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IDegLira Versus Insulin Glargine U100: A Long-term Cost-effectiveness Analysis in the US Setting
INTRODUCTION: Treatment with IDegLira has the potential to improve glycemic control in patients with type 2 diabetes mellitus (T2DM) without the weight gain and with a lower risk of hypoglycemia than with other therapies. The aim of the present analysis was to evaluate the long-term cost-effectivene...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Healthcare
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446378/ https://www.ncbi.nlm.nih.gov/pubmed/28349444 http://dx.doi.org/10.1007/s13300-017-0251-x |
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author | Hunt, Barnaby Mocarski, Michelle Valentine, William J. Langer, Jakob |
author_facet | Hunt, Barnaby Mocarski, Michelle Valentine, William J. Langer, Jakob |
author_sort | Hunt, Barnaby |
collection | PubMed |
description | INTRODUCTION: Treatment with IDegLira has the potential to improve glycemic control in patients with type 2 diabetes mellitus (T2DM) without the weight gain and with a lower risk of hypoglycemia than with other therapies. The aim of the present analysis was to evaluate the long-term cost-effectiveness of IDegLira versus insulin glargine U100 with re-education and up-titration of the dose for treatment of patients with T2DM failing to achieve glycemic control on basal insulin in the US setting. METHODS: Data were obtained from the DUAL V randomized controlled trial in which adults with T2DM failing to achieve glycemic targets with insulin glargine U100 were randomly allocated to receive either IDegLira or insulin glargine U100. Long-term projections of clinical outcomes and direct costs were made using the IMS CORE Diabetes Model. Costs were accounted from a healthcare payer perspective. Future costs and clinical benefits were discounted at 3% annually. RESULTS: IDegLira was associated with improved discounted life expectancy (13.99 [standard deviation 0.19] versus 13.82 [standard deviation 0.20] years) and quality-adjusted life expectancy (9.14 [standard deviation 0.12] versus 8.87 [standard deviation 0.13] quality-adjusted life years [QALYs]) compared to insulin glargine U100. IDegLira was associated with increased direct costs of $16,970, yielding an incremental cost-effectiveness ratio (ICER) of $63,678 per QALY gained versus insulin glargine U100. Sensitivity analyses identified that the key driver of cost-effectiveness was the greater reduction in glycated hemoglobin with IDegLira compared with insulin glargine U100. CONCLUSIONS: Based on head-to-head clinical trial data, the present analysis suggests that IDegLira is likely to improve long-term clinical outcomes for patients with T2DM not achieving glycemic control on basal insulin compared to re-education and up-titration of the dose of insulin glargine U100, with these improvements coming at an increased cost from a healthcare payer perspective. An ICER within the range described as high care value was calculated, suggesting IDegLira is a cost-effective treatment option in the US. Funding: Novo Nordisk A/S and Novo Nordisk Inc. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13300-017-0251-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5446378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-54463782017-06-12 IDegLira Versus Insulin Glargine U100: A Long-term Cost-effectiveness Analysis in the US Setting Hunt, Barnaby Mocarski, Michelle Valentine, William J. Langer, Jakob Diabetes Ther Original Research INTRODUCTION: Treatment with IDegLira has the potential to improve glycemic control in patients with type 2 diabetes mellitus (T2DM) without the weight gain and with a lower risk of hypoglycemia than with other therapies. The aim of the present analysis was to evaluate the long-term cost-effectiveness of IDegLira versus insulin glargine U100 with re-education and up-titration of the dose for treatment of patients with T2DM failing to achieve glycemic control on basal insulin in the US setting. METHODS: Data were obtained from the DUAL V randomized controlled trial in which adults with T2DM failing to achieve glycemic targets with insulin glargine U100 were randomly allocated to receive either IDegLira or insulin glargine U100. Long-term projections of clinical outcomes and direct costs were made using the IMS CORE Diabetes Model. Costs were accounted from a healthcare payer perspective. Future costs and clinical benefits were discounted at 3% annually. RESULTS: IDegLira was associated with improved discounted life expectancy (13.99 [standard deviation 0.19] versus 13.82 [standard deviation 0.20] years) and quality-adjusted life expectancy (9.14 [standard deviation 0.12] versus 8.87 [standard deviation 0.13] quality-adjusted life years [QALYs]) compared to insulin glargine U100. IDegLira was associated with increased direct costs of $16,970, yielding an incremental cost-effectiveness ratio (ICER) of $63,678 per QALY gained versus insulin glargine U100. Sensitivity analyses identified that the key driver of cost-effectiveness was the greater reduction in glycated hemoglobin with IDegLira compared with insulin glargine U100. CONCLUSIONS: Based on head-to-head clinical trial data, the present analysis suggests that IDegLira is likely to improve long-term clinical outcomes for patients with T2DM not achieving glycemic control on basal insulin compared to re-education and up-titration of the dose of insulin glargine U100, with these improvements coming at an increased cost from a healthcare payer perspective. An ICER within the range described as high care value was calculated, suggesting IDegLira is a cost-effective treatment option in the US. Funding: Novo Nordisk A/S and Novo Nordisk Inc. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13300-017-0251-x) contains supplementary material, which is available to authorized users. Springer Healthcare 2017-03-27 2017-06 /pmc/articles/PMC5446378/ /pubmed/28349444 http://dx.doi.org/10.1007/s13300-017-0251-x Text en © The Author(s) 2017 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Hunt, Barnaby Mocarski, Michelle Valentine, William J. Langer, Jakob IDegLira Versus Insulin Glargine U100: A Long-term Cost-effectiveness Analysis in the US Setting |
title | IDegLira Versus Insulin Glargine U100: A Long-term Cost-effectiveness Analysis in the US Setting |
title_full | IDegLira Versus Insulin Glargine U100: A Long-term Cost-effectiveness Analysis in the US Setting |
title_fullStr | IDegLira Versus Insulin Glargine U100: A Long-term Cost-effectiveness Analysis in the US Setting |
title_full_unstemmed | IDegLira Versus Insulin Glargine U100: A Long-term Cost-effectiveness Analysis in the US Setting |
title_short | IDegLira Versus Insulin Glargine U100: A Long-term Cost-effectiveness Analysis in the US Setting |
title_sort | ideglira versus insulin glargine u100: a long-term cost-effectiveness analysis in the us setting |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446378/ https://www.ncbi.nlm.nih.gov/pubmed/28349444 http://dx.doi.org/10.1007/s13300-017-0251-x |
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