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


Journal

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions
ISSN: 1522-726X
Titre abrégé: Catheter Cardiovasc Interv
Pays: United States
ID NLM: 100884139

Informations de publication

Date de publication:
01 Jul 2019
Historique:
received: 07 11 2018
accepted: 02 12 2018
pubmed: 19 1 2019
medline: 4 8 2020
entrez: 19 1 2019
Statut: ppublish

Résumé

To investigate the use of prasugrel after percutaneous coronary intervention (PCI) in African American (AA) patients presenting with acute coronary syndrome (ACS). AA patients are at higher risk for adverse cardiovascular outcomes after PCI and may derive greater benefit from the use of potent antiplatelet therapy. 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. 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. 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.

Sections du résumé

OBJECTIVE OBJECTIVE
To investigate the use of prasugrel after percutaneous coronary intervention (PCI) in African American (AA) patients presenting with acute coronary syndrome (ACS).
BACKGROUND 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 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 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 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.

Identifiants

pubmed: 30656812
doi: 10.1002/ccd.28033
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0
Clopidogrel A74586SNO7
Prasugrel Hydrochloride G89JQ59I13

Types de publication

Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

53-60

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Michela Faggioni (M)

Icahn School of Medicine at Mount Sinai, New York, New York.
James J Peters Veterans Affairs Medical Center, Bronx, New York.

Usman Baber (U)

Icahn School of Medicine at Mount Sinai, New York, New York.

Jaya Chandrasekhar (J)

Icahn School of Medicine at Mount Sinai, New York, New York.

Samantha Sartori (S)

Icahn School of Medicine at Mount Sinai, New York, New York.

William Weintraub (W)

Christiana Care Health System, Newark, Delaware.

Sunil V Rao (SV)

The Duke Clinical Research Institute, Durham, North Carolina.

Birgit Vogel (B)

Icahn School of Medicine at Mount Sinai, New York, New York.

Bimmer Claessen (B)

Icahn School of Medicine at Mount Sinai, New York, New York.

Annapoorna Kini (A)

Icahn School of Medicine at Mount Sinai, New York, New York.

Mark Effron (M)

John Ochsner Heart and Vascular Institute, Ochsner Medical Center, New Orleans, Louisiana.
Eli Lilly and Company, Indianapolis, Indiana.

Zhen Ge (Z)

Icahn School of Medicine at Mount Sinai, New York, New York.

Stuart Keller (S)

Eli Lilly and Company, Indianapolis, Indiana.

Craig Strauss (C)

Minneapolis Heart Institute, Minneapolis, Minnesota.

Clayton Snyder (C)

Icahn School of Medicine at Mount Sinai, New York, New York.

Catalin Toma (C)

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

Sandra Weiss (S)

Christiana Care Health System, Newark, Delaware.

Melissa Aquino (M)

Icahn School of Medicine at Mount Sinai, New York, New York.

Brian Baker (B)

Daiichi-Sankyo, Inc, Parsippany, New Jersey.

Anthony Defranco (A)

Aurora Cardiovascular Services, Milwaukee, Wisconsin.

Sameer Bansilal (S)

Icahn School of Medicine at Mount Sinai, New York, New York.

Brent Muhlestein (B)

Intermountain Heart Institute, Salt-Lake city, Utah.

Samir Kapadia (S)

Cleveland Clinic, Cleveland, Ohio.

Stuart Pocock (S)

London School of Hygiene and Tropical Medicine, London, United Kingdom.

Kanhaiya L Poddar (KL)

Cleveland Clinic, Cleveland, Ohio.

Timothy D Henry (TD)

Cedars-Sinai Heart Institute, Los Angeles, California.

Roxana Mehran (R)

Icahn School of Medicine at Mount Sinai, New York, New York.

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Classifications MeSH