Coronary disease & ACSSecondary analysis

Potent P2Y12 Inhibitor Monotherapy vs Dual Antiplatelet Therapy (DAPT) After PCI in Patients With and Without STEMI

J Am Coll CardiolPublished

  • Prespecified subgroup analysis of the NEO-MINDSET randomised trial

Authors' conclusion

In patients with STEMI treated with percutaneous coronary intervention, early aspirin withdrawal may be harmful, because it increases the risk of ischemic events. Conversely, in NSTE-ACS, potent P2Y12 inhibitor monotherapy may be a viable therapeutic option: Ischemic event rates were similar and bleeding was reduced compared with DAPT.

Study context

Population
Acute coronary syndrome (ACS) patients undergoing PCI, by presentation: STEMI or NSTE-ACS (unstable angina or NSTEMI; n = 1,291)STEMI 2,119
Participants
3,410 patients
Comparison
Potent P2Y12 inhibitor monotherapy vs DAPT, by STEMI vs NSTE-ACS presentation
Primary endpoint
Co-primary: ischemic composite (all-cause death, MI, stroke, urgent target vessel revascularization) and BARC type 2, 3 or 5 bleeding
Follow-up
1 year

Primary result

As reported in the abstract

Co-primary ischemic composite, by presentation
Monotherapy vs DAPTHazard ratio (95% CI)
STEMI: 8.2% vs 5.2%
1.60(1.14–2.24)
NSTE-ACS: 5.1% vs 6.0%
0.84(0.53–1.35)

Safety

OutcomeHR (95% CI)
Co-primary BARC type 2, 3 or 5 bleeding, by presentation — Monotherapy vs DAPT · STEMI0.37 (0.22–0.61)
Co-primary BARC type 2, 3 or 5 bleeding, by presentation — Monotherapy vs DAPT · NSTE-ACS0.45 (0.23–0.86)
  • Co-primary BARC type 2, 3 or 5 bleeding, by presentation: P for interaction = 0.650

Original publication

Potent P2Y12 Inhibitor Monotherapy vs DAPT After PCI in Patients With and Without STEMI. J Am Coll Cardiol. Published 18 November 2025. doi:10.1016/j.jacc.2025.10.058

Summarised from the published abstract; every number is checked against it