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Predicting the Cost of Illness

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  • Joseph Lipscomb
  • Marek Ancukiewicz
  • Giovanni Parmigiani
  • Vic Hasselblad
  • Greg Samsa
  • David B. Matchar

Abstract

Predictions of cost over well-defined time horizons are frequently required in the anal ysis of clinical trials and social experiments, for decision models investigating the cost-effectiveness of interventions, and for macro-level estimates of the resource im pact of disease. With rare exceptions, cost predictions used in such applications con tinue to take the form of deterministic point estimates. However, the growing availability of large administrative and clinical data sets offers new opportunities for a more general approach to disease cost forecasting: the estimation of multivariable cost functions that yeld predictions at the individual level, conditional on intervention(s), patient charac teristics, and other factors. This raises the fundamental question of how to choose the "best" cost model for a given application. The central purpose of this paper is to demonstrate how to evaluate competing models on the basis of predictive validity. This concept is operationalized according to three alternative criteria: 1) root mean square error (RMSE), for evaluating predicted mean cost; 2) mean absolute error (MAE), for evaluating predicted median cost; and 3) a logarithmic scoring rule (log score), an information-theoretic index for evaluating the entire predictive distribution of cost. To illustrate these concepts, the authors conducted a split-sample analysis of data from a national sample of Medicare-covered patients hospitalized for ischemic stroke in 1991 and followed to the end of 1993. Using test and training samples of about 500,000 observations each, they investigated five models: single-equation linear models, with and without log transform of cost; two-part (mixture) models, with and without log transform, to directly address the problem of zero-cost observations; and a Cox pro portional-hazards model stratified by time interval. For deriving the predictive distri bution of cost, the log transformed two-part and proportional-hazards models are su perior. For deriving the predicted mean or median cost, these two models and the commonly used log-transformed linear model all perform about the same. The untrans formed models are dominated in every instance. The approaches to model selection illustrated here can be applied across a wide range of settings. Key words: cost anal ysis ; cost of illness; statistical models; econometric models; stroke; cerebrovascular disease. (Med Decis Making 1998;18 suppl:S39-S56)

Suggested Citation

  • Joseph Lipscomb & Marek Ancukiewicz & Giovanni Parmigiani & Vic Hasselblad & Greg Samsa & David B. Matchar, 1998. "Predicting the Cost of Illness," Medical Decision Making, , vol. 18(2_suppl), pages 39-56, April.
  • Handle: RePEc:sae:medema:v:18:y:1998:i:2_suppl:p:s39-s56
    DOI: 10.1177/0272989X98018002S07
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    References listed on IDEAS

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    1. Fenn, Paul & McGuire, Alistair & Backhouse, Martin & Jones, David, 1996. "Modelling programme costs in economic evaluation," Journal of Health Economics, Elsevier, vol. 15(1), pages 115-125, February.
    2. Manning, Willard G, et al, 1987. "Health Insurance and the Demand for Medical Care: Evidence from a Randomized Experiment," American Economic Review, American Economic Association, vol. 77(3), pages 251-277, June.
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    1. Christian Kronborg Andersen & Kjeld Andersen & Per Kragh‐Sørensen, 2000. "Cost function estimation: the choice of a model to apply to dementia," Health Economics, John Wiley & Sons, Ltd., vol. 9(5), pages 397-409, July.
    2. Maria Raikou & Alistair McGuire, 2012. "Estimating Costs for Economic Evaluation," Chapters, in: Andrew M. Jones (ed.), The Elgar Companion to Health Economics, Second Edition, chapter 43, Edward Elgar Publishing.
    3. Norman J. Waitzman & Patrick S. Romano & Scott D. Grosse, 2004. "The Half-Life of Cost-of-Illness Estimates: The Case of Spina Bifida," Working Paper Series, Department of Economics, University of Utah 2004_07, University of Utah, Department of Economics.
    4. Frank A. Sloan & Gabriel A. Picone & Donald H. Taylor, Jr. & Shin-Yi Chou, 1999. "Does Where You Are Admitted Make a Difference? An Analysis of Medicare Data," NBER Chapters, in: Frontiers in Health Policy Research, volume 2, pages 1-26, National Bureau of Economic Research, Inc.
    5. Basu A & Manning WG, 2009. "Estimating Lifetime or Episode-of-illness Costs," Health, Econometrics and Data Group (HEDG) Working Papers 09/12, HEDG, c/o Department of Economics, University of York.
    6. Johnson, Elizabeth & Dominici, Francesca & Griswold, Michael & L. Zeger, Scott, 2003. "Disease cases and their medical costs attributable to smoking: an analysis of the national medical expenditure survey," Journal of Econometrics, Elsevier, vol. 112(1), pages 135-151, January.
    7. M. Raikou & A. Briggs & A. Gray & A. McGuire, 2000. "Centre‐specific or average unit costs in multi‐centre studies? Some theory and simulation," Health Economics, John Wiley & Sons, Ltd., vol. 9(3), pages 191-198, April.
    8. Anirban Basu & Willard G. Manning & John Mullahy, 2004. "Comparing alternative models: log vs Cox proportional hazard?," Health Economics, John Wiley & Sons, Ltd., vol. 13(8), pages 749-765, August.
    9. Borislava Mihaylova & Andrew Briggs & Anthony O'Hagan & Simon G. Thompson, 2011. "Review of statistical methods for analysing healthcare resources and costs," Health Economics, John Wiley & Sons, Ltd., vol. 20(8), pages 897-916, August.

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