Cargando…

Applicability of the REDUCE‐IT trial to the FAST‐MI registry. Are the results of randomized trials relevant in routine clinical practice?

BACKGROUND: The reduction of cardiovascular events with icosapent ethyl‐intervention trial (REDUCE‐IT) trial revealed robust atherosclerotic cardiovascular risk reduction with a strategy comprising high‐dose omega‐3 icosapent ethyl vs placebo in statin‐treated patients with elevated triglycerides an...

Descripción completa

Detalles Bibliográficos
Autores principales: Ferrières, Jean, Bataille, Vincent, Puymirat, Etienne, Schiele, François, Simon, Tabassome, Danchin, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7661650/
https://www.ncbi.nlm.nih.gov/pubmed/32720384
http://dx.doi.org/10.1002/clc.23437
_version_ 1783609241895960576
author Ferrières, Jean
Bataille, Vincent
Puymirat, Etienne
Schiele, François
Simon, Tabassome
Danchin, Nicolas
author_facet Ferrières, Jean
Bataille, Vincent
Puymirat, Etienne
Schiele, François
Simon, Tabassome
Danchin, Nicolas
author_sort Ferrières, Jean
collection PubMed
description BACKGROUND: The reduction of cardiovascular events with icosapent ethyl‐intervention trial (REDUCE‐IT) trial revealed robust atherosclerotic cardiovascular risk reduction with a strategy comprising high‐dose omega‐3 icosapent ethyl vs placebo in statin‐treated patients with elevated triglycerides and controlled low‐density lipoprotein cholesterol (LDL‐C). HYPOTHESIS: Are the results of the REDUCE‐IT trial applicable to the French registry on acute ST‐elevation and non‐ST‐elevation myocardial infarction (FAST‐MI) population? METHODS: Data were extracted from the FAST‐MI 2010 and 2015 registries. We applied the REDUCE‐IT enrolment criteria (triglycerides 150‐500 mg/dL and LDL‐C 40‐100 mg/dL on statins) to the FAST‐MI population in patients aged ≥45 years who had detailed lipid values postacute hospitalization, focusing on their clinical profile and cardiovascular prognosis. RESULTS: Of the 3789 FAST‐MI patients with a full lipid profile (median 11.1 [IQR 7.6‐17.4] months after hospitalization for myocardial infarction), 472 (12.5%; 95% CI 11.4‐13.5) met the eligibility criteria for REDUCE‐IT (REDUCE‐IT‐like group). The cardiovascular event rate (all‐cause death, nonfatal myocardial infarction, nonfatal stroke) was 36.7 (95% CI 27.8‐48.6) per 1000 person‐years for the REDUCE‐IT‐like group, which compares with the 36.9 (95% CI 26.1‐51.5) per 1000 person‐years (cardiovascular death, nonfatal myocardial infarction, nonfatal stroke) reported in the REDUCE‐IT trial. The residual cardiovascular risk related to elevated triglycerides in the REDUCE‐IT‐like group was similar to the risk in the REDUCE‐IT trial. CONCLUSIONS: If the results of REDUCE‐IT are applied to patients hospitalized for a myocardial infarction in France, 12.5% of these patients could benefit from a strategy of high‐dose omega‐3 icosapent ethyl on top of contemporary therapy including statins to improve their clinical outcomes.
format Online
Article
Text
id pubmed-7661650
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Wiley Periodicals, Inc.
record_format MEDLINE/PubMed
spelling pubmed-76616502020-11-17 Applicability of the REDUCE‐IT trial to the FAST‐MI registry. Are the results of randomized trials relevant in routine clinical practice? Ferrières, Jean Bataille, Vincent Puymirat, Etienne Schiele, François Simon, Tabassome Danchin, Nicolas Clin Cardiol Clinical Investigations BACKGROUND: The reduction of cardiovascular events with icosapent ethyl‐intervention trial (REDUCE‐IT) trial revealed robust atherosclerotic cardiovascular risk reduction with a strategy comprising high‐dose omega‐3 icosapent ethyl vs placebo in statin‐treated patients with elevated triglycerides and controlled low‐density lipoprotein cholesterol (LDL‐C). HYPOTHESIS: Are the results of the REDUCE‐IT trial applicable to the French registry on acute ST‐elevation