Case Presentation of Patients Using the Cardiac Amyloidosis Pathway

  • Batel Nissan*
  • , Mutaz Karameh
  • , David Leibowitz
  • , Eyal Herzog
  • , Arthur Pollak
  • , Elchanan Parnasa
  • , Yonatan Rashi
  • , Karen Meir
  • *Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

Abstract

Our team developed and published in late 2023 a novel and simple pathway to help health care providers diagnose and treat patients with cardiac amyloidosis. In the book of “Cardiac Amyloidosis” we have updated and modified this pathway. The pathway starts with a section titled “suspicion” in which we provide simple clues or “red flags” that are associated with the cardiac amyloidosis phenotype. It is followed by a section titled “diagnosis,” where we present in a simplified 2 × 2 format the laboratory and imaging tests that must be performed for an accurate diagnosis. In the section titled “treatment,” we describe the 4 pillars in the management of patients with cardiac amyloidosis, which include: heart failure treatments, management of arrhythmias, treatment of significant aortic stenosis, and appropriate selection of disease modifying therapies. Our algorithm ends with our simplified recommendation for follow-up. In this chapter we present the same pathway with 14 steps to guide health care providers in managing patients with cardiac amyloidosis. We present 6 cases of patients diagnosed with cardiac amyloidosis. These cases illustrate clinical application of the cardiac amyloidosis pathway, and illustrate the process of suspicion, diagnosis, treatment and follow up of patients with cardiac amyloidosis.

Original languageEnglish
Title of host publicationCardiac Amyloidosis
PublisherSpringer Science+Business Media
Pages325-345
Number of pages21
ISBN (Electronic)9783031883422
ISBN (Print)9783031883415
DOIs
StatePublished - 1 Jan 2025

Bibliographical note

Publisher Copyright:
© 2025 The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerland AG.

Keywords

  • Cardiac amyloidosis
  • Clinical cases
  • Heart failure
  • Pathway
  • Tafamidis
  • Transthyretin protein

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