This CME program, derived from content presented at the European Association of Cardiovascular Imaging Annual Congress EACVI 2023 in Barcelona, Spain, will highlight how to optimize echocardiographic and CMR assessment in the diagnosis and management of hypertrophic cardiomyopathy. In hypertrophic cardiomyopathy, multimodality imaging is crucial to confirm diagnosis, assess for presence and mechanism of left ventricular outflow tract obstruction, and risk stratification for sudden cardiac death. Comfort with echocardiographic techniques to optimize visualization and with cardiac MRI as indicated and as available is required to make best utilization of new therapies for HCM. Our expert faculty will review both research-oriented and practice-pertinent information on the best use of imaging in the contemporary diagnosis and management of HCM.
Healthcare providers across the cardiac care spectrum who perform, interpret, and/or operationalize into the clinical context the results of cardiac imaging studies in patients with or at risk for HCM. This includes cardiologists, interventional cardiologists, electrophysiologists, cardiac surgeons, and other HCPs worldwide, as exemplified by those HCPs attending the EACVI2023 Annual Congress.
Deeper familiarity and comfort with the clinical interpretation of appropriately performed cardiac imaging studies (echocardiography and CMR) in patients with or at risk for HCM
An improved understanding of the prevalence, pathophysiology, unmet patient needs, and natural course of HCM
Operational confidence in recognizing the indications to treat, longitudinally manage, and/or refer to subspecialists, patients diagnosed with HCM
Awareness and understanding of the clinical trial data evaluating the efficacy and safety of new and emerging treatment options for HCM
Echocardiographic Techniques and Tips to Optimize the Diagnosis and Characterization of HCM
When and how to use CMR in the Diagnosis and Characterization of HCM
New and Emerging Treatment Options for HCM
Imaging Case Studies
It is the policy of AcademicCME that all faculty, instructors, and planners disclose relevant financial relationships relating to the topics of this educational activity. Any relevant financial relationships are mitigated via a content review by planning committee members and faculty with no relevant financial relationships.
The faculty reported the following financial relationships or relationships to products or devices they or their spouse/life partner have with commercial interests related to the content of this CE activity:
Faculty | Relationship Identified With: |
Thor Edvardsen, MD, PhD | Nothing to disclose |
Denisa Muraru, MD, PhD | Speaker: GE HealthCare; Philips Medical Systems |
L. Elif Sade, MD | Nothing to disclose |
Timothy Hayes, MD, PhD; Kim Cheramie, MSN, RN-BC; Chelsey Simonds and Nicole McMenamin hereby state that they or their spouse/life partner do not have any relevant financial relationships to products or devices with any commercial interests related to the content of this activity of any amount during the past 12 months.
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AcademicCME designates this enduring material for a maximum of 1.0 AMA PRA Category 1 Credit TM.
Clinicians should claim only the credit commensurate with the extent of their participation in the activity.
This activity has been supported by an independent educational grant from Bristol Myers Squibb.
This educational activity may contain discussion of published and/or investigational uses of agents that are not indicated by the FDA. AcademicCME and Bristol Myers Squibb do not recommend the use of any agent outside of the labeled indications.
Participants have an implied responsibility to use the newly acquired information to enhance patient outcomes and their own professional development. The information presented in this activity is not meant to serve as a guideline for patient management. Any procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this activity should not be used by clinicians without evaluation of their patient’s conditions and possible contraindications on dangers in use, review of any applicable manufacturer’s product information, and comparison with recommendations of other authorities.
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