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. 2021 May 10;11(3):407–412. doi: 10.1080/20009666.2021.1915547

Table 2.

Diagnostic Modalities for AL-type Cardiac Amyloidosis [6,10]

Diagnostic modality Sensitivity, specificity (Percentages) Findings consistent with cardiac amyloid
EKG 90%, 90% Diffuse low voltage QRS (<5 mm height), QRS deviation, LBBBs, pseudo–infarction
Echocardiography with strain imaging 90–95%, 80-85% Biventricular hypertrophy, inter-ventricular septal hypertrophy, bi-atrial dilation, decreased longitudinal strain in mid and basal wall with relative sparing of apical function
Cardiac MRI 80%, 94% Global transmural or subendocardial late gadolinium enhancement, expansion of ECV leading to enhanced T1 mapping
Nuclear Scintigraphy (Positron Emission Tomography – PET, Technetium labelled imaging) 95%, 98% Characteristic enhancement due to binding of radiotracer to amyloid
Histopathology 100% sensitivity for endomyocardial biopsy,
Tissue biopsy has sensitivity of 75% and specificity of 92%
Fat pad biopsy, Endomyocardial biopsy with immunohistochemical staining showing extracellular deposits of AL amyloid with Congo red stain showing apple-green birefringence under polarized microscopy

MRI: Magnetic resonance imaging, LBBB: Left bundle branch block, ECV: Extracellular volume, PET: Positron emission tomography