Comparative efficacy and safety of de-escalation, abbreviation, and standard potent P2Y12 inhibitor–based dual antiplatelet therapy strategies after acute coronary syndrome: a network meta-analysis

EHJ - Open

14 October 2026
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ESC Journals CARDIOVASCULAR PHARMACOLOGY Interventional Cardiology

Abstract

AbstractAims

Potent P2Y12 inhibitor-based dual antiplatelet therapy (DAPT) is the default antiplatelet strategy after acute coronary syndrome (ACS), though de-escalation to clopidogrel-based DAPT and abbreviated DAPT followed by potent P2Y12 inhibitor monotherapy are increasingly adopted to mitigate bleeding risk. However, their relative efficacy and safety remain uncertain.

Methods and results

Network meta-analyses of randomized controlled trials were performed to compare three guideline-endorsed strategies: (i) short-term potent P2Y12 inhibitor-based DAPT de-escalation to clopidogrel-based DAPT, (ii) abbreviated DAPT followed by potent P2Y12 inhibitor monotherapy, and (iii) standard 12-month potent P2Y12 inhibitor-based DAPT. The primary efficacy endpoint was major adverse cardiovascular events (MACE). Secondary efficacy endpoints included all-cause mortality, cardiovascular mortality, myocardial infarction, stent thrombosis, and stroke. The primary safety endpoint was major bleeding. The key net clinical endpoint was net adverse clinical events (NACE). PROSPERO (CRD420251144892) Seven randomized controlled trials involving 20 673 patients were included. Both the de-escalation and abbreviation strategies significantly reduced major bleeding (RR 0.43, 95% CI 0.25–0.74, P = 0.002; and RR 0.43, 95% CI 0.33–0.58, P < 0.001, respectively) and NACE (RR 0.54, 95% CI 0.41–0.70, P < 0.001; and RR 0.72, 95% CI 0.61–0.84, P < 0.001, respectively) without increasing MACE or other ischaemic outcomes. Indirect comparison indicated that de-escalation vs. abbreviation strategies demonstrated comparable MACE, NACE, and bleeding outcomes.

Conclusion

Following ACS, both de-escalation to clopidogrel-based DAPT and abbreviated DAPT followed by potent P2Y12 inhibitor monotherapy effectively reduce bleeding risk without compromising ischaemic protection. Given that the only available comparison between the two simplified strategies was indirect and showed comparable MACE and NACE outcomes, further research is warranted to determine the optimal individualized approach.

Contributors

Chi-Sheng Hung
Chi-Sheng Hung

Author

National Taiwan University Hospital Taipei , Taiwan