Optimizing Antithrombotic Therapy in Patients With Atrial Fibrillation Who Have an Acute Coronary Syndrome or Have Undergone PCI: New Data, New Directions
 
Release Date: December 18, 2019
Last Reviewed: December 17, 2019
Expiration Date: December 18, 2020
Time to Complete Activity: 1.5 hours

*This activity expired for credit on December 18, 2020 and is no longer available for credit

This activity is jointly provided by Paradigm Medical Communications, LLC and Educational Review Systems, Inc.
       
 
Faculty
Renato D. Lopes, MD, MHS, PhD (Chair)
Professor of Medicine
Division of Cardiology
Duke University Medical Center
Duke Clinical Research Institute
Durham, NC
 
Deepak L. Bhatt, MD, MPH
Professor of Medicine
Harvard Medical School
Executive Director of Interventional Cardiovascular Programs
Division of Cardiovascular Medicine
Brigham and Women’s Hospital
Boston, MA
 
John Fanikos, RPh, MBA
Executive Director of Pharmacy Services
Brigham and Women’s Hospital
Adjunct Professor of Clinical Pharmacy
Massachusetts College of Pharmacy and Health Sciences
Boston, MA
 
Target Audience
This activity has been designed to address the educational needs of general cardiologists, interventional cardiologists, internists, and pharmacists. It may also benefit other healthcare providers (HCPs) who are involved in antithrombotic decisions for patients with atrial fibrillation (AF) who have an acute coronary syndrome (ACS) or have undergone percutaneous coronary intervention (PCI).
 
Statement of Need
Optimal antithrombotic management of patients with AF who have an ACS or have undergone PCI has long been a gray area. In the absence of evidence, clinicians have typically managed such patients with a course of triple therapy—dual antiplatelet therapy (P2Y12 inhibitor + aspirin) plus a vitamin K antagonist (VKA)—to protect against ischemic/thromboembolic events. However, this comes at the cost of higher bleeding risk. Recent data demonstrating significantly safer outcomes with double therapy (P2Y12 inhibitor + non-VKA oral anticoagulant [NOAC]) challenge this long-held standard of care. To upend suboptimal practices, clinicians would benefit from expert-led, case-based education to become familiar with the robust data that herald a new, evidence-based standard of care. Expert guidance on the selection of an oral anticoagulant (OAC) and a P2Y12 inhibitor and the appropriate duration of antiplatelet therapy would help clinicians improve outcomes in the heterogeneous patients with AF who have an ACS or have undergone PCI whom they encounter every day.
 
Learning Objectives
Upon proper completion of this activity, participants should be better able to:
• Interpret key clinical findings from recent trials related to antithrombotic management of patients with AF who have an ACS or have undergone PCI
• Choose optimal antithrombotic treatment for patients with AF who have an ACS or have undergone PCI based on the latest evidence, and with consideration of stroke and bleeding risks
• Individualize the duration of antithrombotic therapy in patients with AF who have an ACS or have undergone PCI based on patient risk factors
 
Table of Contents
• Introduction
• Double Versus Triple Antithrombotic Therapy for Patients With AF Who Have an ACS or Have Undergone PCI: What Does the Evidence Say?
• Case Studies
o Management of Patients With AF Who Have an ACS or Have Undergone PCI: Evidence in Action
 
Physician Accreditation Statement
This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of Paradigm Medical Communications, LLC and Educational Review Systems, Inc. Paradigm Medical Communications, LLC is accredited by the ACCME to provide continuing medical education for physicians.
 
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Paradigm Medical Communications, LLC designates this enduring material for a maximum of 1.5 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
 
Pharmacist Accreditation and Designation Statement
Educational Review Systems is accredited by the Accreditation Council for Pharmacy Education (ACPE) as a provider of continuing pharmacy education. This program is approved for 1.5 hours (0.15 CEUs) of continuing pharmacy education credit. Proof of participation will be posted to your NABP CPE profile within 4 to 6 weeks to participants who have successfully completed the post-test. Participants must participate in the entire presentation and complete the course evaluation to receive continuing pharmacy education credit. (Universal Activity Number – 0761-9999-19-234-H01-P)
 
This is a knowledge-based activity.
 
This activity is jointly provided by Educational Review Systems, Inc and Paradigm Medical Communications, LLC. 
                                                                                     
 
PA Continuing Education
PAs may claim a maximum of 1.5 Category 1 credits for completing this activity. NCCPA accepts AMA PRA Category 1 Credit™ from organizations accredited by ACCME or a recognized state medical society.
 
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The American Academy of Nurse Practitioners Certification Program (AANPCP) accepts certificates of participation for educational activities certified for AMA PRA Category 1 Credit™ from organizations accredited by the ACCME.  Individuals are responsible for checking with the AANPCP for further guidelines.
 
Disclosure of Commercial Support
Supported by educational grants from the Bristol-Myers Squibb and Pfizer Alliance; and AstraZeneca Pharmaceuticals LP.
 
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To receive credit, you should:
• Follow instructions to register or log in with your professional information and complete the preactivity assessment
• View the online activity in its entirety
• Complete and submit the online posttest and evaluation
A certificate of participation/statement of participation will be available for download/printing immediately following your successful completion of the posttest and evaluation.
 
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Disclosures
In accordance with ACCME and ACPE requirements on disclosure, faculty and contributors are asked to disclose any relationships with commercial interests associated with the area of medicine featured in the activity. These relationships are described below.
 
Faculty
Renato D. Lopes, MD, MHS, PhD
Grant/Research Support: Bristol-Myers Squibb Company; GlaxoSmithKline; Medtronic; Pfizer Inc; sanofi-aventis U.S. LLC
Retained Consultant: Bayer HealthCare; Boehringer Ingelheim Pharmaceuticals, Inc; Bristol-Myers Squibb Company; Daiichi Sankyo, Inc; GlaxoSmithKline; Medtronic; Merck & Co., Inc; Pfizer Inc; Portola Pharmaceuticals, Inc.; sanofi-aventis U.S. LLC
 
Deepak L. Bhatt, MD, MPH

Grant/Research Support: Abbott Laboratories; Afimmune Limited; Amarin Corporation; Amgen Inc; AstraZeneca; Bayer HealthCare; Boehringer Ingelheim Pharmaceuticals, Inc; Bristol-Myers Squibb Company; Chiesi USA, Inc.; CSL Behring; Eisai, Inc; Ethicon, Inc; Ferring Pharmaceuticals; Forest Laboratories, Inc; Idorsia Pharmaceuticals Ltd; Ironwood Pharmaceuticals, Inc; Ischemix; Lilly; Medtronic; PhaseBio Pharmaceuticals, Inc.; Pfizer Inc; Regeneron Pharmaceuticals, Inc; Roche; sanofi-aventis U.S. LLC; Synaptic; The Medicines Company
 
John Fanikos, RPh, MBA
No financial relationships to disclose.
 
Paradigm Medical Communications, LLC staff members have no financial relationships to disclose.
 
Educational Review Systems, Inc staff members have no financial relationships to disclose.
 
Independent peer reviewer has no financial relationships to disclose.
 
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