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Cost-Effectiveness of Lipid-Lowering Therapies for Cardiovascular Prevention in Germany

PURPOSE: Novel pharmaceutical treatments reducing cardiovascular events in dyslipidaemia patients must demonstrate clinical efficacy and cost-effectiveness to promote long-term adoption by patients, physicians, and insurers. OBJECTIVE: To assess the cost-effectiveness of statin monotherapy compared...

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Autores principales: Michaeli, Daniel Tobias, Michaeli, Julia Caroline, Boch, Tobias, Michaeli, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397126/
https://www.ncbi.nlm.nih.gov/pubmed/35015186
http://dx.doi.org/10.1007/s10557-021-07310-y
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author Michaeli, Daniel Tobias
Michaeli, Julia Caroline
Boch, Tobias
Michaeli, Thomas
author_facet Michaeli, Daniel Tobias
Michaeli, Julia Caroline
Boch, Tobias
Michaeli, Thomas
author_sort Michaeli, Daniel Tobias
collection PubMed
description PURPOSE: Novel pharmaceutical treatments reducing cardiovascular events in dyslipidaemia patients must demonstrate clinical efficacy and cost-effectiveness to promote long-term adoption by patients, physicians, and insurers. OBJECTIVE: To assess the cost-effectiveness of statin monotherapy compared to additive lipid-lowering therapies for primary and secondary cardiovascular prevention from the perspective of Germany’s healthcare system. METHODS: Transition probabilities and hazard ratios were derived from cardiovascular outcome trials for statin combinations with icosapent ethyl (REDUCE-IT), evolocumab (FOURIER), alirocumab (ODYSSEY), ezetimibe (IMPROVE-IT), and fibrate (ACCORD). Costs and utilities were retrieved from previous literature. The incidence of major adverse cardiovascular events was simulated with a Markov cohort model. The main outcomes were the incremental cost-effectiveness ratios (ICER) per quality adjusted life year (QALY) gained. RESULTS: For primary prevention, the addition of icosapent ethyl to statin generated 0.81 QALY and €14,732 costs (ICER: 18,133), whereas fibrates yielded 0.63 QALY and € − 10,516 costs (ICER: − 16,632). For secondary prevention, the addition of ezetimibe to statin provided 0.61 QALY at savings of € − 5,796 (ICER: − 9,555) and icosapent ethyl yielded 0.99 QALY and €14,333 costs (ICER: 14,485). PCSK9 inhibitors offered 0.55 and 0.87 QALY at costs of €62,722 and €87,002 for evolocumab (ICER: 114,639) and alirocumab (ICER: 100,532), respectively. A 95% probability of cost-effectiveness was surpassed at €20,000 for icosapent ethyl (primary and secondary prevention), €119,000 for alirocumab, and €149,000 for evolocumab. CONCLUSIONS: For primary cardiovascular prevention, a combination therapy of icosapent ethyl plus statin is a cost-effective use of resources compared to statin monotherapy. For secondary prevention, icosapent ethyl, ezetimibe, evolocumab, and alirocumab increase patient benefit at different economic costs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10557-021-07310-y.
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spelling pubmed-103971262023-08-04 Cost-Effectiveness of Lipid-Lowering Therapies for Cardiovascular Prevention in Germany Michaeli, Daniel Tobias Michaeli, Julia Caroline Boch, Tobias Michaeli, Thomas Cardiovasc Drugs Ther Original Article PURPOSE: Novel pharmaceutical treatments reducing cardiovascular events in dyslipidaemia patients must demonstrate clinical efficacy and cost-effectiveness to promote long-term adoption by patients, physicians, and insurers. OBJECTIVE: To assess the cost-effectiveness of statin monotherapy compared to additive lipid-lowering therapies for primary and secondary cardiovascular prevention from the perspective of Germany’s healthcare system. METHODS: Transition probabilities and hazard ratios were derived from cardiovascular outcome trials for statin combinations with icosapent ethyl (REDUCE-IT), evolocumab (FOURIER), alirocumab (ODYSSEY), ezetimibe (IMPROVE-IT), and fibrate (ACCORD). Costs and utilities were retrieved from previous literature. The incidence of major adverse cardiovascular events was simulated with a Markov cohort model. The main outcomes were the incremental cost-effectiveness ratios (ICER) per quality adjusted life year (QALY) gained. RESULTS: For primary prevention, the addition of icosapent ethyl to statin generated 0.81 QALY and €14,732 costs (ICER: 18,133), whereas fibrates yielded 0.63 QALY and € − 10,516 costs (ICER: − 16,632). For secondary prevention, the addition of ezetimibe to statin provided 0.61 QALY at savings of € − 5,796 (ICER: − 9,555) and icosapent ethyl yielded 0.99 QALY and €14,333 costs (ICER: 14,485). PCSK9 inhibitors offered 0.55 and 0.87 QALY at costs of €62,722 and €87,002 for evolocumab (ICER: 114,639) and alirocumab (ICER: 100,532), respectively. A 95% probability of cost-effectiveness was surpassed at €20,000 for icosapent ethyl (primary and secondary prevention), €119,000 for alirocumab, and €149,000 for evolocumab. CONCLUSIONS: For primary cardiovascular prevention, a combination therapy of icosapent ethyl plus statin is a cost-effective use of resources compared to statin monotherapy. For secondary prevention, icosapent ethyl, ezetimibe, evolocumab, and alirocumab increase patient benefit at different economic costs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10557-021-07310-y. Springer US 2022-01-11 2023 /pmc/articles/PMC10397126/ /pubmed/35015186 http://dx.doi.org/10.1007/s10557-021-07310-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Michaeli, Daniel Tobias
Michaeli, Julia Caroline
Boch, Tobias
Michaeli, Thomas
Cost-Effectiveness of Lipid-Lowering Therapies for Cardiovascular Prevention in Germany
title Cost-Effectiveness of Lipid-Lowering Therapies for Cardiovascular Prevention in Germany
title_full Cost-Effectiveness of Lipid-Lowering Therapies for Cardiovascular Prevention in Germany
title_fullStr Cost-Effectiveness of Lipid-Lowering Therapies for Cardiovascular Prevention in Germany
title_full_unstemmed Cost-Effectiveness of Lipid-Lowering Therapies for Cardiovascular Prevention in Germany
title_short Cost-Effectiveness of Lipid-Lowering Therapies for Cardiovascular Prevention in Germany
title_sort cost-effectiveness of lipid-lowering therapies for cardiovascular prevention in germany
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397126/
https://www.ncbi.nlm.nih.gov/pubmed/35015186
http://dx.doi.org/10.1007/s10557-021-07310-y
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