This Plain Language Summary of Publication article (PLSP) from Future Cardiology examined patients with transthyretin amyloid cardiomyopathy (ATTR-CM). Researchers compared survival rates between patients who received tafamidis treatment and those who didn’t, specifically looking at survival outcomes at 2.5 and 3.5 years. The study also documented side effects experienced by patients taking tafamidis as part of their treatment regimen.

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This PLSP is based on an article called ‘Survival in a Real-World Cohort of Patients With Transthyretin Amyloid Cardiomyopathy Treated With Tafamidis: An Analysis From the Transthyretin Amyloidosis Outcomes Survey (THAOS)’ and was published in the Journal of Cardiac Failure.

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