Use of prasugrel and clinical outcomes in African-American patients treated with percutaneous coronary intervention for acute coronary syndromes.

Michela Faggioni ORCID logo; Usman Baber; Jaya Chandrasekhar ORCID logo; Samantha Sartori; William Weintraub; Sunil V Rao; Birgit Vogel; Bimmer Claessen; Annapoorna Kini ORCID logo; Mark Effron ORCID logo; +16 more... Zhen Ge; Stuart Keller; Craig Strauss; Clayton Snyder; Catalin Toma; Sandra Weiss; Melissa Aquino; Brian Baker; Anthony Defranco; Sameer Bansilal; Brent Muhlestein; Samir Kapadia ORCID logo; Stuart Pocock; Kanhaiya L Poddar; Timothy D Henry ORCID logo; Roxana Mehran; (2019) Use of prasugrel and clinical outcomes in African-American patients treated with percutaneous coronary intervention for acute coronary syndromes. Catheterization and Cardiovascular Interventions, 94 (1). pp. 53-60. ISSN 1522-1946 DOI: 10.1002/ccd.28033
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OBJECTIVE: To investigate the use of prasugrel after percutaneous coronary intervention (PCI) in African American (AA) patients presenting with acute coronary syndrome (ACS). BACKGROUND: AA patients are at higher risk for adverse cardiovascular outcomes after PCI and may derive greater benefit from the use of potent antiplatelet therapy. METHODS: Using the multicenter PROMETHEUS observational registry of ACS patients treated with PCI, we grouped patients by self-reported AA or other races. Clinical outcomes at 90-day and 1-year included non-fatal myocardial infarction (MI), major adverse cardiac events (composite of death, MI, stroke, or unplanned revascularization) and major bleeding. RESULTS: The study population included 2,125 (11%) AA and 17,707 (89%) non-AA patients. AA patients were younger, more often female (46% vs. 30%) with a higher prevalence of diabetes mellitus, chronic kidney disease, and prior coronary intervention than non-AA patients. Although AA patients more often presented with troponin (+) ACS, prasugrel use was much less common in AA vs. non-AA (11.9% vs. 21.4%, respectively, P = 0.001). In addition, the use of prasugrel increased with the severity of presentation in non-AA but not in AA patients. Multivariable logistic regression showed AA race was an independent predictor of reduced use of prasugrel (0.42 [0.37-0.49], P < 0.0001). AA race was independently associated with a significantly higher risk of MI at 90-days and 1 year after PCI. CONCLUSIONS: Despite higher risk clinical presentation and worse 1-year ischemic outcomes, AA race was an independent predictor of lower prasugrel prescription in a contemporary population of ACS patients undergoing PCI.


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