| Literature DB >> 32498813 |
Mazen Hanna1, Frederick L Ruberg2, Mathew S Maurer3, Angela Dispenzieri4, Sharmila Dorbala5, Rodney H Falk5, James Hoffman6, Wael Jaber7, Prem Soman8, Ronald M Witteles9, Martha Grogan10.
Abstract
Technetium-labeled cardiac scintigraphy (i.e., Tc-PYP scan) has been repurposed for the diagnosis of transthyretin amyloid cardiomyopathy (ATTR-CM). Validated in cohorts of patients with heart failure and echocardiographic and/or cardiac magnetic resonance imaging findings suggestive of cardiac amyloidosis, cardiac scintigraphy can confirm the diagnosis of ATTR-CM only when combined with blood and urine testing to exclude a monoclonal protein. Multisocietal guidelines support the nonbiopsy diagnosis of ATTR-CM using cardiac scintigraphy, yet emphasize its use in the appropriate clinical context and the crucial need to rule out light chain amyloid cardiomyopathy. Although increased awareness of ATTR-CM and the advent of effective therapy have led to rapid adoption of diagnostic scintigraphy, there is heterogeneity in adherence to consensus guidelines. This perspective outlines clinical scenarios wherein findings on technetium-labeled cardiac scintigraphy have been misinterpreted, reviews causes of false-negative and false-positive results, and provides strategies to avoid costly and potentially fatal misdiagnoses.Entities:
Keywords: (99m)Tc-DPD; (99m)Tc-HMDP; (99m)Tc-PYP; Technetium-labeled bone scintigraphy; amyloidosis; cardiomyopathy; diagnostic testing; transthyretin
Year: 2020 PMID: 32498813 DOI: 10.1016/j.jacc.2020.04.022
Source DB: PubMed Journal: J Am Coll Cardiol ISSN: 0735-1097 Impact factor: 24.094