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Three-month versus twelve-month dual antiplatelet therapy after acute coronary syndrome: An updated meta-analysis of
Christopher Chinnatambi1, Abdul Rahaman Ottun1, Louise Sakowski2
1Department of Internal Medicine, Piedmont Athens Regional Medical Center, Athens, GA, United States of America.
Insights
Shorter dual antiplatelet therapy (DAPT) of 3 months significantly reduces bleeding events in acute coronary syndrome (ACS) patients after percutaneous coronary intervention (PCI) without increasing ischemic risks. This abbreviated DAPT is a safe and effective strategy.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Optimal duration of dual antiplatelet therapy (DAPT) post-acute coronary syndrome (ACS) with percutaneous coronary intervention (PCI) is debated.
- Advances in stent technology and P2Y₁₂ inhibitors necessitate re-evaluation of prolonged DAPT benefits.
- Current evidence is insufficient to guide DAPT duration in ACS patients undergoing PCI.
Purpose of the Study:
- To systematically review and meta-analyze randomized controlled trials (RCTs) comparing 3-month versus 12-month DAPT in ACS patients undergoing PCI.
- To assess the impact of abbreviated DAPT on major adverse cardiovascular and cerebrovascular events (MACCE) and clinically relevant bleeding (CRB).
- To evaluate the conclusiveness of evidence using trial sequential analysis (TSA).
Main Methods:
- Systematic review and meta-analysis of RCTs exclusively enrolling ACS patients undergoing PCI.
- Randomization to either 3-month or 12-month DAPT.
- Coprimary outcomes: MACCE and CRB. Secondary outcomes: mortality, MI, stroke, stent thrombosis, TVR, and NACE.
- Trial sequential analysis (TSA) for coprimary outcomes.
Main Results:
- Seven RCTs with 17,515 patients were included.
- 3-month DAPT showed no significant difference in MACCE compared to 12-month DAPT (RR, 0.96; 95% CI, 0.79-1.17).
- 3-month DAPT significantly reduced CRB (RR, 0.62; 95% CI, 0.50-0.76), with an absolute risk reduction of 1.9%.
- Net adverse clinical events (NACE) were lower with 3-month DAPT (RR, 0.81; 95% CI, 0.66-1.00).
- TSA confirmed conclusive evidence for reduced bleeding and futility for ischemic benefit with abbreviated DAPT.
Conclusions:
- Three-month DAPT followed by monotherapy is safe and effective in ACS patients treated with contemporary drug-eluting stents (DES).
- Abbreviated DAPT significantly reduces bleeding events without increasing ischemic complications.
- TSA supports abbreviated DAPT as a default strategy for appropriately selected ACS patients.
Background:
The optimal duration of dual antiplatelet therapy (DAPT) after acute coronary syndrome (ACS) treated with percutaneous coronary intervention (PCI) remains uncertain. Advances in stent design and the use of potent P2Y₁₂ inhibitors have reduced thrombotic risk, raising questions about whether prolonged DAPT continues to provide incremental benefit.
Methods:
We conducted a systematic review and meta-analysis of randomized controlled trials (RCTs) enrolling exclusively ACS patients undergoing PCI who were randomized to 3-month versus 12-month DAPT. Coprimary outcomes were major adverse cardiovascular and cerebrovascular events (MACCE) and clinically relevant bleeding (CRB). Secondary outcomes included all-cause mortality, myocardial infarction, stroke, stent thrombosis, target-vessel revascularization, and net adverse clinical events (NACE; MACCE + CRB). Trial sequential analysis (TSA) was performed to evaluate the conclusiveness of evidence for each coprimary outcome.
Results:
Seven RCTs encompassing 17,515 patients (mean age 63 years; 31% women; 45% STEMI) were included. Abbreviated 3-month DAPT did not differ from 12-month therapy for MACCE (5.6% vs 5.7%; risk ratio [RR], 0.96; 95% CI, 0.79-1.17; I2 = 44%), but significantly reduced CRB (3.0% vs 4.9%; RR, 0.62; 95% CI, 0.50-0.76; I2 = 31%), corresponding to an absolute risk reduction of 1.9% and number needed to treat of 52. NACE was lower with abbreviated therapy (7.9% vs 9.7%; RR, 0.81; 95% CI, 0.66-1.00). TSA crossed the futility boundary for MACCE and the benefit boundary for CRB, indicating conclusive evidence for bleeding reduction and futility for ischemic benefit.
Conclusions:
Among ACS patients treated with contemporary DES, 3-month DAPT followed by monotherapy significantly reduces bleeding without increasing ischemic events. TSA confirms the conclusiveness of current evidence, supporting abbreviated DAPT as a safe and effective default strategy in appropriately selected ACS patients.
Registration:
The protocol was registered in the International Prospective Register of Systematic Reviews (PROSPERO) with unique identifier CRD420251143351 and URL: https://www.crd.york.ac.uk/prospero/search.
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