Live Q&A: HCM Around the Globe: Not an Isolated Issue
Premiere Date: Thursday, June 30, 2022This activity offers CE credit for:
%>- Medicine (accme)
- Nursing (ANCC)
- Pharmacy (acpe)
- PA (aapa)
- Other
All other clinicians will receive a Certificate of Attendance stating this activity was certified for AMA PRA Category 1 Credit™
Credit Expiration Date:
Friday, June 30, 2023
Note: Credit Is No Longer Available
Martin S. Maron, MD (Moderator) Director, Hypertrophic Cardiomyopathy Center Co-Director, Cardiac CT and MRI Assistant Professor Tufts University School of Medicine Boston, MA |
Iacopo Olivotto, MD Professor Head, Cardiomyopathy Unit Careggi University Hospital University of Florence Florence, Italy |
Marco Antonio Rodrigues Torres, MD, PhD Post Graduation Professor Federal University of Rio Grande do Sul (UFRGS) Porto Alegre, Brazil |
Hypertrophic cardiomyopathy (HCM) is the most common inherited monogenic cardiovascular disease, yet it is frequently overlooked as a cause of cardiac symptoms. Key diagnostic strategies include echocardiography and cardiovascular MRI. Evaluating patients with HCM for provocable left ventricular outflow obstruction (LVOT) can help to identify more patients with treatable obstructive disease. Once diagnosed, treatment options include β-adrenergic receptor blockers and calcium channel blockers. Disopyramide can be effective as an add-on therapy but is associated with side effects and contraindications. In experienced centers, septal myectomy or alcohol septal ablation can lead to near-complete resolution of resting and inducible LVOT gradients, but experienced surgeons and specialized centers are limited in many parts of the world. Most recently, a first-in-class oral myosin inhibitor, mavacamten, was approved by the FDA for obstructive HCM, providing a new, non-invasive option for appropriate patients.
In this live Q&A session, three international experts from the CME Outfitters “Snack” series on HCM come together to answer your questions about optimizing the management of HCM, including the role of myosin inhibition.
At the end of this CE activity, participants should be able to:
- Screen appropriate patients for HCM using evidence-based diagnostic strategies.
- Implement global and country-specific practice guideline recommendations to improve care for patients with HCM.
- Assess study results of emerging HCM disease-specific treatments targeting cardiac myosin.
Supported by an educational grant from Bristol Myers Squibb.
Cardiologists, interventional cardiologists, electrophysiologists, cardiac surgeons (Secondary: Primary care physicians/General practitioners, PAs, nurse practitioners, nurses, and pharmacists)
EACCME:
Through a mutual recognition agreement between the AMA and the UEMS-EACCME, European physicians completing an e-learning activity from a US-based ACCME-accredited CME provider can use AMA PRA Category 1 Credit™ toward their credit requirements. CME Outfitters is based in Radnor, Pennsylvania, USA. Please retain your certificate as proof of completion.
Dr. Maron reports the following financial relationships:
Advisory Board: Cytokenetics (REDWOOD-HCM Steering Committee)
Consultant: Imbria and Takeda Pharmaceuticals U.S.A., Inc.
Dr. Olivotto reports the following financial relationships:
Advisory Board: Amicus Therapeutics, Inc.; Bristol Myers Squibb; Cytokinetics; and Tenaya Therapeutics
Consultant: Amicus Therapeutics, Inc.; Bayer; Bristol Myers Squibb; Cytokinetics; Genzyme; and Tenaya Therapeutics
Dr. Torres reports no financial relationships.
The following CME Outfitters staff have no financial relationships:
Faculty of this CE activity may include discussions of products or devices that are not currently labeled for use by the FDA. The faculty have been informed of their responsibility to disclose to the audience if they will be discussing off-label or investigational uses (any uses not approved by the FDA) of products or devices.
Questions about this activity? Call us at 877.CME.PROS (877.263.7767).
SNQ-164-063022-08