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Once‐weekly semaglutide versus insulin aspart for the treatment of type 2 diabetes in the UK: A long‐term cost‐effectiveness analysis based on SUSTAIN 11

AIM: To evaluate the long‐term cost‐effectiveness of once‐weekly semaglutide 1 mg versus insulin aspart in the UK. MATERIALS AND METHODS: Long‐term outcomes were projected over patients' lifetimes using the IQVIA CORE Diabetes Model (vers 9.0). SUSTAIN 11 was used to inform baseline cohort char...

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Autores principales: Evans, Marc, Chubb, Barrie, Malkin, Samuel J. P., Berry, Sasha, Lawson, Jack, Hunt, Barnaby
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092031/
https://www.ncbi.nlm.nih.gov/pubmed/36251282
http://dx.doi.org/10.1111/dom.14892
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author Evans, Marc
Chubb, Barrie
Malkin, Samuel J. P.
Berry, Sasha
Lawson, Jack
Hunt, Barnaby
author_facet Evans, Marc
Chubb, Barrie
Malkin, Samuel J. P.
Berry, Sasha
Lawson, Jack
Hunt, Barnaby
author_sort Evans, Marc
collection PubMed
description AIM: To evaluate the long‐term cost‐effectiveness of once‐weekly semaglutide 1 mg versus insulin aspart in the UK. MATERIALS AND METHODS: Long‐term outcomes were projected over patients' lifetimes using the IQVIA CORE Diabetes Model (vers 9.0). SUSTAIN 11 was used to inform baseline cohort characteristics and treatment effects. Patients were modelled to receive once‐weekly semaglutide plus basal insulin for 3 years before intensifying to basal‐bolus insulin, compared with basal‐bolus insulin for lifetimes in the aspart arm. Costs were accounted from a healthcare payer perspective in the UK, expressed in 2021 pounds sterling (GBP). RESULTS: Once‐weekly semaglutide 1 mg was associated with improvements in quality‐adjusted life expectancy of 0.18 quality‐adjusted life years (QALYs) versus insulin aspart, due to a reduced incidence and delayed time to onset of diabetes‐related complications. Direct costs were estimated to be GBP 800 higher with semaglutide, with higher treatment costs partially offset by cost savings from avoidance of diabetes‐related complications. Once‐weekly semaglutide 1 mg was therefore associated with an incremental cost‐effectiveness ratio of GBP 4457 per QALY gained versus insulin aspart. CONCLUSIONS: Based on a willingness‐to‐pay threshold of GBP 20 000 per QALY gained, once‐weekly semaglutide 1 mg was projected to be highly cost‐effective versus insulin aspart for the treatment of type 2 diabetes in the UK.
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spelling pubmed-100920312023-04-13 Once‐weekly semaglutide versus insulin aspart for the treatment of type 2 diabetes in the UK: A long‐term cost‐effectiveness analysis based on SUSTAIN 11 Evans, Marc Chubb, Barrie Malkin, Samuel J. P. Berry, Sasha Lawson, Jack Hunt, Barnaby Diabetes Obes Metab Original Articles AIM: To evaluate the long‐term cost‐effectiveness of once‐weekly semaglutide 1 mg versus insulin aspart in the UK. MATERIALS AND METHODS: Long‐term outcomes were projected over patients' lifetimes using the IQVIA CORE Diabetes Model (vers 9.0). SUSTAIN 11 was used to inform baseline cohort characteristics and treatment effects. Patients were modelled to receive once‐weekly semaglutide plus basal insulin for 3 years before intensifying to basal‐bolus insulin, compared with basal‐bolus insulin for lifetimes in the aspart arm. Costs were accounted from a healthcare payer perspective in the UK, expressed in 2021 pounds sterling (GBP). RESULTS: Once‐weekly semaglutide 1 mg was associated with improvements in quality‐adjusted life expectancy of 0.18 quality‐adjusted life years (QALYs) versus insulin aspart, due to a reduced incidence and delayed time to onset of diabetes‐related complications. Direct costs were estimated to be GBP 800 higher with semaglutide, with higher treatment costs partially offset by cost savings from avoidance of diabetes‐related complications. Once‐weekly semaglutide 1 mg was therefore associated with an incremental cost‐effectiveness ratio of GBP 4457 per QALY gained versus insulin aspart. CONCLUSIONS: Based on a willingness‐to‐pay threshold of GBP 20 000 per QALY gained, once‐weekly semaglutide 1 mg was projected to be highly cost‐effective versus insulin aspart for the treatment of type 2 diabetes in the UK. Blackwell Publishing Ltd 2022-11-02 2023-02 /pmc/articles/PMC10092031/ /pubmed/36251282 http://dx.doi.org/10.1111/dom.14892 Text en © 2022 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Evans, Marc
Chubb, Barrie
Malkin, Samuel J. P.
Berry, Sasha
Lawson, Jack
Hunt, Barnaby
Once‐weekly semaglutide versus insulin aspart for the treatment of type 2 diabetes in the UK: A long‐term cost‐effectiveness analysis based on SUSTAIN 11
title Once‐weekly semaglutide versus insulin aspart for the treatment of type 2 diabetes in the UK: A long‐term cost‐effectiveness analysis based on SUSTAIN 11
title_full Once‐weekly semaglutide versus insulin aspart for the treatment of type 2 diabetes in the UK: A long‐term cost‐effectiveness analysis based on SUSTAIN 11
title_fullStr Once‐weekly semaglutide versus insulin aspart for the treatment of type 2 diabetes in the UK: A long‐term cost‐effectiveness analysis based on SUSTAIN 11
title_full_unstemmed Once‐weekly semaglutide versus insulin aspart for the treatment of type 2 diabetes in the UK: A long‐term cost‐effectiveness analysis based on SUSTAIN 11
title_short Once‐weekly semaglutide versus insulin aspart for the treatment of type 2 diabetes in the UK: A long‐term cost‐effectiveness analysis based on SUSTAIN 11
title_sort once‐weekly semaglutide versus insulin aspart for the treatment of type 2 diabetes in the uk: a long‐term cost‐effectiveness analysis based on sustain 11
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092031/
https://www.ncbi.nlm.nih.gov/pubmed/36251282
http://dx.doi.org/10.1111/dom.14892
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