About this trial
Monotherapy with a P2Y12 inhibitor after a minimum period of DAPT following percutaneous coronary intervention (PCI) is an emerging de-escalation antiplatelet strategy in recent years. However, the optimal timing for de-escalating DAPT in ACS patients undergoing PCI remains debated. The OPT-CAD score is a risk stratification tool derived from Chinese patients which has been demonstrated superior predictive capabilities for ischemic events and all-cause mortality than the GRACE score. Therefore, we hypothesize that the OPT-CAD score can be used to guide the timing of the DAPT de-escalation strategy to monotherapy with P2Y12 inhibitors for ACS patients, that is, low-risk patients could be de-escalated after 1 month, while high-risk patients could be de-escalated after 3 months, so as to achieve individualized antithrombotic therapy and maximize patient benefit.
Eligibility criteria
Qualifiers
Adult patients with ages of 18-80 years;
Patients with clinically diagnosed ACS who have undergone at least one DES implantation;
Individuals capable of completing the OPT-CAD scoring calculation;
Researchers assessing that participants can tolerate at least a 12-month duration of DAPT therapy;
Disqualifiers
Left main coronary artery lesion PCI;
Allergy to study drugs such as aspirin, clopidogrel, or ticagrelor;
Meeting 1 major or 2 minor criteria for high bleeding risk according to the ARC-HBR criteria;
Anticipated need for revascularization or surgical intervention within 12 months;
Trial design
Treatments tested in this trial
- standard DAPT
- OPT-CAD score guided DAPT de-escalation