Antithrombotic Therapy in Patients With Atrial Fibrillation Treated With Oral Anticoagulation Undergoing Percutaneous Coronary Intervention: A North American Perspective: 2021 Update.


Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
09 02 2021
Historique:
entrez: 8 2 2021
pubmed: 9 2 2021
medline: 22 12 2021
Statut: ppublish

Résumé

A growing number of patients undergoing percutaneous coronary intervention (PCI) with stent implantation also have atrial fibrillation. This poses challenges for their optimal antithrombotic management because patients with atrial fibrillation undergoing PCI require oral anticoagulation for the prevention of cardiac thromboembolism and dual antiplatelet therapy for the prevention of coronary thrombotic complications. The combination of oral anticoagulation and dual antiplatelet therapy substantially increases the risk of bleeding. Over the last decade, a series of North American Consensus Statements on the Management of Antithrombotic Therapy in Patients with Atrial Fibrillation Undergoing Percutaneous Coronary Intervention have been reported. Since the last update in 2018, several pivotal clinical trials in the field have been published. This document provides a focused updated of the 2018 recommendations. The group recommends that in patients with atrial fibrillation undergoing PCI, a non-vitamin K antagonist oral anticoagulant is the oral anticoagulation of choice. Dual antiplatelet therapy with aspirin and a P2Y

Identifiants

pubmed: 33555916
doi: 10.1161/CIRCULATIONAHA.120.050438
doi:

Substances chimiques

Anticoagulants 0
Fibrinolytic Agents 0

Types de publication

Historical Article Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

583-596

Subventions

Organisme : CIHR
Pays : Canada

Auteurs

Dominick J Angiolillo (DJ)

Division of Cardiology, University of Florida College of Medicine, Jacksonville (D.J.A.).

Deepak L Bhatt (DL)

Brigham and Women's Hospital Heart & Vascular Center and Harvard Medical School, Boston, MA (D.L.B., C.P.C., D.P.F.).

Christopher P Cannon (CP)

Brigham and Women's Hospital Heart & Vascular Center and Harvard Medical School, Boston, MA (D.L.B., C.P.C., D.P.F.).

John W Eikelboom (JW)

Department of Medicine, Population Health Research Institute, Thrombosis & Atherosclerosis Research Institute, Hamilton, Canada (J.W.E.).

C Michael Gibson (CM)

Division of Cardiology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA (C.M.G.).

Shaun G Goodman (SG)

St Michael's Hospital, University of Toronto, Canada (S.G.G.).
The Canadian Heart Research Centre, Toronto, Canada (S.G.G.).
Canadian VIGOUR Centre, University of Alberta, Edmonton, Canada (S.G.G.).

Christopher B Granger (CB)

Duke Clinical Research Institute, Duke University, Durham, NC (C.B.G., R.D.L.).

David R Holmes (DR)

Division of Cardiology, Mayo Clinic, Rochester, MN (D.R.H.).

Renato D Lopes (RD)

Duke Clinical Research Institute, Duke University, Durham, NC (C.B.G., R.D.L.).

Roxana Mehran (R)

The Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York (R.M.).

David J Moliterno (DJ)

Division of Cardiovascular Medicine and Gill Heart Institute, University of Kentucky, Lexington (D.J.M.).

Matthew J Price (MJ)

Division of Cardiovascular Diseases, Scripps Clinic, La Jolla, CA (M.J.P.).

Jacqueline Saw (J)

Division of Cardiology, Vancouver General Hospital, University of British Columbia, Canada (J.S.).

Jean-Francois Tanguay (JF)

Department of Medicine, Montreal Heart Institute, Université de Montréal, Canada (J.-F.T.).

David P Faxon (DP)

Brigham and Women's Hospital Heart & Vascular Center and Harvard Medical School, Boston, MA (D.L.B., C.P.C., D.P.F.).

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