De-escalating Dual Antiplatelet Therapy to Ticagrelor Monotherapy in Acute Coronary Syndrome : A Systematic Review and Individual Patient Data Meta-analysis of Randomized Clinical Trials.
Summary
Across 9,130 ACS patients in three RCTs, ticagrelor monotherapy after short DAPT reduced major bleeding (BARC 3/5; HR 0.30) without increasing ischemic events (HR 0.85) compared with 12 months of ticagrelor-based DAPT. Benefits were consistent across STEMI, NSTEMI, and unstable angina.
Key Findings
- Individual patient data from 3 RCTs (TICO, T-PASS, ULTIMATE-DAPT) totaling 9,130 ACS patients were analyzed.
- Primary ischemic outcome rates were similar with ticagrelor monotherapy vs. standard DAPT (1.7% vs 2.1%; HR 0.85, 95% CI 0.63–1.16).
- Major bleeding (BARC 3/5) was significantly lower with ticagrelor monotherapy (0.8% vs 2.5%; HR 0.30, 95% CI 0.21–0.45).
- Effects were consistent across STEMI, NSTEMI, and unstable angina subgroups.
- PROSPERO-registered analysis; no external funding reported.
Clinical Implications
Clinicians can consider early transition to ticagrelor monotherapy after a short DAPT course in ACS patients post-DES to reduce major bleeding risk without compromising ischemic protection, tailoring duration to patient risk.
Why It Matters
Provides high-quality, IPD-based evidence supporting DAPT de-escalation to ticagrelor monotherapy after DES in ACS, with clear bleeding reduction and no ischemic penalty, informing guideline updates.
Limitations
- Only ticagrelor-based de-escalation was assessed; other P2Y12 strategies not included.
- Trials largely conducted in East Asian populations, potentially limiting global generalizability.
Future Directions
Head-to-head comparisons of alternative de-escalation strategies, incorporation of bleeding/ischemia risk scores for individualized DAPT duration, and validation across diverse global populations.
Study Information
- Study Type
- Meta-analysis
- Research Domain
- Treatment
- Evidence Level
- I - Synthesis of randomized controlled trials with individual patient data
- Study Design
- OTHER