What You Need to Know about Undiagnosed Atrial Fibrillation, an Under-Recognized Stroke Risk Factor
- CME / AMA PRA Category 1 Credit™
- MOC / ABIM MOC Part 2 Credit
PROGRAM OVERVIEW
While early diagnosis of atrial fibrillation (AFib) can prevent cardiovascular complications, detecting it can be very challenging. Because stroke risk-assessment scores are seldom calculated in real-world settings, clinicians are often unfamiliar with their use or have insufficient time to determine a patient’s score. Nearly 30% of patients with a CHADS2 score of 3 or greater, but no diagnosed AFib, were later found to experience AFib episodes. Routine electrocardiogram (ECG) screening can help diagnose AFib, but such screening won’t detect sporadic and infrequent events that are often silent or asymptomatic. Various ECG self-monitoring apps have been shown to increase the yield of AFib detection.
This activity will improve the early detection of AFib through use of stroke risk-assessment scores and appropriate long-term monitoring via ECG apps. Participants will also explore the possibilities for oral anticoagulation in patients with diagnosed AFib or high-risk scores.
AGENDA
Welcome, Introduction, Pre‐Survey
The Challenge of Undiagnosed Atrial Fibrillation (AFib)
Approaches to Identify Those at Risk for New AFib
New Approaches for Early AFib Detection
Utility of Screening and Self‐monitoring Detection
Oral Anticoagulation in Newly Identified High‐risk AFib
Q&A Session and Concluding Remarks
TARGET AUDIENCE
This activity is intended for primary care clinicians and other healthcare professionals who treat patients with stroke-associated risk factors and those who may also have atrial fibrillation (AFib).
EDUCATIONAL OBJECTIVES
After completing this activity, the participant should be better able to:
- Identify patients who have high stroke-associated risk using novel approaches for monitoring and diagnosis
- Use the CHA2DS2-VASc risk assessment score as a tool to determine the appropriate course of action to manage diagnosed AFib
- Consider appropriate oral anticoagulation for patients with newly diagnosed AFib and various degrees of disease burden/stroke risk
ACCREDITATION
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 the Potomac Center for Medical Education (PCME) and Rockpointe. The Potomac Center for Medical Education is accredited by the ACCME to provide continuing medical education for physicians.
The Potomac Center for Medical Education designates this enduring material for a maximum of 1.25 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
All other healthcare professionals will be issued a certificate of participation.
CREDIT DESIGNATION
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 the Potomac Center for Medical Education (PCME) and Rockpointe. The Potomac Center for Medical Education is accredited by the ACCME to provide continuing medical education for physicians.
The Potomac Center for Medical Education designates this enduring material for a maximum of 1.25 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
All other healthcare professionals will be issued a certificate of participation.
AMERICAN ACADEMY OF FAMILY PHYSICIANS (AAFP)
This Enduring Material activity, What You Need to Know About Undiagnosed Atrial Fibrillation, An Under-Recognized Stroke Risk Factor, has been reviewed and is acceptable for up to 1.25 Prescribed credit(s) by the American Academy of Family Physicians. AAFP certification begins 11/30/2018. Term of approval is for one year from this date. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
FACULTY

Distinguished Clinical and Research Physician
Intermountain Medical Center Heart Institute
Professor of Medicine
University of Utah
Salt Lake City, UT
He served as recent past Chair of the Task Force on Practice Guidelines for the AHA/ACC and is Past President of the Western States Affiliate of the AHA. He has served as a member and Chair of the FDA’s Cardiorenal Advisory Committee. He is board-certified in cardiovascular diseases and clinical electrophysiology and has a broad interest in cardiovascular diseases and prevention. With his colleagues, he has published more than 700 peer-reviewed and invited articles and book chapters and more than 600 abstracts presented at national and international meetings. His current research interests include cardiovascular genetics, pharmacogenetics, metabolomics and other cardiovascular risk factors, and clinical intervention trials to reduce and prevent cardiovascular diseases. He enjoys seeing and caring for patients, performing innovative clinical research, and teaching at all levels.

Cardiovascular Division
Brigham and Women's Hospital
Professor of Medicine
Harvard Medical School
Boston, MA
Dr. Cannon has published more than 1,000 original articles, reviews, or electronic publications in the field of acute coronary syndromes and prevention and has authored or edited 18 books. He has received numerous awards, including leadership awards from the American College of Cardiology and the American Heart Association.
He has been Principal Investigator of more than 20 multicenter clinical trials, including TACTICS-TIMI 18, PROVE IT, IMPROVE IT, and RE-DUAL PCI trials. Dr. Cannon serves as Executive Director of Cardiometabolic Trials at the Baim Institute for Clinical Research. He is involved in many other trials and registry projects in the fields of acute coronary syndromes, atrial fibrillation, diabetes, lipids, and prevention.

Professor of Medicine
Director, Cardiac Intensive Care Unit
Duke University Medical Center
Durham, NC
Dr. Granger’s primary research interest is in the conduct and methodology of large randomized clinical trials in heart disease; he has co-authored more than 500 peer-reviewed manuscripts. He currently serves on a number of clinical-trial steering committees and data safety monitoring committees. He has coordinated the Duke Clinical Research Institutes’ activities in many clinical trials evaluating acute MI reperfusion and antithrombotic strategies in acute coronary syndromes and atrial fibrillation.
Dr. Granger is Co-chairman of the Steering Committee of the ARISTOTLE trial assessing an oral factor Xa inhibitor for stroke prevention in atrial fibrillation. In addition, he is Co-director of the Reperfusion of Acute MI in Carolina Emergency Departments (RACE) projects, North Carolina state-wide programs to improve reperfusion care for acute myocardial infarction and cardiac arrest.
FACULTY AND PLANNING COMMITTEE DISCLOSURES
Christopher Cannon, MD: Consultant/Independent Contractor: Alnylam, Amarin, Amgen, Arisaph, AstraZeneca, Boehringer Ingelheim, Bristol-Myers Squibb, Eisai, GlaxoSmithKline, Kowa, Lipimedix, Merck, Pfizer, Regeneron, Sanofi, Takeda; Research/Grant Support: Amgen, Arisaph, Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi-Sankyo, Janssen, Merck, Takeda
Christopher B. Granger, MD, FAHA, FACC: Consultant/Independent Contractor: AbbVie, Armetheon, AstraZeneca, Bayer, Boehringer Ingelheim, Boston Scientific, Bristol-Myers Squibb, Daiichi-Sankyo, Gilead Sciences, GlaxoSmithKline, Janssen, Medtronic, Merck, Novartis, Pfizer, Rho Pharmaceuticals, Sirtex, Verseon; Research/Grant Support: Armetheon, AstraZeneca, Bayer, Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi-Sankyo, GlaxoSmithKline, Janssen, Medtronic Foundation, Novartis, Pfizer
Planning and Reviewer Committee: Barry Watkins, PhD, Chad Williamson, MS, MBA, CHCP, Blair St. Amand, Lindsay Scott, PT, DPT, ATC, and Ashley Marostica, RN, MSN, CCM, have no relevant financial relationships to disclose.
Brian W. Jack, AAFP Reviewer: Consultant/Independent Contractor: TeleHealth
FDA DISCLOSURE
SYSTEM REQUIREMENTS
METHOD OF PARTICIPATION
POST-TEST AND EVALUATION
PROVIDER
Jointly provided by the Potomac Center for Medical Education and Rockpointe
SUPPORTER
Supported by an educational grant from the Bristol-Myers Squibb and Pfizer Alliance
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