TADCLOT- a Double Blind Randomized Controlled Trial

Following primary percutaneous coronary intervention (PCI) for acute ST elevation myocardial infarction (STEMI), there persists an elevated risk of adverse events. Recent American College of Cardiology National cath data registry underscores the severity of this issue, revealing a substantial cumulative death rate of 18.5% and a major adverse cardiac events (MACE) risk of 24.4% within the first year of PCI. The critical first 30 days of PCI present a heightened susceptibility to stent thrombosis (ST), particularly in patients with STEMI, thereby necessitating vigilant clinical oversight. Based on the clinical presentation, the risk of ST within the first month varies such that patients with myocardial infarction have a 4.5 fold higher risk compared to non ACS patients. After 30 days, the risk of ST continues to progressively go down such that there is no longer a differences in the risk of ST between ACS and non ACS patients. Additionally, an elevated ST risk in patients with MI within 30 days is largely confined to those with high platelet reactivity (which is significantly more prevalent in ACS patients) on Clopidogrel (HR: 5.77; 95% CI: 2.13 to 15.63; p= 0.001).

The substantial challenges faced by post- primary PCI patients are further underscored by the national institute of cardiovascular diseases (NICVD) data, which has emerged as the world's largest primary PCI center. A reported stent thrombosis rate of 4.9% correlates with a considerable risk of morbidity and mortality, approximating 40%. Additionally, randomized clinical trials have reported mortality rates as high as 50% in patients with early (within 1 month of the procedure) stent thrombosis.

While randomized trials have demonstrated the superior efficacy of Ticagrelor over Clopidogrel in high-risk STEMI cohort enshrining them in current practice guidelines, pragmatic clinical practices persist in favoring the routine utilization of Clopidogrel, primarily due to economic considerations. This deviation from evidence-based recommendations is exacerbated by the widespread adoption of a twice-daily Clopidogrel regimen, substantiated by post hoc analyses indicating enhanced outcomes at thirty days compared to a once-daily standard dose. Meta-analytical evidence further supports this approach, revealing a significant reduction in adverse events with a 150mg dose of Clopidogrel, albeit accompanied by a marginal increase in the risk of minor bleeding. Interestingly, there is dearth of randomized evaluation of the more potent P2Y12 inhibitors including Ticagrelor against a twice daily Clopidogrel regimen, underscoring the need for rigorous scientific scrutiny. Complicating this landscape is the disproportionately higher prevalence of CYP2C19 mutations among South Asian populations, contributing to a nearly six fold increased risk of Clopidogrel non-responsiveness and a three folds higher odds of recurrent MI.