Key result
Triple antithrombotic therapy increases bleeding ~110% vs. DAPT without reducing ischemic outcomes.
Why the study?
Current guidelines supporting prophylactic oral anticoagulation after anterior STEMI are based on limited evidence, and the balance between thromboembolic prevention and bleeding risk remains uncertain.
Does triple antithrombotic therapy reduce ischemic events or increase bleeding compared to dual antiplatelet therapy alone in patients with anterior STEMI undergoing pPCI?
Systematic Review and Meta-Analysis (n=3,692)
Does triple antithrombotic therapy reduce ischemic events or increase bleeding compared to dual antiplatelet therapy alone in patients with anterior STEMI undergoing pPCI?
Relative Risk: 2.1 (95% CI 1.6–2.76)
p-value: p=<0.0001
Routine prophylactic triple antithrombotic therapy following anterior STEMI significantly increases bleeding risk without a demonstrable ischemic benefit compared to DAPT alone.
Avoids excess bleeding without ischemic gain in anterior STEMI; challenges routine prophylactic triple therapy over DAPT.
Background Left ventricular thrombus (LVT) remains an important complication following anterior ST-elevation myocardial infarction (STEMI), despite widespread adoption of primary percutaneous coronary intervention (pPCl). Current guidelines supporting prophylactic oral anticoagulation in high-risk patients are based on limited evidence, and the balance between thromboembolic prevention and bleeding risk remains uncertain. PubMed, Embase and etc were searched for studies comparing triple antithrombotic therapy (TAPT; anticoagulation plus DAPT) versus DAPT alone in patients with anterior STEMI undergoing pPCI. Random-effects model was used to pool risk ratios with 95% confidence intervals (CI). Outcomes included mortality, bleeding, LVT, and etc. Main Text 7 studies including 3,692 participants were included. TAPT was associated with a significantly increased risk of bleeding compared with DAPT alone (RR: 2.10; 95% CI: 1.60-2.76; P<0.0001; I 2 =0%). No significant differences were observed in all-cause mortality (RR: 1.05; 95% CI: 0.54-2.04; P=0.89; I 2 =39%), recurrent myocardial infarction (RR: 1.52; 95% CI: 0.94-2.45; P=0.09; I 2 =0%), stroke (RR: 0.86; 95% CI: 0.20-3.73; P=0.84; I 2 =55%), LVT formation (RR: 0.54; 95% Cl: 0.21-1.40; P=0.21; l 2 =61%), NACE (RR: 0.93; 95% CI: 0.49-1.75; P=0.82; I 2 =77%), or embolic events (RR: 0.53; 95% CI: 0.21-1.33; P=0.18; I 2 =0%). Conclusions TAPT significantly increased bleeding risk compared with DAPT. No significant reductions were observed in ischemic outcomes; however, wide confidence intervals indicate limited precision and do not exclude a clinically meaningful benefit or harm. Current evidence therefore does not support routine prophylactic TAPT, and adequately powered contemporary randomised trials are needed.
No takes yet. Share an insight, caveat, or question.
Ahsan et al. (2026) conducted a systematic review and meta-analysis in Anterior STEMI (n=3,692). Triple antithrombotic therapy (TAPT) vs. Dual antiplatelet therapy (DAPT) alone was evaluated on Bleeding (RR 2.10, 95% CI 1.60-2.76, p=<0.0001). Triple antithrombotic therapy significantly increased the risk of bleeding compared with DAPT alone (RR 2.10; 95% CI 1.60-2.76; P<0.0001) without significantly reducing ischemic outcomes.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: