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β-blockers, calcium antagonists, and mortality in stable coronary artery disease: an international cohort study

AIMS: The effect of first-line antianginal agents, β-blockers, and calcium antagonists on clinical outcomes in stable coronary artery disease (CAD) remains uncertain. METHODS AND RESULTS: We analysed the use of β-blockers or calcium antagonists (baseline and annually) and outcomes in 22 006 stable C...

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Autores principales: Sorbets, Emmanuel, Steg, Philippe Gabriel, Young, Robin, Danchin, Nicolas, Greenlaw, Nicola, Ford, Ian, Tendera, Michal, Ferrari, Roberto, Merkely, Bela, Parkhomenko, Alexander, Reid, Christopher, Tardif, Jean-Claude, Fox, Kim M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503455/
https://www.ncbi.nlm.nih.gov/pubmed/30590529
http://dx.doi.org/10.1093/eurheartj/ehy811
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author Sorbets, Emmanuel
Steg, Philippe Gabriel
Young, Robin
Danchin, Nicolas
Greenlaw, Nicola
Ford, Ian
Tendera, Michal
Ferrari, Roberto
Merkely, Bela
Parkhomenko, Alexander
Reid, Christopher
Tardif, Jean-Claude
Fox, Kim M
author_facet Sorbets, Emmanuel
Steg, Philippe Gabriel
Young, Robin
Danchin, Nicolas
Greenlaw, Nicola
Ford, Ian
Tendera, Michal
Ferrari, Roberto
Merkely, Bela
Parkhomenko, Alexander
Reid, Christopher
Tardif, Jean-Claude
Fox, Kim M
author_sort Sorbets, Emmanuel
collection PubMed
description AIMS: The effect of first-line antianginal agents, β-blockers, and calcium antagonists on clinical outcomes in stable coronary artery disease (CAD) remains uncertain. METHODS AND RESULTS: We analysed the use of β-blockers or calcium antagonists (baseline and annually) and outcomes in 22 006 stable CAD patients (enrolled 2009–2010) followed annually to 5 years, in the CLARIFY registry (45 countries). Primary outcome was all-cause death. Secondary outcomes were cardiovascular death and the composite of cardiovascular death/non-fatal myocardial infarction (MI). After multivariable adjustment, baseline β-blocker use was not associated with lower all-cause death [1345 (7.8%) in users vs. 407 (8.4%) in non-users; hazard ratio (HR) 0.94, 95% confidence interval (CI) 0.84–1.06; P = 0.30]; cardiovascular death [861 (5.0%) vs. 262 (5.4%); HR 0.91, 95% CI 0.79–1.05; P = 0.20]; or cardiovascular death/non-fatal MI [1272 (7.4%) vs. 340 (7.0%); HR 1.03, 95% CI 0.91–1.16; P = 0.66]. Sensitivity analyses according to β-blocker use over time and to prescribed dose produced similar results. Among prior MI patients, for those enrolled in the year following MI, baseline β-blocker use was associated with lower all-cause death [205 (7.0%) vs. 59 (10.3%); HR 0.68, 95% CI 0.50–0.91; P = 0.01]; cardiovascular death [132 (4.5%) vs. 49 (8.5%); HR 0.52, 95% CI 0.37–0.73; P = 0.0001]; and cardiovascular death/non-fatal MI [212 (7.2%) vs. 59 (10.3%); HR 0.69, 95% CI 0.52–0.93; P = 0.01]. Calcium antagonists were not associated with any difference in mortality. CONCLUSION: In this contemporary cohort of stable CAD, β-blocker use was associated with lower 5-year mortality only in patients enrolled in the year following MI. Use of calcium antagonists was not associated with superior mortality, regardless of history of MI.
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spelling pubmed-65034552019-05-09 β-blockers, calcium antagonists, and mortality in stable coronary artery disease: an international cohort study Sorbets, Emmanuel Steg, Philippe Gabriel Young, Robin Danchin, Nicolas Greenlaw, Nicola Ford, Ian Tendera, Michal Ferrari, Roberto Merkely, Bela Parkhomenko, Alexander Reid, Christopher Tardif, Jean-Claude Fox, Kim M Eur Heart J Fast Track Clinical Research AIMS: The effect of first-line antianginal agents, β-blockers, and calcium antagonists on clinical outcomes in stable coronary artery disease (CAD) remains uncertain. METHODS AND RESULTS: We analysed the use of β-blockers or calcium antagonists (baseline and annually) and outcomes in 22 006 stable CAD patients (enrolled 2009–2010) followed annually to 5 years, in the CLARIFY registry (45 countries). Primary outcome was all-cause death. Secondary outcomes were cardiovascular death and the composite of cardiovascular death/non-fatal myocardial infarction (MI). After multivariable adjustment, baseline β-blocker use was not associated with lower all-cause death [1345 (7.8%) in users vs. 407 (8.4%) in non-users; hazard ratio (HR) 0.94, 95% confidence interval (CI) 0.84–1.06; P = 0.30]; cardiovascular death [861 (5.0%) vs. 262 (5.4%); HR 0.91, 95% CI 0.79–1.05; P = 0.20]; or cardiovascular death/non-fatal MI [1272 (7.4%) vs. 340 (7.0%); HR 1.03, 95% CI 0.91–1.16; P = 0.66]. Sensitivity analyses according to β-blocker use over time and to prescribed dose produced similar results. Among prior MI patients, for those enrolled in the year following MI, baseline β-blocker use was associated with lower all-cause death [205 (7.0%) vs. 59 (10.3%); HR 0.68, 95% CI 0.50–0.91; P = 0.01]; cardiovascular death [132 (4.5%) vs. 49 (8.5%); HR 0.52, 95% CI 0.37–0.73; P = 0.0001]; and cardiovascular death/non-fatal MI [212 (7.2%) vs. 59 (10.3%); HR 0.69, 95% CI 0.52–0.93; P = 0.01]. Calcium antagonists were not associated with any difference in mortality. CONCLUSION: In this contemporary cohort of stable CAD, β-blocker use was associated with lower 5-year mortality only in patients enrolled in the year following MI. Use of calcium antagonists was not associated with superior mortality, regardless of history of MI. Oxford University Press 2019-05-07 2019-05-07 /pmc/articles/PMC6503455/ /pubmed/30590529 http://dx.doi.org/10.1093/eurheartj/ehy811 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the European Society of Cardiology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Fast Track Clinical Research
Sorbets, Emmanuel
Steg, Philippe Gabriel
Young, Robin
Danchin, Nicolas
Greenlaw, Nicola
Ford, Ian
Tendera, Michal
Ferrari, Roberto
Merkely, Bela
Parkhomenko, Alexander
Reid, Christopher
Tardif, Jean-Claude
Fox, Kim M
β-blockers, calcium antagonists, and mortality in stable coronary artery disease: an international cohort study
title β-blockers, calcium antagonists, and mortality in stable coronary artery disease: an international cohort study
title_full β-blockers, calcium antagonists, and mortality in stable coronary artery disease: an international cohort study
title_fullStr β-blockers, calcium antagonists, and mortality in stable coronary artery disease: an international cohort study
title_full_unstemmed β-blockers, calcium antagonists, and mortality in stable coronary artery disease: an international cohort study
title_short β-blockers, calcium antagonists, and mortality in stable coronary artery disease: an international cohort study
title_sort β-blockers, calcium antagonists, and mortality in stable coronary artery disease: an international cohort study
topic Fast Track Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6503455/
https://www.ncbi.nlm.nih.gov/pubmed/30590529
http://dx.doi.org/10.1093/eurheartj/ehy811
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