A Health Economic Model to Assess the Long-Term Effects and Cost-Effectiveness of Orlistat in Obese Type 2 Diabetic Patients

  1. Mark Lamotte, MD1,
  2. Lieven Annemans, PHD12,
  3. Aurelia Lefever, MD3,
  4. Myriam Nechelput, MSC3 and
  5. Johan Masure, MD3
  1. 1Health Economics and Disease Management, Meise, Belgium
  2. 2University of Ghent, Ghent, Belgium
  3. 3Roche Pharmaceuticals, Brussels, Belgium

    Abstract

    OBJECTIVES—Obesity is a common condition in type 2 diabetic patients. Treating obesity may enhance hypoglycemic treatment and contribute to the reduction of long-term microvascular and macrovascular complications. Orlistat reduces cardiovascular risk factors in obese type 2 diabetic patients. The objectives of this study were to estimate the long-term clinical consequences of this weight loss and the resulting cost-effectiveness of treating obese type 2 diabetic patients with orlistat.

    RESEARCH DESIGN AND METHODS—A Markov model was developed to predict, over a 10-year period, the complication rates and mortality with and without a 2-year orlistat treatment, assuming a 5-year catch-up period after treatment. A stepwise approach was used to obtain the clinical data. First, the impact of weight loss with orlistat on HbA1c, blood pressure, and cholesterol was assessed; then, the impact on mortality and micro- and macrovascular complications of decreasing these risk factors was applied. Four subgroups were studied based on the presence of risk factors.

    RESULTS—Cost-effectiveness varies between 3,462 Euro/life-year gained (LYG) for obese diabetic patients with hypertension and hypercholesterolemia and 19,986 Euro/LYG for obese diabetic patients without other risk factors. The latter result is not robust according to sensitivity analyses.

    CONCLUSIONS—Our results suggest that orlistat is cost-effective in the management of obese type 2 diabetic patients, especially in those with the presence of hypercholesterolemia and/or hypertension. Evidence on longer-term benefits of orlistat (>2 years) will be of importance for future decision-making.

    Footnotes

    • Address correspondence and reprint requests to Lieven Annemans, Brusselsesteenweg 91, B-1860 Meise, Belgium. E-mail: lieven.annemans{at}hedm.be.

      Received for publication 13 June 2001 and accepted in revised form 24 October 2001.

      L.A. has received honoraria from Roche Belgium.

      A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

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