Paper

International Journal of Obesity (2005) 29, 517–523. doi:10.1038/sj.ijo.0802925 Published online 1 March 2005

Orlistat in responding obese type 2 diabetic patients: meta-analysis findings and cost-effectiveness as rationales for reimbursement in Sweden and Switzerland

J Ruof1,2, A Golay3, C Berne4, C Collin5, J Lentz6 and A Maetzel7

  1. 1Health Services Research Unit, Division of Rheumatology, Center of Internal Medicine, Hannover Medical School, Hannover, Germany
  2. 2Global Health Economics Department, Roche Pharmaceuticals, Basel, Switzerland
  3. 3Teaching Diabetic Division, University Hospital, Geneva, Switzerland
  4. 4Department of Medicine, University Hospital, Uppsala, Sweden
  5. 5Business Development, Roche Pharmaceuticals, Stockholm, Sweden
  6. 6Roche Pharmaceuticals, Reinach, Switzerland
  7. 7University Health Network, Department of Health Policy Management and Evaluation, University of Toronto, Toronto, Ontario, Canada

Correspondence: Dr DJ Ruof, Division of Rheumatology, Hannover Medical School, Carl-Neuberg-Str. 1, D-30625 Hannover, Germany. E-mail: joerg.ruof@roche.com

Received 4 February 2004; Revised 10 December 2004; Accepted 16 January 2005; Published online 1 March 2005.

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Abstract

OBJECTIVE:

 

The aim of this study is to review the clinical and economic rationale for the reimbursement of orlistat in responding obese patients with type 2 diabetes.

METHODS:

 

Data from seven randomized controlled clinical trials of orlistat in overweight and obese patients with type 2 diabetes were pooled. A subgroup analysis involving patients who achieved a response (defined as a weight loss of greater than or equal to5% after 12 weeks of treatment) was conducted. The outcomes of the pooled analysis were then used to construct a Markov health economic model covering an 11-y period. The incidences of diabetes-related micro- and macrovascular complications were derived from the United Kingdom Prospective Diabetes Study. The effects of changes in body mass index, and the impact of micro- and macrovascular complications on utilities were derived from published sources. Publicly available cost data were used and are presented here in 2001 Euros. Discounting of 3% was applied. A probabilistic sensitivity analysis was conducted to examine the robustness of results.

RESULTS:

 

A total of 1249 patients treated with orlistat and 1230 given placebo were eligible for the intent-to-treat analysis. At the end of the study period, 23% of orlistat patients achieved a weight reduction of greater than or equal to5%. These patients showed a mean decrease in HbA1C of 1.16%, a weight reduction of 8.6 kg, a reduction in total cholesterol of 5.3% and a reduction in systolic blood pressure of 5.2 mmHg. The base-case economic analysis revealed costs per quality-adjusted life year gained of euro dollar14 000 in Sweden and euro dollar13 600 in Switzerland.

CONCLUSION:

 

The data presented here support the utilization and reimbursement of orlistat in overweight and obese diabetic patients who respond to the treatment.

Keywords:

orlistat, cost-effectiveness, diabetes, reimbursement, meta-analysis

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