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Treatment of Transthyretin Cardiac Amyloidosis

Cardiac amyloidosis is increasing in incidence and prevalence, but often remains under-recognized, undetected, and undertreated. These findings suggest that cardiovascular (CV) clinicians are less aware and attentive to the substantial morbidity and mortality associated with the progressive nature of cardiac amyloidosis and treatment for this patient population remains suboptimal. 

Education is needed on recognizing “red flags” and having heightened suspicion to expedite earlier detection, incorporate guideline recommendations for diagnostic algorithms using non-invasive imaging modalities, and gain knowledge on rapidly emerging disease-modifying targeted treatment strategies for cardiac amyloidosis to improve patient outcomes. 


Target Audience: 

CV team clinicians including physicians, nurse practitioners, physician assistants and pharmacists who identify and manage patients with cardiac amyloidosis. 

Important Dates: 
Date of Release: 1/09/2023 
Term of Approval/Date of Expiration: 1/08/2024
Learner Objective:  
Upon completion of this activity, the learner should be able to:

  • Review treatment options for patients diagnosed with cardiac amyloidosis.  

Educational grant support provided by: Alnylam Pharmaceuticals, Inc. 


Richard Kar-Hang Cheng, MD, MSc, FACC  

Disclaimer: This activity does not offer credit. 

Availability: On-Demand
Expires on Jan 08, 2024
Cost: FREE
Credit Offered:
No Credit Offered
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