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In a multicenter trial sponsored by the manufacturer of the P2Y12 inhibitor ticagrelor (NCT02270242), researchers compared 1-year outcomes with two treatment regimens after percutaneous coronary intervention (PCI). The 9006 patients had both high-risk clinical and angiographic features for bleeding or ischemic events, received a drug-eluting stent (DES), and were treated for 3 months with ticagrelor plus aspirin.
At 3 months, 7119 patients underwent randomization (mean age, 65; diabetes, 37%; PCI for acute coronary syndrome, 65%) to continue this regimen or to receive ticagrelor alone. The primary endpoint — major bleeding types 2, 3, or 5, as defined by the Bleeding Academic Research Consortium, from randomization to 1 year later — occurred…