A retrospective US analysis found AI-ECG and AI-Echo identified probable ATTR-CM in adults aged 50–95, with dual-positive screens associated with higher mortality.
A retrospective study of 164 patients receiving disease-modifying therapy for ATTR-CM found genetic testing declined with age; 27.3% of tested patients had pathogenic TTR variants.
An LLM chart-review study of 24,080 adults identified 218 untreated patients with suspected ATTR-CA and incomplete evaluations, most lacking a PYP order.
Recent US claims data offer insight into how transthyretin amyloid cardiomyopathy’s diagnosed incidence, prevalence, and associated clinical burden have changed over time.
In this video, Rachel Lampert, MD, Robert W. Berliner Professor of Internal Medicine at the Yale School of Medicine, reviews her presentation at the American College of Cardiology 2025 Annual Meeting,...