and the MannWhitney U test to make comparisons between groups. This analysis showed that total patient costs were statistically significantly lower in the day hospital group. It does not follow, however, that the arithmetic mean costs were also significantly lower. So the authors' conclusion that day hospital treatment was cheaper overall, which has direct policy implications, is not justified by the statistical analysis presented.
A similar example is provided by a pragmatic randomised trial evaluating care for discharged psychiatric patients. In this study, community multidisciplinary teams and hospital based care over one year were compared.12 Arithmetic mean, median, and geometric mean costs were presented, but only the geometric mean costs were compared statistically, using a t test on log transformed values “to correct for skewed distribution.” As for medians in the previous example, the nonsignificant difference in geometric mean costs cannot be taken to imply a similar result for arithmetic mean costs.
Does the choice of method matter?
In these examples, it is not clear whether using a comparison of arithmetic means would have changed the conclusions. The reader cannot be sure and cannot therefore draw reliable conclusions from the analyses presented. As the necessary analyses can readily be performed when original data are available, it is easy to find examples to show that the choice of method of analysis can make a difference to the conclusions. In a trial comparing a community based exercise programme and usual general practitioner care for patients with low back pain, the arithmetic mean costs over 12 months were £360 and £508 respectively.13 Using t test based methods to assess the mean difference of £148 gave a 95% confidence interval of −£146 to £442 and a nonsignificant P value of 0.32, thus providing no evidence of a difference. However, a MannWhitney U test applied to the same data gave a significant P value of 0.02, which would be interpreted as substantial evidence of a cost difference. Clearly, these two methods lead to very different interpretations for the cost evaluation, and if the MannWhitney U test had been used it would have been extremely misleading.
Another example is provided by the subgroup of hysterectomy patients included in the hospital at home trial described above.9 It was stated that in this case “health service costs were significantly higher for those allocated to hospital at home care.” The conclusion was based on a comparison of geometric means, the cited P value being <0.01. However, using the arithmetic means and standard deviations reported in the paper to carry out a standardt test gives a less significant P value of 0.1. Again, these two analyses lead to different interpretations.
How common are these problems?
A recent review of 45 randomised trials that included economic evaluations and were published in 1995 showed serious inadequacies in the use of statistical methods for costs.14 Among the papers that reported statistical comparisons, only half used methods that addressed differences in arithmetic means, and others used inappropriate nonparametric approaches (for example, MannWhitney U test) or log transformation approaches. The situation is made worse by recent articles giving incorrect or misleading advice about the statistical analysis of cost data. Although it has been mentioned that standard nonparametric methods are inappropriate, several authors have (wrongly) recommended carrying out analyses on log transformed cost data.15^{–}18 These recommendations have influenced methods of analysis used in subsequent studies.19 In the context of cost data, the unthinking application of conventional statistical guidelines for analysing skewed data leads to inappropriate analyses and potentially misleading conclusions.
Appropriate methods of analysis
Given the need to compare treatment groups in terms of arithmetic mean costs, standard approaches such as t tests seem to be appropriate. Indeed, in the review of published economic evaluations, ttests were used for all the comparisons of arithmetic means reported.14 Their validity, however, relies on assumptions of “normality” and so is questionable for skewed cost data.8 Although these methods are known to be fairly robust to nonnormality, especially if the sample size is large, robustness for a particular data set is difficult to judge.7 Standard methods for comparing arithmetic mean costs therefore may have to be used with caution.
One alternative approach is the nonparametric bootstrap.20 This method avoids the need to make assumptions about the shape of the distribution, such as normality, and uses instead the observed distributions of the cost data in the study being analysed. Statistical analysis is based on repeatedly sampling from the observed data, using a computer program.21 Bootstrap methods can be used for hypothesis tests, calculating confidence intervals and regression analyses. The application of the nonparametric bootstrap to test and derive confidence intervals for differences in arithmetic mean costs has recently been described.21 22 As yet, bootstrap methods have not often been used for analysing costs in practice, although there are some recent examples.13 23^{–}25
In our experience, the results from standard t tests and t test based confidence intervals are adequate in most realistic situations for comparing arithmetic mean costs between two groups. For cost data in general, we prefer methods that do not assume that the standard deviations in the two groups are the same.26 For example, in the menorrhagia trial (see figure), the 95% confidence intervals for the difference in arithmetic mean costs between groups (£320) were very similar whether a t test based method or bootstrap method was used (£204 to £437 and £192 to £426, respectively). This is despite the skewness of the cost data, especially in the endometrial resection group, and the moderate number of patients in each group (78 and 70). Even with lower sample sizes of about 1520 patients per group and highly skewed cost data, results can be similar. For example, in a pilot trial of cognitive behavioural therapy for patients with deliberate self harm, P values for the t test and a bootstrap test were almost identical (0.20 and 0.21 respectively) and the methods again gave fairly similar confidence intervals.23
Conclusions
In cost evaluations designed to have an impact on medical policy, it is the total healthcare cost that is important. Thus, despite the usually skewed distribution of cost data, it is analyses of arithmetic means that are informative. A simple t test of untransformed costs may be sufficient, but the validity of these results, especially for small samples or extremely skewed data, should be checked by using bootstrap techniques. There is a need for economic and statistical guidelines to be revised to emphasise these issues, since basing important policy decisions on studies that use inappropriate methods of analysis for costs may do more harm than good.
Acknowledgments
We thank Mark Sculpher and colleagues and Jennifer Klaber Moffett and colleagues for permission to use data from their studies.
Footnotes

Funding ST was funded by HEFC London University, JB by Thames NHS Executive.

Competing interests None declared.