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Closing Knowledge Gaps in Transthyretin Cardiomyopathy (ATTR-CM) - Pathophysiology and Clinical Features of TTR Cardiac Amyloidosis: No Longer a “Rare” Disease and Still Underdiagnosed

Pathophysiology and Clinical Features of TTR Cardiac Amyloidosis: No Longer a “Rare” Disease and Still Underdiagnosed

Closing Knowledge Gaps in Transthyretin Cardiomyopathy (ATTR-CM)

06/09/23 • 30 min

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Health Care Practitioners (HCPs) have a pivotal role in ensuring the right patients get the right treatment. Patients living with ATTR-CM have new treatment options that have recently become available. In order to accurately diagnose and treat symptoms unique to the ATTR-CM patient, HCPs need to be aware of the application of guideline-based systematic, multimodal imaging and clinical diagnostics related to ATTR-CM. This podcast will highlight the latest terminology, treatments and guidelines for this no longer rare disease.

Claim CE and MOC at https://bit.ly/ATTR-CM_series

06/09/23 • 30 min

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