Diagnosing Transthyretin Cardiac Amyloidosis by Technetium Tc 99m Pyrophosphate: A Test in Evolution.
Publication/Presentation Date
6-1-2021
Abstract
OBJECTIVES: This study aimed to characterize trends in technetium Tc 99m pyrophosphate (
BACKGROUND:
METHODS: Patients undergoing
RESULTS: Over the decade, endomyocardial biopsy rates remained stable with scanning rates peaking at 132 in 2019 (p < 0.001). Among 753 patients (516 men, mean age 77 years), 307 (41%) had a visual score of 0, 177 (23%) of 1, and 269 (36%) of 2 or 3. Of 751 patients with analyzable heart to contralateral chest ratios, 249 (33%) had a ratio ≥1.5. Monoclonal protein testing status was assessed in 550 patients, of these, 174 (32%) did not undergo both serum immunofixation and serum free light chain analysis tests, and 331 (60%) did not undergo all 3 tests-serum immunofixation, serum free light chain analysis, and urine protein electrophoresis. Of 196 patients with confirmed ATTR-CA, 143 (73%) had genetic testing for transthyretin mutations. In 103 patients undergoing cardiac biopsy, grades 2 and 3 99mTc-PYP had sensitivity of 94% and specificity of 89% for ATTR-CA with 100% specificity for grade 3 scans. With respect to SPECT as a reference standard, planar imaging had false positive results in 16 of 25 (64%) grade 2 scans.
CONCLUSIONS: Use of noninvasive testing with
Volume
14
Issue
6
First Page
1221
Last Page
1231
ISSN
1876-7591
Published In/Presented At
Poterucha, Timothy J et al. “Diagnosing Transthyretin Cardiac Amyloidosis by Technetium Tc 99m Pyrophosphate: A Test in Evolution.” JACC. Cardiovascular imaging vol. 14,6 (2021): 1221-1231. doi:10.1016/j.jcmg.2020.08.027
Disciplines
Medicine and Health Sciences
PubMedID
33221204
Department(s)
Department of Medicine
Document Type
Article