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Cost data for individual patients included in clinical studies: no amount of statistical analysis can compensate for inadequate costing methods

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Author Info

  • Nicholas Graves

    (Department of Public Health & Policy, London School of Hygiene & Tropical Medicine, University of London, UK)

  • Damian Walker

    (Department of Public Health & Policy, London School of Hygiene & Tropical Medicine, University of London, UK)

  • Rosalind Raine

    (Department of Public Health & Policy, London School of Hygiene & Tropical Medicine, University of London, UK)

  • Andrew Hutchings

    (Department of Public Health & Policy, London School of Hygiene & Tropical Medicine, University of London, UK)

  • Jennifer A. Roberts

    (Department of Public Health & Policy, London School of Hygiene & Tropical Medicine, University of London, UK)

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    Abstract

    This work examines the quality of the cost methods used to derive patient level costs in 45 economic evaluations conducted alongside randomised controlled trials. The perspective of the cost analysis, the methods used to determine quantities and values of resources and how the cost data were reported are examined. The reported costing methods were found to be of poor quality, highlighting the need for greater rigour. Researchers to date appear more concerned with whether cost data have been subjected to the appropriate statistical analysis. For the results of clinical studies to be valid both cost methods and the methods used for the statistical analysis of cost data should be of a high quality. Copyright © 2002 John Wiley & Sons, Ltd.

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    File URL: http://hdl.handle.net/10.1002/hec.683
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    Bibliographic Info

    Article provided by John Wiley & Sons, Ltd. in its journal Health Economics.

    Volume (Year): 11 (2002)
    Issue (Month): 8 ()
    Pages: 735-739

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    Handle: RePEc:wly:hlthec:v:11:y:2002:i:8:p:735-739

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    Web page: http://www3.interscience.wiley.com/cgi-bin/jhome/5749

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    Cited by:
    1. Gerald Richardson & Andrea Manca, 2004. "Calculation of quality adjusted life years in the published literature: a review of methodology and transparency," Health Economics, John Wiley & Sons, Ltd., vol. 13(12), pages 1203-1210.
    2. Radhakrishnan, Muralikrishnan & van Gool, Kees & Hall, Jane & Delatycki, Martin & Massie, John, 2008. "Economic evaluation of cystic fibrosis screening: A review of the literature," Health Policy, Elsevier, vol. 85(2), pages 133-147, February.
    3. M. Carreras & M. García-Goñi & P. Ibern & J. Coderch & L. Vall-Llosera & J. Inoriza, 2011. "Estimates of patient costs related with population morbidity: can indirect costs affect the results?," The European Journal of Health Economics, Springer, vol. 12(4), pages 289-295, August.
    4. Marion Haas & Marian Shanahan & Rob Anderson, 2007. "Assessing the costs of organised health programs: The case of the National Cervical Screening Program," Working Papers 2007/2, CHERE, University of Technology, Sydney.

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