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Development and Initial Results from the Canadian Cardiac Amyloidosis Pyrophosphate Imaging Registry (CAPER)
Cigdem Akincioglu1, Natasha Aleksova2, Nowell Fine3
1University of Western Ontario, Medical Imaging, Division of Nuclear Medicine, London, Ontario, Canada.
Transthyretin cardiac amyloidosis (ATTR-CM) diagnosis is improving with Technetium-99m pyrophosphate (PYP) imaging. A Canadian registry shows ATTR-CM prevalence and evaluates diagnostic scoring accuracy.
Area of Science:
- Cardiology
- Nuclear Medicine
- Medical Imaging
Background:
- Transthyretin cardiac amyloidosis (ATTR-CM) is a growing cause of heart failure in elderly individuals.
- Technetium-99m pyrophosphate (PYP) imaging is a key diagnostic tool for ATTR-CM.
- A multicenter Canadian registry was created to study ATTR-CM prevalence and diagnostic accuracy.
Purpose of the Study:
- To establish a multicenter Canadian registry for ATTR-CM research.
- To collect clinical and imaging data for patients undergoing PYP scans.
- To evaluate the accuracy of different risk scores for ATTR-CM diagnosis.
Main Methods:
- Included 2,118 patients from 4 Canadian centers undergoing [99mTc]PYP imaging.
- Collected medical history, cardiac amyloidosis red flags, and laboratory biomarkers.
- Established ATTR-CM diagnosis using standardized criteria and transferred deidentified data.
Main Results:
- ATTR-CM was diagnosed in 29.2% of patients (618/2118), with light chain amyloidosis in 5.3% (112/2118).
- The volume of [99mTc]PYP scans increased significantly from 2016 to 2022.
- The Davies et al. risk score demonstrated higher accuracy for ATTR-CM diagnosis compared to the Nitsche et al. score.
Conclusions:
- A large cohort of patients with detailed clinical and imaging data was assembled.
- The registry provides a valuable resource for ATTR-CM diagnosis and management research.
- The registry is continuously growing, promising future insights into ATTR-CM.
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