scholarly journals Triple antithrombotic therapy in patients with atrial fibrillation undergoing coronary artery stenting: hovering among bleeding risk, thromboembolic events, and stent thrombosis

2012 ◽  
Vol 10 (1) ◽  
pp. 22 ◽  
Author(s):  
Mila Menozzi ◽  
Andrea Rubboli ◽  
Antonio Manari ◽  
Rossana De Palma ◽  
Roberto Grilli
2019 ◽  
Vol 76 (18) ◽  
pp. 1395-1402
Author(s):  
Jordan L Lacoste ◽  
Cory L Hansen

Abstract Purpose Updates to the primary literature and clinical practice guidelines on use of antithrombotic combinations for patients with atrial fibrillation (AF) undergoing percutaneous coronary intervention (PCI) and stenting are reviewed. Summary Up to 8% of patients undergoing PCI have AF and thus require both antiplatelet and anticoagulation therapies, which put them at increased risk for bleeding. Current literature suggests that using a single antiplatelet agent in combination with oral anticoagulation with a direct-acting oral anticoagulant (i.e., dual therapy) is effective and associated with less bleeding risk than triple therapy (dual antiplatelet therapy plus an oral anticoagulant) in patients with AF undergoing PCI with stent placement. The most recently studied dual therapy regimens consist of clopidogrel in combination with apixaban, rivaroxaban, or dabigatran. Guidelines recommend use of an oral anticoagulant plus clopidogrel and aspirin for a short period of time. In general, aspirin should be discontinued in most patients at discharge. In patients with a high risk of thrombosis, aspirin can be continued for up to 1 month. Dual therapy should be continued for 12 months, with oral anticoagulant monotherapy continued thereafter. Conclusion A review of current literature on antithrombotic therapy in patients with AF undergoing PCI and subsequent coronary artery stenting indicates that the favored regimen is dual therapy consisting of clopidogrel with rivaroxaban, apixaban, dabigatran, or a vitamin K antagonist. Aspirin may be used in the periprocedural period but should be discontinued thereafter to reduce the risk of bleeding. Decisions regarding specific agents and duration of treatment should be based on thrombotic risk, bleeding risk, and patient preference.


2019 ◽  
Vol 5 (4) ◽  
pp. 226-236 ◽  
Author(s):  
Paul M Haller ◽  
Patrick Sulzgruber ◽  
Christoph Kaufmann ◽  
Bastiaan Geelhoed ◽  
Juan Tamargo ◽  
...  

Abstract Aims The combination of oral anticoagulation with a P2Y12 inhibitor and aspirin in patients with atrial fibrillation (AF) undergoing percutaneous coronary intervention (PCI) is associated with a high bleeding risk. Dual antithrombotic therapy (DAT) with omission of aspirin is a promising option to reduce bleedings, but carries a yet unknown risk of ischaemic events. We therefore sought to systematically review and analyse randomized controlled trials investigating DAT vs. triple antithrombotic therapy (TAT) in patients with AF following PCI and/or acute coronary syndrome (ACS). Methods and results We included four trials with overall 9317 patients (5039 DAT, 4278 TAT) in our analysis. Dual antithrombotic therapy was associated with a significant reduction in thrombolysis in myocardial infarction major bleeding [hazard ratio (HR) 0.52, 95% confidence interval (CI) 0.42–0.65; P = 0.0001], while the composite trial-defined ischaemic endpoint did not differ significantly between DAT and TAT (HR 0.98, 95% CI 0.79–1.22; P = 0.88). There was also no difference regarding the occurrence of myocardial infarction (MI; HR 1.16, 95% CI 0.92–1.46; P = 0.21) or stent thrombosis (HR 1.25, 95% CI 0.69–2.26; P = 0.46). Absolute numbers for MI were 131/4278 (3.1%) with TAT and 182/5039 (3.6%) with DAT, and for stent thrombosis 32/4278 (0.75%) and 52/5039 (1%), respectively. A post hoc power calculation based on the size and event rate of this meta-analysis revealed 80% power to detect a 37% and 100% increase in MI and stent thrombosis, respectively. Conclusion Dual antithrombotic therapy significantly reduces bleedings compared with TAT and seems to have a similar effect in preventing ischaemic endpoints in AF patients post-PCI or ACS. Future investigations are needed to determine its applicability specifically in patients at high risk of ischaemic outcomes.


Circulation ◽  
2010 ◽  
Vol 121 (18) ◽  
pp. 2067-2070 ◽  
Author(s):  
Jeremy S. Paikin ◽  
Douglas S. Wright ◽  
Mark A. Crowther ◽  
Shamir R. Mehta ◽  
John W. Eikelboom

2015 ◽  
Vol 1 (1) ◽  
pp. 5 ◽  
Author(s):  
Andrew Owen

<p><span>Background: </span>Patients with atrial fibrillation and a coronary artery stent require anticoagulation to provide prophylaxis</p><p>against stroke and dual antiplatelet therapy to provide prophylaxis against stent thrombosis (triple therapy).</p><p>This combination increases the risk of major bleeding complications compared to either treatment alone. It is</p><p>suggested that an alternative to triple therapy is high dose dual antiplatelet therapy (aspirin 325mg/day and</p><p>clopidogrel 75 mg/day), which would have similar efficacy to triple therapy in relation to prophylaxis against</p><p>both stroke and stent thrombosis with a lower risk of bleeding complications.</p><p><span>Summary: </span>1. Patients with atrial fibrillation and a coronary artery stent require triple therapy, which is associated with</p><p>increased bleeding risk.</p><p>2. In everyday practice 50% of patients do not receive this, because of the excess bleeding risk.</p><p>3. It is suggested that for patients at increased bleeding risk and for whom it is felt that triple therapy is not</p><p>suitable, Aspirin (325mg daily) and clopidogrel (75mg daily) should be considered.</p><p> </p>


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