Key result
Double therapy matches triple therapy for MACE in AF PCI, reducing bleeding but increasing stent thrombosis.
Why the study?
Prior randomized controlled trials evaluating optimal antithrombotic therapies for patients with AF undergoing PCI have not been powered to evaluate ischemic outcomes.
Does double therapy reduce bleeding and ischemic events compared to triple therapy in patients with atrial fibrillation undergoing PCI?
Systematic Review (n=10,238)
Does double therapy reduce bleeding and ischemic events compared to triple therapy in patients with atrial fibrillation undergoing PCI?
In patients with AF undergoing PCI, double antithrombotic therapy significantly reduces bleeding risk compared to triple therapy, though it may carry a modestly increased risk of stent thrombosis.
Answers are grounded in this paper and cite their sources.
Supports double therapy to cut bleeding in AF patients post-PCI; extends prior RCTs by quantifying modest stent thrombosis increase.
Background Prior randomized controlled trials (RCT) evaluating the optimal antithrombotic therapies for patients with atrial fibrillation (AF) undergoing percutaneous coronary intervention (PCI) have not been powered to evaluate ischemic outcomes. We compared double therapy with oral anticoagulation (OAC) and a P2Y12 inhibitor to triple therapy with an OAC + dual antiplatelet therapy in patients with AF requiring PCI. Methods Using PRISMA guidelines, we searched for RCTs including patients with AF as an indication for OAC and undergoing PCI or medical management of acute coronary syndrome. The results were pooled using fixed‐effects and random‐effects models to estimate the overall effect of double therapy versus triple therapy on ischemic and bleeding outcomes. Results We identified four RCTs, comprising 10,238 patients (5,498 double therapy, 4,740 triple therapy). Trial‐reported major adverse cardiovascular events were similar between double therapy and triple therapy (fixed effect model OR 1.09, 95% CI 0.94–1.26). However, stent thrombosis (61/5,496 double therapy vs. 33/4738 triple therapy; fixed effect model OR 1.57, 95% CI 1.02–2.40; number needed to treat with triple therapy = 242) favored triple therapy. Bleeding outcomes were less frequent with double therapy (746/5470 vs. 950/4710; fixed effect model OR 0.59, 95% CI 0.53–0.65; number needed to harm with triple therapy = 16), but with significant heterogeneity (Q = 8.33, p = .04; I2 = 64%), as were intracranial hemorrhages (19/5470 vs. 30/4710; fixed effect model OR 0.54, 95% CI 0.31–0.96). Conclusions Double therapy in patients with AF requiring OAC following PCI or Acute coronary syndrome has a significantly better safety profile than triple therapy but may be associated with a modest increased risk of stent thrombosis.
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Sullivan et al. (2019) conducted a systematic review in Atrial fibrillation requiring percutaneous coronary intervention or medical management of acute coronary syndrome (n=10,238). Double therapy (oral anticoagulation and a P2Y12 inhibitor) vs. Triple therapy (oral anticoagulation + dual antiplatelet therapy) was evaluated on Trial-reported major adverse cardiovascular events (OR 1.09, 95% CI 0.94-1.26). Double therapy in patients with AF undergoing PCI showed similar MACE rates to triple therapy (OR 1.09; 95% CI 0.94-1.26), with significantly less bleeding but a higher risk of stent thrombosis.
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