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JAAPA ; 35(7): 35-39, 2022 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-35762954

RESUMO

ABSTRACT: Cardiac amyloidosis is a rare disorder with a poor long-term prognosis. Presenting features often mirror those of more commonly encountered diseases, making diagnosis challenging. Clinicians should suspect amyloidosis in patients presenting with symptoms of heart failure and preserved ejection fraction. Diagnostic testing assesses for characteristic ECG, echocardiogram, and cardiovascular MRI findings. Confirmatory testing traditionally is performed with endomyocardial biopsy, but safer, less-invasive options exist. Although overall prognosis is unfavorable, contemporary advances in treatment options have improved short-term patient survival.


Assuntos
Injúria Renal Aguda , Amiloidose , Cardiomiopatias , Insuficiência Cardíaca , Injúria Renal Aguda/etiologia , Amiloidose/diagnóstico , Cardiomiopatias/diagnóstico , Insuficiência Cardíaca/diagnóstico por imagem , Insuficiência Cardíaca/terapia , Humanos , Sistemas Automatizados de Assistência Junto ao Leito
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