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Bleeding and ischaemic outcomes in patients treated with dual or triple antithrombotic therapy: systematic review and
Paul M Haller1,2, Patrick Sulzgruber3, Christoph Kaufmann4
1Department of General and Interventional Cardiology, University Heart Center Hamburg Eppendorf, Hamburg, Germany.
Insights
Dual antithrombotic therapy (DAT) significantly reduces bleeding in atrial fibrillation patients after PCI compared to triple antithrombotic therapy (TAT). DAT showed similar effectiveness in preventing ischemic events, making it a safer alternative for these patients.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Patients with atrial fibrillation (AF) undergoing percutaneous coronary intervention (PCI) often receive triple antithrombotic therapy (TAT) combining oral anticoagulation, a P2Y12 inhibitor, and aspirin.
- This TAT regimen is associated with a high risk of bleeding complications.
- Dual antithrombotic therapy (DAT), omitting aspirin, is a potential alternative to reduce bleeding but its ischemic risk is not well-defined.
Purpose of the Study:
- To systematically review and analyze randomized controlled trials comparing DAT with TAT in patients with AF following PCI and/or acute coronary syndrome (ACS).
- To evaluate the efficacy and safety of DAT versus TAT in terms of bleeding and ischemic events.
Main Methods:
- A meta-analysis of four randomized controlled trials involving 9317 patients (5039 on DAT, 4278 on TAT).
- Comparison of major bleeding events, composite ischemic endpoints, myocardial infarction (MI), and stent thrombosis between DAT and TAT groups.
- Statistical analysis using hazard ratios (HR) and 95% confidence intervals (CI).
Main Results:
- DAT significantly reduced Thrombolysis in Myocardial Infarction (TIMI) major bleeding (HR 0.52, P=0.0001).
- There was no significant difference in the composite ischemic endpoint between DAT and TAT (HR 0.98, P=0.88).
- Rates of myocardial infarction (MI) and stent thrombosis were not significantly different between the two groups.
Conclusions:
- Dual antithrombotic therapy (DAT) is associated with significantly lower bleeding rates compared to triple antithrombotic therapy (TAT) in AF patients post-PCI or ACS.
- DAT appears to have a similar efficacy to TAT in preventing ischemic endpoints.
- Further research is warranted to assess DAT's applicability in high-risk ischemic patient populations.
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.
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