TY - JOUR
T1 - Effect of ticagrelor on the outcomes of patients with prior coronary artery bypass graft surgery
T2 - Insights from the PLATelet inhibition and patient outcomes (PLATO) trial
AU - Brilakis, Emmanouil S.
AU - Held, Claes
AU - Meier, Bernhard
AU - Cools, Frank
AU - Claeys, Marc J.
AU - Cornel, Jan H.
AU - Aylward, Philip
AU - Lewis, Basil S.
AU - Weaver, Douglas
AU - Brandrup-Wognsen, Gunnar
AU - Stevens, Susanna R.
AU - Himmelmann, Anders
AU - Wallentin, Lars
AU - James, Stefan K.
N1 - Funding Information:
E. S. Brilakis: speaker honoraria from St Jude Medical, Terumo, and Bridgepoint Medical; research support from Guerbet; spouse is an employee of Medtronic. C. Held: institutional research grants from AstraZeneca, Merck, GlaxoSmithKline, Roche, and Bristol-Myers Squibb and being an advisory board member for AstraZeneca; honoraria from AstraZeneca. B. Meier: consultant/advisory board; AstraZeneca, Bayer, Boehringer-Ingelheim, Daiichi Sankyo, Eli Lilly, and Sanofi Aventis. F. Cools: reports speaker's fees from Astra Zeneca and Bayer; consultancy fees from Novartis. M. J. Claeys: honoraria from AstraZeneca and Eli Lilly, consultant/advisory board fees from AstraZeneca and Eli Lilly. J. H. Cornel: advisory board fees from BMS, AstraZeneca, Eli Lilly/Daiichi Sankyo; consultancy fees from Merck and Servier. P. Aylward: research support from AstraZeneca, Merck & Co, Eli Lilly, Bayer/Johnson & Johnson, Sanofi Aventis, GlaxoSmithKline, and Daiichi Sankyo; consultant and advisory board fees from Boeringer Ingelheim, AstraZeneca, Pfizer, Sanofi Aventis, and Eli Lilly; and travel support from Bristol Myers Squibb, AstraZeneca, and Boeringer Ingelheim. B. S. Lewis: consultant/advisory board Bayer Healthcare, Merck, and Bristol-Myers Squibb/Pfizer and research grants from AstraZeneca, Daiichi Sankyo, Eli Lilly, Merck/Schering-Plough, Boehringer-Ingelheim, and Bristol-Myers Squibb/Pfizer. D. W. Weaver: none. G. Brandrup-Wognsen: employee of AstraZeneca; equity ownership in AstraZeneca. S. R. Stevens: none. A. Himmelmann: reports being an employee of AstraZeneca. L. Wallentin: research grants from AstraZeneca, Merck & Co, Boehringer-Ingelheim, Bristol-Myers Squibb/Pfizer, and GlaxoSmithKline; consultant for Merck & Co, Regado Biosciences, Evolva, Portola, C.S.L. Behring, Athera Biotechnologies, Boehringer-Ingelheim, AstraZeneca, GlaxoSmithKline, and Bristol-Myers Squibb/Pfizer; lecture fees from AstraZeneca, Boehringer-Ingelheim, Bristol-Myers Squibb/Pfizer, GlaxoSmithKline, and Merck & Co; honoraria from Boehringer Ingelheim, AstraZeneca, Bristol-Myers Squibb/Pfizer, GlaxoSmithKline, and Merck & Co; travel support from Bristol-Myers Squibb/Pfizer. S. K. James: institutional research grant and honoraria from AstraZeneca, Eli Lilly, Merck, and Bristol-Myers Squibb; advisory board member for AstraZeneca, Eli Lilly, and Merck; honoraria from The Medicines Company.
PY - 2013/9
Y1 - 2013/9
N2 - Background Patients with prior coronary artery bypass graft surgery (CABG) who present with an acute coronary syndrome have a high risk for recurrent events. Whether intensive antiplatelet therapy with ticagrelor might be beneficial compared with clopidogrel is unknown. In this substudy of the PLATO trial, we studied the effects of randomized treatment dependent on history of CABG. Methods Patients participating in PLATO were classified according to whether they had undergone prior CABG. The trial's primary and secondary end points were compared using Cox proportional hazards regression. Results Of the 18,613 study patients, 1,133 (6.1%) had prior CABG. Prior-CABG patients had more high-risk characteristics at study entry and a 2-fold increase in clinical events during follow-up, but less major bleeding. The primary end point (composite of cardiovascular death, myocardial infarction, and stroke) was reduced to a similar extent by ticagrelor among patients with (19.6% vs 21.4%; adjusted hazard ratio [HR], 0.91 [0.67, 1.24]) and without (9.2% vs 11.0%; adjusted HR, 0.86 [0.77, 0.96]; Pinteraction =.73) prior CABG. Major bleeding was similar with ticagrelor versus clopidogrel among patients with (8.1% vs 8.7%; adjusted HR, 0.89 [0.55, 1.47]) and without (11.8% vs 11.4%; HR, 1.08 [0.98, 1.20]; Pinteraction =.46) prior CABG. Conclusions Prior-CABG patients presenting with acute coronary syndrome are a high-risk cohort for death and recurrent cardiovascular events but have a lower risk for major bleeding. Similar to the results in no-prior-CABG patients, ticagrelor was associated with a reduction in ischemic events without an increase in major bleeding.
AB - Background Patients with prior coronary artery bypass graft surgery (CABG) who present with an acute coronary syndrome have a high risk for recurrent events. Whether intensive antiplatelet therapy with ticagrelor might be beneficial compared with clopidogrel is unknown. In this substudy of the PLATO trial, we studied the effects of randomized treatment dependent on history of CABG. Methods Patients participating in PLATO were classified according to whether they had undergone prior CABG. The trial's primary and secondary end points were compared using Cox proportional hazards regression. Results Of the 18,613 study patients, 1,133 (6.1%) had prior CABG. Prior-CABG patients had more high-risk characteristics at study entry and a 2-fold increase in clinical events during follow-up, but less major bleeding. The primary end point (composite of cardiovascular death, myocardial infarction, and stroke) was reduced to a similar extent by ticagrelor among patients with (19.6% vs 21.4%; adjusted hazard ratio [HR], 0.91 [0.67, 1.24]) and without (9.2% vs 11.0%; adjusted HR, 0.86 [0.77, 0.96]; Pinteraction =.73) prior CABG. Major bleeding was similar with ticagrelor versus clopidogrel among patients with (8.1% vs 8.7%; adjusted HR, 0.89 [0.55, 1.47]) and without (11.8% vs 11.4%; HR, 1.08 [0.98, 1.20]; Pinteraction =.46) prior CABG. Conclusions Prior-CABG patients presenting with acute coronary syndrome are a high-risk cohort for death and recurrent cardiovascular events but have a lower risk for major bleeding. Similar to the results in no-prior-CABG patients, ticagrelor was associated with a reduction in ischemic events without an increase in major bleeding.
UR - http://www.scopus.com/inward/record.url?scp=84883807129&partnerID=8YFLogxK
U2 - 10.1016/j.ahj.2013.06.019
DO - 10.1016/j.ahj.2013.06.019
M3 - Article
C2 - 24016496
AN - SCOPUS:84883807129
SN - 0002-8703
VL - 166
SP - 474
EP - 480
JO - American Heart Journal
JF - American Heart Journal
IS - 3
ER -