Key result
Double therapy with direct oral anticoagulants significantly reduced the risk of ISTH major or clinically relevant nonmajor bleeding (RR 0.65) compared to triple therapy with vitamin K antagonists in patients with atrial fibrillation undergoing percutaneous coronary intervention.
Why the study?
Patients with atrial fibrillation undergoing PCI require optimal antithrombotic therapy balancing bleeding and ischemic risks, but the safety and efficacy of DOAC double therapy versus VKA triple therapy needed systematic evaluation.
Meta-Analysis (n=6,733)
Mixed (three open-label, one placebo-controlled)
Randomized (included studies)
Yes
Relative Risk: 0.65 (95% CI 0.48–0.88)
Absolute Event Rate: 14.2% vs 21.5%
p-value: p=<0.00001
Supports DOAC double therapy to reduce bleeding in AF-PCI; confirms no efficacy loss versus VKA triple across 4 RCTs.
Background Atrial fibrillation (AF) and coronary artery disease (CAD) are commonly associated. Cotreatment with multiple antithrombotic agents can increase the risk of bleeding. We sought to evaluate patient‐centered outcomes in patients with AF on double therapy with direct oral anticoagulants (DOACs) compared to patients with standard triple therapy, [a vitamin K antagonist (VKA) plus dual antiplatelet therapy]. Methods We performed a literature search of randomized controlled trials (RCTs) reporting outcomes of patients receiving double therapy with DOACs compared to triple therapy with VKAs in patients with AF undergoing percutaneous coronary intervention (PCI). Patient‐centered outcomes were the International Society of Thrombosis and Hemostasis (ISTH) major or clinically relevant nonmajor bleeding (CRNB), all‐cause mortality, major adverse cardiovascular events (MACE), stent thrombosis, myocardial infarction, and stroke. Results Four RCTs (9602 patients) met our inclusion criteria. Compared to VKAs, DOACs were associated with significantly lower ISTH major bleeding/ CRNB (RR: 0.75, 95% CI: 0.67‐0.82, P < .00001, I2 = 11%). There were no statistically significant differences in the efficacy outcomes, including myocardial infarction (RR: 0.99, 95% CI :0.79‐1.25, P = .96), stent thrombosis (RR: 0.97, 95% CI: 0.6‐1.55, P = .89), ischemic stroke (RR: 0.76, 95% CI: 0.5‐1.15, P = .19), all‐cause mortality (RR: 1.06, 95% CI: 0.85‐1.31, P = .61), and MACE (RR: 1.06, 95% CI: 0.91‐1.22, P = .97). Conclusion Compared with triple therapy with VKAS, double therapy with DOACs is associated with a reduced risk of bleeding and is as effective in patients with AF undergoing PCI.
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Agasthi et al. (2020) conducted a meta-analysis in Atrial fibrillation and percutaneous coronary intervention (n=6,733). Direct oral anticoagulants (DOAC) plus P2Y12 inhibitor (double therapy) vs. Vitamin K antagonist (VKA) plus dual antiplatelet therapy (triple therapy) was evaluated on ISTH major or clinically relevant nonmajor bleeding (RR 0.65, 95% CI 0.48-0.88, p=<0.00001). Double therapy with direct oral anticoagulants significantly reduced the risk of ISTH major or clinically relevant nonmajor bleeding (RR 0.65) compared to triple therapy with vitamin K antagonists in patients with atrial fibrillation undergoing percutaneous coronary intervention.
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