Key result
Intensified tafamidis to plus heart failure medications stabilizes symptoms and imaging in ATTR case.
Why the study?
Early detection and individualized management of transthyretin amyloidosis cardiomyopathy require multimodality imaging to guide treatment decisions.
Case Report (n=1)
Answers are grounded in this paper and cite their sources.
Multimodality imaging is crucial for the early detection, monitoring, and individualized management of variant ATTR cardiomyopathy.
Background/Objectives: A 43-year-old male presented with neurological symptoms and asymptomatic cardiac dysfunction, left ventricular hypertrophy, and impaired global longitudinal strain with apical sparing, associated with elevated NT-proBNP. Methods: Multimodality imaging (bone scintigraphy and cardiac magnetic resonance) revealed cardiac amyloid deposition. Genetic testing confirmed variant transthyretin amyloidosis (ATTR) with mixed phenotype. Results: Treatment with tafamidis 20 mg for stage I polyneuropathy, available at that moment, was initiated with good neurological outcome. Three years later, cardiac function deteriorated, following a moderate COVID-19 infection, with heart failure symptoms and reduced ventricular and atrial functions. For progressive ATTR cardiomyopathy, we intensified therapy to tafamidis free acid 61 mg, associated with SGLT2 inhibitor, spironolactone, and furosemide with subsequent improvements of symptoms and stabilization of imaging findings. Conclusions: This case emphasizes the importance of multimodal imaging in early detection, monitoring, and guiding individualized management in ATTR cardiomyopathy.
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Balinisteanu et al. (2025) conducted a case report in Transthyretin amyloidosis (ATTR) (n=1). Tafamidis was evaluated on Clinical and imaging outcomes. Treatment with tafamidis, intensified from to alongside heart failure medications, led to symptom improvement and stabilization of imaging findings in a 43-year-old male with ATTR.
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