Key result
Triple antithrombotic therapy carries ~4-fold higher risk of major bleeding and ICH versus DOAC monotherapy.
Why the study?
The optimal dosage of direct oral anticoagulants during dual and triple antithrombotic therapy remains uncertain due to balancing ischemic and bleeding risks.
The 2020 ESC guidelines on the diagnosis and management of atrial fibrillation (AF) recommend standard dosage of direct oral anticoagulants (DOACs) during triple antithrombotic therapy (TAT). Aspirin 100 mg and the P2Y12 inhibitor clopidogrel should be preferred for dual antiplatelet therapy. Discontinuation of aspirin is recommended for subsequent dual antithrombotic therapy (DAT). Dose reduction in dabigatran (110 mg b.i.d.) and rivaroxaban (15 mg o.d.) during DAT or TAT should only be considered in patients with high bleeding risk prevailing concerns about stent thrombosis.1 While TAT is associated with a lower burden of stent thrombosis and thromboembolic events, it carries an almost four-fold increased risk for major bleeding events and intracranial haemorrhage compared with DOAC monotherapy.2 The applied treatment strategy needs to balance the ischaemic risk against the risk of bleeding in order to reach a favourable net clinical benefit. With a lacking evident decision strategy, the authors feel...
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Kazem et al. (2021) conducted an editorial in Atrial fibrillation. Triple antithrombotic therapy (TAT) vs. DOAC monotherapy was evaluated. Triple antithrombotic therapy carries an almost four-fold increased risk for major bleeding events and intracranial haemorrhage compared with DOAC monotherapy.
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