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Cost-effectiveness of pioglitazone in type 2 diabetes patients with a history of macrovascular disease: a German perspective
BACKGROUND: The aim of this study was to project health-economic outcomes relevant to the German setting for the addition of pioglitazone to existing treatment regimens in patients with type 2 diabetes, evidence of macrovascular disease and at high risk of cardiovascular events. METHODS: Event rates...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688482/ https://www.ncbi.nlm.nih.gov/pubmed/19416529 http://dx.doi.org/10.1186/1478-7547-7-9 |
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author | Scherbaum, Werner A Goodall, Gordon Erny-Albrecht, Katrina M Massi-Benedetti, Massimo Erdmann, Erland Valentine, William J |
author_facet | Scherbaum, Werner A Goodall, Gordon Erny-Albrecht, Katrina M Massi-Benedetti, Massimo Erdmann, Erland Valentine, William J |
author_sort | Scherbaum, Werner A |
collection | PubMed |
description | BACKGROUND: The aim of this study was to project health-economic outcomes relevant to the German setting for the addition of pioglitazone to existing treatment regimens in patients with type 2 diabetes, evidence of macrovascular disease and at high risk of cardiovascular events. METHODS: Event rates corresponding to macrovascular outcomes from the Prospective Pioglitazone Clinical Trial in Macrovascular Events (PROactive) study of pioglitazone were used with a modified version of the CORE Diabetes Model to simulate outcomes over a 35-year time horizon. Direct medical costs were accounted from a healthcare payer perspective in year 2005 values. Germany specific costs were applied for patient treatment, hospitalization and management. Both costs and clinical benefits were discounted at 5.0% per annum. RESULTS: Over patient lifetimes pioglitazone treatment improved undiscounted life expectancy by 0.406 years and improved quality-adjusted life expectancy by 0.120 quality-adjusted life years (QALYs) compared to placebo. Direct medical costs (treatment plus complication costs) were marginally higher for pioglitazone treatment and calculation of the incremental cost-effectiveness ratio (ICER) produced a value of €13,294 per QALY gained with the pioglitazone regimen versus placebo. Acceptability curve analysis showed that there was a 78.2% likelihood that pioglitazone would be considered cost-effective in Germany, using a "good value for money" threshold of €50,000 per QALY gained. Sensitivity analyses showed that the results were most sensitive to changes in the simulation time horizon. After adjustment for the potential stabilization of pancreatic β-cell function with pioglitazone treatment, the ICER was €6,667 per QALY gained for pioglitazone versus placebo. CONCLUSION: The findings of this modelling analysis indicated that, for patients with a history of macrovascular disease, addition of pioglitazone to existing therapy reduces the long-term cumulative incidence of diabetes-complications at a cost that would be considered to represent good value for money in the German setting. |
format | Text |
id | pubmed-2688482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26884822009-05-30 Cost-effectiveness of pioglitazone in type 2 diabetes patients with a history of macrovascular disease: a German perspective Scherbaum, Werner A Goodall, Gordon Erny-Albrecht, Katrina M Massi-Benedetti, Massimo Erdmann, Erland Valentine, William J Cost Eff Resour Alloc Research BACKGROUND: The aim of this study was to project health-economic outcomes relevant to the German setting for the addition of pioglitazone to existing treatment regimens in patients with type 2 diabetes, evidence of macrovascular disease and at high risk of cardiovascular events. METHODS: Event rates corresponding to macrovascular outcomes from the Prospective Pioglitazone Clinical Trial in Macrovascular Events (PROactive) study of pioglitazone were used with a modified version of the CORE Diabetes Model to simulate outcomes over a 35-year time horizon. Direct medical costs were accounted from a healthcare payer perspective in year 2005 values. Germany specific costs were applied for patient treatment, hospitalization and management. Both costs and clinical benefits were discounted at 5.0% per annum. RESULTS: Over patient lifetimes pioglitazone treatment improved undiscounted life expectancy by 0.406 years and improved quality-adjusted life expectancy by 0.120 quality-adjusted life years (QALYs) compared to placebo. Direct medical costs (treatment plus complication costs) were marginally higher for pioglitazone treatment and calculation of the incremental cost-effectiveness ratio (ICER) produced a value of €13,294 per QALY gained with the pioglitazone regimen versus placebo. Acceptability curve analysis showed that there was a 78.2% likelihood that pioglitazone would be considered cost-effective in Germany, using a "good value for money" threshold of €50,000 per QALY gained. Sensitivity analyses showed that the results were most sensitive to changes in the simulation time horizon. After adjustment for the potential stabilization of pancreatic β-cell function with pioglitazone treatment, the ICER was €6,667 per QALY gained for pioglitazone versus placebo. CONCLUSION: The findings of this modelling analysis indicated that, for patients with a history of macrovascular disease, addition of pioglitazone to existing therapy reduces the long-term cumulative incidence of diabetes-complications at a cost that would be considered to represent good value for money in the German setting. BioMed Central 2009-05-05 /pmc/articles/PMC2688482/ /pubmed/19416529 http://dx.doi.org/10.1186/1478-7547-7-9 Text en Copyright © 2009 Scherbaum et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Scherbaum, Werner A Goodall, Gordon Erny-Albrecht, Katrina M Massi-Benedetti, Massimo Erdmann, Erland Valentine, William J Cost-effectiveness of pioglitazone in type 2 diabetes patients with a history of macrovascular disease: a German perspective |
title | Cost-effectiveness of pioglitazone in type 2 diabetes patients with a history of macrovascular disease: a German perspective |
title_full | Cost-effectiveness of pioglitazone in type 2 diabetes patients with a history of macrovascular disease: a German perspective |
title_fullStr | Cost-effectiveness of pioglitazone in type 2 diabetes patients with a history of macrovascular disease: a German perspective |
title_full_unstemmed | Cost-effectiveness of pioglitazone in type 2 diabetes patients with a history of macrovascular disease: a German perspective |
title_short | Cost-effectiveness of pioglitazone in type 2 diabetes patients with a history of macrovascular disease: a German perspective |
title_sort | cost-effectiveness of pioglitazone in type 2 diabetes patients with a history of macrovascular disease: a german perspective |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688482/ https://www.ncbi.nlm.nih.gov/pubmed/19416529 http://dx.doi.org/10.1186/1478-7547-7-9 |
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