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dc.contributor.authorSorbets, E.
dc.contributor.authorSteg, P.G.
dc.contributor.authorYoung, R.
dc.contributor.authorDanchin, N.
dc.contributor.authorGreenlaw, N.
dc.contributor.authorFord, I.
dc.contributor.authorTendera, M.
dc.contributor.authorFerrari, R.
dc.contributor.authorMerkely, B.
dc.contributor.authorParkhomenko, A.
dc.contributor.authorReid, Christopher
dc.contributor.authorTardif, J.C.
dc.contributor.authorFox, K.M.
dc.date.accessioned2020-07-16T03:58:43Z
dc.date.available2020-07-16T03:58:43Z
dc.date.issued2019
dc.identifier.citationSorbets, E. and Steg, P.G. and Young, R. and Danchin, N. and Greenlaw, N. and Ford, I. and Tendera, M. et al. 2019. B-blockers, calcium antagonists, and mortality in stable coronary artery disease: An international cohort study. European Heart Journal. 40 (18): pp. 1399-1407.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/80057
dc.identifier.doi10.1093/eurheartj/ehy811
dc.description.abstract

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.

dc.languageeng
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectBeta-blockers
dc.subjectCalcium antagonists
dc.subjectMortality
dc.subjectPrognosis
dc.subjectStable coronary artery disease
dc.titleB-blockers, calcium antagonists, and mortality in stable coronary artery disease: An international cohort study
dc.typeJournal Article
dcterms.source.volume40
dcterms.source.number18
dcterms.source.startPage1399
dcterms.source.endPage1407
dcterms.source.issn0195-668X
dcterms.source.titleEuropean Heart Journal
dc.date.updated2020-07-16T03:58:41Z
curtin.note

© The Author(s) 2018. Published by Oxford University Press on behalf of the European Society of Cardiology.

curtin.departmentSchool of Public Health
curtin.accessStatusOpen access
curtin.facultyFaculty of Health Sciences
curtin.contributor.orcidReid, Christopher [0000-0001-9173-3944]
dcterms.source.eissn1522-9645


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