
Discontinuation of aspirin at 90 days following stenting and continuing on P2Y12 inhibitor monotherapy, was not associated with increased rates of death from any cause, heart attack, or stroke after one year, according to a new study presented at the American College of Cardiology Annual Scientific Sessions in New Orleans.
Researchers for the SMART-CHOICE trial enrolled 2,993 patients who underwent percutaneous coronary intervention (PCI) and received a cobalt chromium everolimus-eluting eluting stent. Patients were randomly assigned to receive either standard dual antiplatelet therapy (DAPT) or aspirin plus a P2Y12 inhibitor (clopidogrel, prasugrel, or ticagrelor) for the first three months and then just the P2Y12 inhibitor by itself for the remaining nine months. The primary endpoint was a composite of major adverse cardiac and cerebrovascular events (MACCE; all-cause death, myocardial infarction, or stoke at 12 months after index procedure).
According to the study results, there was no difference in the primary study endpoint of MACCE rate (2.9% P2Y12 inhibitor vs. 2.5% DAPT; HR=1.19; 95% CI, 0.76 to 1.85; P-0.46; P=0.007 for noninferiority). There was no observed difference between the study groups at 90 days (HR=1.31; 95% CI, 0.57 to 2.98; P=0.52) and at one year (HR=1.14; 95% CI, 0.67 to 1.93; P=0.63). There was a small advantage for patients assigned to P2Y12 inhibitor monotherapy at one year in terms of BARC type 2-5 bleeding (P=0.02), with a similar finding in the per protocol analysis (P=0.04).