TY - JOUR
T1 - Oral anticoagulation and antiplatelets in atrial fibrillation patients after myocardial infarction and coronary intervention
AU - Lamberts, Morten
AU - Gislason, Gunnar H
AU - Olesen, Jonas Bjerring
AU - Kristensen, Søren Lund
AU - Schjerning Olsen, Anne-Marie
AU - Mikkelsen, Anders
AU - Christensen, Christine Benn
AU - Lip, Gregory Y.H.
AU - Køber, Lars
AU - Torp-Pedersen, Christian
AU - Hansen, Morten Lock
N1 - Copyright © 2013 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
PY - 2013/9
Y1 - 2013/9
N2 - OBJECTIVES: To investigate the risk of thrombosis and bleeding according to multiple antithrombotic treatment regimens in atrial fibrillation (AF) patients after myocardial infarction (MI) or percutaneous coronary intervention (PCI) BACKGROUND: The optimal antithrombotic treatment strategy is unresolved in patients with multiple indications. METHODS: A total of 12,165 AF patients hospitalized with MI and/or undergoing PCI between 2001-2009 were identified by nationwide registries (60.7% males, mean age 75.6 years). Risk of MI/coronary death, ischemic stroke, and bleeding according to antithrombotic treatment regimen was estimated by Cox regression models. RESULTS: Within one year, MI or coronary death, ischemic stroke, and bleeding events occurred in 2,255 (18.5%), 680 (5.6%), and 769 (6.3%) patients, respectively. Relative to triple therapy (oral anticoagulation (OAC) + aspirin + clopidogrel), no increased risk of recurrent coronary events was seen for OAC + clopidogrel (hazard ratio [HR] 0.69 [0.48-1.00]), OAC + aspirin (HR 0.96 [0.77-1.19]), or aspirin + clopidogrel (HR 1.17 [0.96-1.42]), but aspirin + clopidogrel resulted in a higher risk of ischemic stroke (HR 1.50 [1.03-2.20]). Also, OAC + aspirin and aspirin + clopidogrel were associated with a significant increased risk of all-cause death (HR 1.52 [1.17-1.99] and 1.60 [1.25-2.05]). When compared to triple therapy, bleeding risk was non-significantly reduced for OAC + clopidogrel (HR 0.78 [0.55-1.12]) and significantly reduced for OAC + aspirin and aspirin + clopidogrel. CONCLUSION: In real-life AF patients with indication for multiple antithrombotic drugs after MI/PCI, OAC and clopidogrel was equal or better on both benefit and safety outcomes compared to triple therapy.
AB - OBJECTIVES: To investigate the risk of thrombosis and bleeding according to multiple antithrombotic treatment regimens in atrial fibrillation (AF) patients after myocardial infarction (MI) or percutaneous coronary intervention (PCI) BACKGROUND: The optimal antithrombotic treatment strategy is unresolved in patients with multiple indications. METHODS: A total of 12,165 AF patients hospitalized with MI and/or undergoing PCI between 2001-2009 were identified by nationwide registries (60.7% males, mean age 75.6 years). Risk of MI/coronary death, ischemic stroke, and bleeding according to antithrombotic treatment regimen was estimated by Cox regression models. RESULTS: Within one year, MI or coronary death, ischemic stroke, and bleeding events occurred in 2,255 (18.5%), 680 (5.6%), and 769 (6.3%) patients, respectively. Relative to triple therapy (oral anticoagulation (OAC) + aspirin + clopidogrel), no increased risk of recurrent coronary events was seen for OAC + clopidogrel (hazard ratio [HR] 0.69 [0.48-1.00]), OAC + aspirin (HR 0.96 [0.77-1.19]), or aspirin + clopidogrel (HR 1.17 [0.96-1.42]), but aspirin + clopidogrel resulted in a higher risk of ischemic stroke (HR 1.50 [1.03-2.20]). Also, OAC + aspirin and aspirin + clopidogrel were associated with a significant increased risk of all-cause death (HR 1.52 [1.17-1.99] and 1.60 [1.25-2.05]). When compared to triple therapy, bleeding risk was non-significantly reduced for OAC + clopidogrel (HR 0.78 [0.55-1.12]) and significantly reduced for OAC + aspirin and aspirin + clopidogrel. CONCLUSION: In real-life AF patients with indication for multiple antithrombotic drugs after MI/PCI, OAC and clopidogrel was equal or better on both benefit and safety outcomes compared to triple therapy.
U2 - 10.1016/j.jacc.2013.05.029
DO - 10.1016/j.jacc.2013.05.029
M3 - Journal article
C2 - 23747760
SN - 0735-1097
VL - 62
SP - 981
EP - 989
JO - American College of Cardiology. Journal
JF - American College of Cardiology. Journal
IS - 11
ER -