Key result
Tafamidis significantly reduced the annual rate of cardiovascular-related hospitalizations by 32.4% (RR 0.68) and shortened the mean length of stay compared to placebo in patients with transthyretin amyloid cardiomyopathy.
Why the study?
Because length of stay affects total hospitalization burden, this study evaluated the impact of tafamidis on the number of cardiovascular-related hospital days avoided in patients with ATTR-CM.
Does tafamidis reduce the total number of cardiovascular-related hospitalization days in patients with transthyretin amyloid cardiomyopathy?
Population
Patients with ATTR-CM from ATTR-ACT
Comparison
Tafamidis vs placebo
Design
Post hoc analysis of a clinical trial
Authors
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Tafamidis-associated shorter stays may ease ATTR-CM hospitalization burden; leaves open real-world confirmation beyond trial data.
RCT (n=441)
Randomized
Yes
Does tafamidis reduce the total number of cardiovascular-related hospitalization days in patients with transthyretin amyloid cardiomyopathy?
Relative Risk: 0.68
Absolute Event Rate: 0.475% vs 0.7025%
p-value: p=<0.0001
Tafamidis significantly reduces the frequency and length of cardiovascular-related hospitalizations in patients with ATTR-CM, particularly when initiated early in the disease course.
Rozenbaum et al. (2022) conducted an RCT in Transthyretin Amyloid Cardiomyopathy (n=441). Tafamidis vs. Placebo was evaluated on Mean annual frequency of cardiovascular-related hospitalizations (RRR 0.68, p=<0.0001). Tafamidis significantly reduced the annual rate of cardiovascular-related hospitalizations by 32.4% (RR 0.68) and shortened the mean length of stay compared to placebo in patients with transthyretin amyloid cardiomyopathy.
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