Presence of transthyretin amyloidosis cardiomyopathy influences the prognosis of patients with acute decompensated heart failure undergoing cardiac rehabilitation
- PMID: 40895761
- PMCID: PMC12399303
- DOI: 10.1589/jpts.37.444
Presence of transthyretin amyloidosis cardiomyopathy influences the prognosis of patients with acute decompensated heart failure undergoing cardiac rehabilitation
Abstract
[Purpose] This study aimed to investigate the changes in physical function during hospitalization and their impact on the outcomes of patients with transthyretin amyloidosis cardiomyopathy who experienced acute decompensated heart failure and underwent acute cardiac rehabilitation. [Participants and Methods] A matched cohort of 18 and 54 patients with and without transthyretin amyloidosis cardiomyopathy, respectively, was created and analyzed. [Results] Compared to patients without transthyretin amyloidosis cardiomyopathy, those with transthyretin amyloidosis showed similar improvements in grip strength, quadriceps isometric strength, short physical performance battery, and usual gait speed during hospitalization. However, transthyretin amyloidosis cardiomyopathy was associated with a significantly increased risk of both rehospitalization due to heart failure and all-cause mortality. [Conclusion] Although the extent of changes in physical function during hospitalization was similar in patients with and without transthyretin amyloidosis cardiomyopathy, transthyretin amyloidosis cardiomyopathy was associated with poorer outcomes.
Keywords: All-cause mortality; Physical function; Rehospitalization due to heart failure.
2025©by the Society of Physical Therapy Science. Published by IPEC Inc.
Conflict of interest statement
The authors certify that there is no conflict of interest with any financial organization regarding the material discussed in the manuscript.
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