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December 7, 2019European Heart Journal180 citations

Echocardiographic phenotype and prognosis in transthyretin cardiac amyloidosis

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LCLiza ChackoRMRaffaele MartoneFBFrancesco Bandera

Structured PICO

P
Population
Patients with transthyretin cardiac amyloidosis
O
Outcome
Mortalityhard clinical

Echocardiographic assessment of systolic and diastolic function, along with the presence of severe aortic stenosis, provides important prognostic information regarding survival in transthyretin cardiac amyloidosis.

Abstract

The three distinct genotypes present with varying degrees of severity. Echocardiography indicates a complex pathophysiology in which both systolic and diastolic function are independently associated with mortality. The presence of severe AS was independently associated with significantly reduced patient survival.

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Chacko et al. (2019) studied this question.

synapsesocial.com/papers/69aea782e8b2090a71ff9e76https://doi.org/10.1093/eurheartj/ehz905
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