Multimodality imaging approach to cardiac amyloidosis: part 2.

Heart Fail Rev

Heart and Vascular Institute, Henry Ford West Bloomfield Hospital, West Bloomfield, MI, 48322, USA.

Published: September 2022

AI Article Synopsis

  • Recent advancements in cardiac imaging and genetics have led to a better understanding of cardiac amyloidosis (CA), a condition increasingly linked to heart issues like heart failure with preserved ejection fraction (HFPEF).
  • The review emphasizes the combined use of traditional imaging techniques (like ECG and echocardiography) with advanced imaging methods (such as cardiac magnetic resonance and nuclear scintigraphy) in diagnosing and managing CA.
  • An integrated algorithm is proposed for approaching CA, combining clinical assessment, lab tests, and imaging results to improve diagnosis and treatment strategies.

Article Abstract

With recent advances in cardiac imaging, genetics, and treatment options, cardiac amyloidosis (CA) is now recognized as an important and under diagnosed condition contributing to cardiovascular morbidity and mortality. Although still considered a rare disease, CA is now recognized as an important contributor to heart failure with preserved ejection fraction (HFPEF) and low gradient aortic stenosis, two important conditions commonly faced in clinical practice. This review uses clinical scenarios to highlight the complementary role of traditional imaging tools such as electrocardiogram (ECG) and echocardiography (echo) in conjunction with advanced cardiac imaging with cardiac magnetic resonance (CMR) and nuclear cardiac scintigraphy using bone avid tracers in the comprehensive workup of CA. We also highlight the importance of workup of light chain disease as part of integration of imaging findings and discuss the key aspects of various imaging modalities. Finally, an algorithm integrating clinical suspicion, laboratory testing, and imaging in the workup of CA is presented.

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Source
http://dx.doi.org/10.1007/s10741-021-10179-6DOI Listing

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