JACC. CardioOncology (Dec 2019)

Best Practices for Prognostic Evaluation of a Patient With Transthyretin Amyloid Cardiomyopathy

  • Kent Y. Feng, MD,
  • Rahul S. Loungani, MD,
  • Vishal N. Rao, MD, MPH,
  • Chetan B. Patel, MD,
  • Michel G. Khouri, MD,
  • G. Michael Felker, MD, MHS,
  • Adam D. DeVore, MD, MHS

Journal volume & issue
Vol. 1, no. 2
pp. 273 – 279

Abstract

Read online

Transthyretin amyloid cardiomyopathy (ATTR-CM) has emerged as an increasingly identified etiology of heart failure. Fortunately, the disease now has an approved therapy, with many others under development. Assessment of prognosis in ATTR-CM is critical to inform patients about the disease course and guide clinical decisions. This review discusses the evidence behind clinical, biomarker, and imaging findings that inform prognosis in patients with ATTR-CM and can assist providers in the shared decision-making process during management of this disease.

Keywords