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The potential population health impact of treating REDUCE-IT eligible US adults with Icosapent Ethyl
OBJECTIVE: To explore the population health impact of treating all US adults eligible for the Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial (REDUCE-IT) with icosapent ethyl (IPE), we estimated (1) the number of ASCVD events and healthcare costs that could be prevented; a...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097618/ https://www.ncbi.nlm.nih.gov/pubmed/35574517 http://dx.doi.org/10.1016/j.ajpc.2022.100345 |
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author | Derington, Catherine G. Bress, Adam P. Herrick, Jennifer S. Fan, Wenjun Wong, Nathan D. Andrade, Katherine E. Johnson, Jonathan Philip, Sephy Abrahamson, David Jiao, Lixia Bhatt, Deepak L. Weintraub, William S. |
author_facet | Derington, Catherine G. Bress, Adam P. Herrick, Jennifer S. Fan, Wenjun Wong, Nathan D. Andrade, Katherine E. Johnson, Jonathan Philip, Sephy Abrahamson, David Jiao, Lixia Bhatt, Deepak L. Weintraub, William S. |
author_sort | Derington, Catherine G. |
collection | PubMed |
description | OBJECTIVE: To explore the population health impact of treating all US adults eligible for the Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial (REDUCE-IT) with icosapent ethyl (IPE), we estimated (1) the number of ASCVD events and healthcare costs that could be prevented; and (2) medication costs. METHODS: We derived REDUCE-IT eligible cohorts in (1) the National Health and Nutrition Examination Surveys (NHANES) 2009-2014 and (2) the Optum Research Database (ORD). Population sizes were obtained from NHANES and observed first event rates (composite of cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, unstable angina requiring hospitalization, or coronary revascularization) were estimated from the ORD. Hazard ratios from REDUCE-IT USA estimated events prevented with IPE therapy. The National Inpatient Sample estimated event costs (facility and professional) and daily IPE treatment cost was approximated at $4.59. RESULTS: We estimate 3.6 million US adults to be REDUCE-IT eligible, and the observed five-year first event rate without IPE of 19.0% (95% confidence interval [CI] 16.6%-19.5%) could be lowered to 13.1% (95% CI 12.8%-13.5%) with five years of IPE treatment, preventing 212,000 (uncertainty range 163,000-262,000) events. We projected the annual IPE treatment cost for all eligible persons to be $6.0 billion (95% CI $4.7-$7.5 billion), but saving $1.8 billion annually due to first events prevented (net annual cost $4.3 billion). The total five-year event rate (first and recurrent) could be reduced from 42.5% (95% CI 39.6%-45.4%) to 28.9% (95% CI 26.9-30.9%) with five years of IPE therapy, preventing 490,000 (uncertainty range 370,000-609,000) events (net annual cost $2.6 billion). CONCLUSIONS: Treating all REDUCE-IT eligible US adults has substantial medication costs but could prevent a substantial number of ASCVD events and associated direct costs. Indirect cost savings by preventing events could outweigh much of the incurred direct costs. |
format | Online Article Text |
id | pubmed-9097618 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-90976182022-05-13 The potential population health impact of treating REDUCE-IT eligible US adults with Icosapent Ethyl Derington, Catherine G. Bress, Adam P. Herrick, Jennifer S. Fan, Wenjun Wong, Nathan D. Andrade, Katherine E. Johnson, Jonathan Philip, Sephy Abrahamson, David Jiao, Lixia Bhatt, Deepak L. Weintraub, William S. Am J Prev Cardiol Original Research Contribution OBJECTIVE: To explore the population health impact of treating all US adults eligible for the Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial (REDUCE-IT) with icosapent ethyl (IPE), we estimated (1) the number of ASCVD events and healthcare costs that could be prevented; and (2) medication costs. METHODS: We derived REDUCE-IT eligible cohorts in (1) the National Health and Nutrition Examination Surveys (NHANES) 2009-2014 and (2) the Optum Research Database (ORD). Population sizes were obtained from NHANES and observed first event rates (composite of cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, unstable angina requiring hospitalization, or coronary revascularization) were estimated from the ORD. Hazard ratios from REDUCE-IT USA estimated events prevented with IPE therapy. The National Inpatient Sample estimated event costs (facility and professional) and daily IPE treatment cost was approximated at $4.59. RESULTS: We estimate 3.6 million US adults to be REDUCE-IT eligible, and the observed five-year first event rate without IPE of 19.0% (95% confidence interval [CI] 16.6%-19.5%) could be lowered to 13.1% (95% CI 12.8%-13.5%) with five years of IPE treatment, preventing 212,000 (uncertainty range 163,000-262,000) events. We projected the annual IPE treatment cost for all eligible persons to be $6.0 billion (95% CI $4.7-$7.5 billion), but saving $1.8 billion annually due to first events prevented (net annual cost $4.3 billion). The total five-year event rate (first and recurrent) could be reduced from 42.5% (95% CI 39.6%-45.4%) to 28.9% (95% CI 26.9-30.9%) with five years of IPE therapy, preventing 490,000 (uncertainty range 370,000-609,000) events (net annual cost $2.6 billion). CONCLUSIONS: Treating all REDUCE-IT eligible US adults has substantial medication costs but could prevent a substantial number of ASCVD events and associated direct costs. Indirect cost savings by preventing events could outweigh much of the incurred direct costs. Elsevier 2022-04-28 /pmc/articles/PMC9097618/ /pubmed/35574517 http://dx.doi.org/10.1016/j.ajpc.2022.100345 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Contribution Derington, Catherine G. Bress, Adam P. Herrick, Jennifer S. Fan, Wenjun Wong, Nathan D. Andrade, Katherine E. Johnson, Jonathan Philip, Sephy Abrahamson, David Jiao, Lixia Bhatt, Deepak L. Weintraub, William S. The potential population health impact of treating REDUCE-IT eligible US adults with Icosapent Ethyl |
title | The potential population health impact of treating REDUCE-IT eligible US adults with Icosapent Ethyl |
title_full | The potential population health impact of treating REDUCE-IT eligible US adults with Icosapent Ethyl |
title_fullStr | The potential population health impact of treating REDUCE-IT eligible US adults with Icosapent Ethyl |
title_full_unstemmed | The potential population health impact of treating REDUCE-IT eligible US adults with Icosapent Ethyl |
title_short | The potential population health impact of treating REDUCE-IT eligible US adults with Icosapent Ethyl |
title_sort | potential population health impact of treating reduce-it eligible us adults with icosapent ethyl |
topic | Original Research Contribution |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9097618/ https://www.ncbi.nlm.nih.gov/pubmed/35574517 http://dx.doi.org/10.1016/j.ajpc.2022.100345 |
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