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Curr Probl Cardiol ; 49(3): 102385, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38184135

ABSTRACT

INTRODUCTION: Transthyretin amyloid cardiomyopathy (ATTR-CM) is an underdiagnosed cause of AHF that benefits from a specific approach. The aim was to determine the prevalence of ATTR-CM among patients hospitalized for AHF. METHODS: A prospective study was conducted on consecutive patients aged 60 or older admitted for acute AHF without cardiogenic shock. RESULTS: The study included 103 patients, a total of 16 patients (15.5 %) were compatible with ATTR-CM. The ATTR-CM group showed a higher septal wall thickness (18.1 mm vs. 11.8 mm; P = 0.001), lower systolic excursion of the tricuspid annular plane (15 mm vs. 18.3 mm, P = 0.014), and S wave of the right ventricle (8 cm/s vs. 9.2 cm/s P=0.032). CONCLUSION: ATTR-CM is an underdiagnosed condition, there are some variables associated with its diagnosis. The coexistence with other comorbidities causing AHF, highlights the importance of considering screening for this cardiomyopathy in adults hospitalized for AHF.


Subject(s)
Amyloid Neuropathies, Familial , Cardiomyopathies , Heart Failure , Adult , Humans , Amyloid Neuropathies, Familial/complications , Amyloid Neuropathies, Familial/diagnosis , Amyloid Neuropathies, Familial/epidemiology , Cardiomyopathies/diagnosis , Cardiomyopathies/epidemiology , Cardiomyopathies/complications , Heart Failure/diagnosis , Heart Failure/epidemiology , Heart Failure/complications , Prealbumin , Prevalence , Prospective Studies
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