and non‐ST‐elevation myocardial infarction (FAST‐MI) population? METHODS: Data were extracted from the FAST‐MI 2010 and 2015 registries. We applied the REDUCE‐IT enrolment criteria (triglycerides 150‐500 mg/dL and LDL‐C 40‐100 mg/dL on statins) to the FAST‐MI population in patients aged ≥45 years who had detailed lipid values postacute hospitalization, focusing on their clinical profile and cardiovascular prognosis. RESULTS: Of the 3789 FAST‐MI patients with a full lipid profile (median 11.1 [IQR 7.6‐17.4] months after hospitalization for myocardial infarction), 472 (12.5%; 95% CI 11.4‐13.5) met the eligibility criteria for REDUCE‐IT (REDUCE‐IT‐like group). The cardiovascular event rate (all‐cause death, nonfatal myocardial infarction, nonfatal stroke) was 36.7 (95% CI 27.8‐48.6) per 1000 person‐years for the REDUCE‐IT‐like group, which compares with the 36.9 (95% CI 26.1‐51.5) per 1000 person‐years (cardiovascular death, nonfatal myocardial infarction, nonfatal stroke) reported in the REDUCE‐IT trial. The residual cardiovascular risk related to elevated triglycerides in the REDUCE‐IT‐like group was similar to the risk in the REDUCE‐IT trial. CONCLUSIONS: If the results of REDUCE‐IT are applied to patients hospitalized for a myocardial infarction in France, 12.5% of these patients could benefit from a strategy of high‐dose omega‐3 icosapent ethyl on top of contemporary therapy including statins to improve their clinical outcomes. Wiley Periodicals, Inc. 2020-07-28 /pmc/articles/PMC7661650/ /pubmed/32720384 http://dx.doi.org/10.1002/clc.23437 Text en © 2020 The Authors. Clinical Cardiology published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigations
Ferrières, Jean
Bataille, Vincent
Puymirat, Etienne
Schiele, François
Simon, Tabassome
Danchin, Nicolas
Applicability of the REDUCE‐IT trial to the FAST‐MI registry. Are the results of randomized trials relevant in routine clinical practice?
title Applicability of the REDUCE‐IT trial to the FAST‐MI registry. Are the results of randomized trials relevant in routine clinical practice?
title_full Applicability of the REDUCE‐IT trial to the FAST‐MI registry. Are the results of randomized trials relevant in routine clinical practice?
title_fullStr Applicability of the REDUCE‐IT trial to the FAST‐MI registry. Are the results of randomized trials relevant in routine clinical practice?
title_full_unstemmed Applicability of the REDUCE‐IT trial to the FAST‐MI registry. Are the results of randomized trials relevant in routine clinical practice?
title_short Applicability of the REDUCE‐IT trial to the FAST‐MI registry. Are the results of randomized trials relevant in routine clinical practice?
title_sort applicability of the reduce‐it trial to the fast‐mi registry. are the results of randomized trials relevant in routine clinical practice?
topic Clinical Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7661650/
https://www.ncbi.nlm.nih.gov/pubmed/32720384
http://dx.doi.org/10.1002/clc.23437
work_keys_str_mv AT ferrieresjean applicabilityofthereduceittrialtothefastmiregistryaretheresultsofrandomizedtrialsrelevantinroutineclinicalpractice
AT bataillevincent applicabilityofthereduceittrialtothefastmiregistryaretheresultsofrandomizedtrialsrelevantinroutineclinicalpractice
AT puymiratetienne applicabilityofthereduceittrialtothefastmiregistryaretheresultsofrandomizedtrialsrelevantinroutineclinicalpractice
AT schielefrancois applicabilityofthereduceittrialtothefastmiregistryaretheresultsofrandomizedtrialsrelevantinroutineclinicalpractice
AT simontabassome applicabilityofthereduceittrialtothefastmiregistryaretheresultsofrandomizedtrialsrelevantinroutineclinicalpractice
AT danchinnicolas applicabilityofthereduceittrialtothefastmiregistryaretheresultsofrandomizedtrialsrelevantinroutineclinicalpractice
AT applicabilityofthereduceittrialtothefastmiregistryaretheresultsofrandomizedtrialsrelevantinroutineclinicalpractice