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Trasplante cardiaco por amiloidosis. Manifestaciones clínicas e imagenológicas

OBJECTIVE: To describe the clinical and imaging characteristics of heart transplantation patients due to amyloidosis in a community institution. METHOD: Descriptive case series of consecutive heart transplantation patients with amyloidosis in a medical center. All patients with diagnosis of amyloido...

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Autores principales: Decotto, Santiago, Villanueva, Eugenia, de Arenaza, Diego Pérez, Nucifora, Elsa M., Aguirre, María A., Posadas-Martínez, María L., Marenchino, Ricardo G., Belziti, César A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Permanyer Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262297/
https://www.ncbi.nlm.nih.gov/pubmed/34619747
http://dx.doi.org/10.24875/ACM.21000191
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author Decotto, Santiago
Villanueva, Eugenia
de Arenaza, Diego Pérez
Nucifora, Elsa M.
Aguirre, María A.
Posadas-Martínez, María L.
Marenchino, Ricardo G.
Belziti, César A.
author_facet Decotto, Santiago
Villanueva, Eugenia
de Arenaza, Diego Pérez
Nucifora, Elsa M.
Aguirre, María A.
Posadas-Martínez, María L.
Marenchino, Ricardo G.
Belziti, César A.
author_sort Decotto, Santiago
collection PubMed
description OBJECTIVE: To describe the clinical and imaging characteristics of heart transplantation patients due to amyloidosis in a community institution. METHOD: Descriptive case series of consecutive heart transplantation patients with amyloidosis in a medical center. All patients with diagnosis of amyloidosis with cardiac compromise receiving heart transplantation, performed in the period November 2008 to February 2021, were included in the analysis. RESULTS: A total of 16 patients were included. The mean age was 59.9 years (± 10.2). 81.25% (n = 13) were male. According to the type of amyloidosis, 12 patients were transplanted for AL amyloidosis and 4 for ATTR amyloidosis. The most frequent clinical presentations were left overload (50%) and cardiogenic shock (32%). The mean ejection fraction prior to transplantation was 43% (± 16), 14 of the 16 patients had right ventricular dysfunction. The most common finding on cardiac magnetic resonance was the diffuse subendocardial late gadolinium enhancement pattern, with cancellation of the blood pool. The heart transplantation gave 6 patients the chance to receive a bone marrow transplantation afterwards. CONCLUSIONS: Heart transplantation has become an option for patients with heart failure due to AL and ATTR amyloidosis. In patients with AL amyloidosis, it might even allow bone marrow transplantation in a second stage.
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spelling pubmed-92622972022-07-08 Trasplante cardiaco por amiloidosis. Manifestaciones clínicas e imagenológicas Decotto, Santiago Villanueva, Eugenia de Arenaza, Diego Pérez Nucifora, Elsa M. Aguirre, María A. Posadas-Martínez, María L. Marenchino, Ricardo G. Belziti, César A. Arch Cardiol Mex Artículo De Investigación OBJECTIVE: To describe the clinical and imaging characteristics of heart transplantation patients due to amyloidosis in a community institution. METHOD: Descriptive case series of consecutive heart transplantation patients with amyloidosis in a medical center. All patients with diagnosis of amyloidosis with cardiac compromise receiving heart transplantation, performed in the period November 2008 to February 2021, were included in the analysis. RESULTS: A total of 16 patients were included. The mean age was 59.9 years (± 10.2). 81.25% (n = 13) were male. According to the type of amyloidosis, 12 patients were transplanted for AL amyloidosis and 4 for ATTR amyloidosis. The most frequent clinical presentations were left overload (50%) and cardiogenic shock (32%). The mean ejection fraction prior to transplantation was 43% (± 16), 14 of the 16 patients had right ventricular dysfunction. The most common finding on cardiac magnetic resonance was the diffuse subendocardial late gadolinium enhancement pattern, with cancellation of the blood pool. The heart transplantation gave 6 patients the chance to receive a bone marrow transplantation afterwards. CONCLUSIONS: Heart transplantation has become an option for patients with heart failure due to AL and ATTR amyloidosis. In patients with AL amyloidosis, it might even allow bone marrow transplantation in a second stage. Permanyer Publications 2022 2021-10-06 /pmc/articles/PMC9262297/ /pubmed/34619747 http://dx.doi.org/10.24875/ACM.21000191 Text en Copyright: © 2022 Permanyer https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Artículo De Investigación
Decotto, Santiago
Villanueva, Eugenia
de Arenaza, Diego Pérez
Nucifora, Elsa M.
Aguirre, María A.
Posadas-Martínez, María L.
Marenchino, Ricardo G.
Belziti, César A.
Trasplante cardiaco por amiloidosis. Manifestaciones clínicas e imagenológicas
title Trasplante cardiaco por amiloidosis. Manifestaciones clínicas e imagenológicas
title_full Trasplante cardiaco por amiloidosis. Manifestaciones clínicas e imagenológicas
title_fullStr Trasplante cardiaco por amiloidosis. Manifestaciones clínicas e imagenológicas
title_full_unstemmed Trasplante cardiaco por amiloidosis. Manifestaciones clínicas e imagenológicas
title_short Trasplante cardiaco por amiloidosis. Manifestaciones clínicas e imagenológicas
title_sort trasplante cardiaco por amiloidosis. manifestaciones clínicas e imagenológicas
topic Artículo De Investigación
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9262297/
https://www.ncbi.nlm.nih.gov/pubmed/34619747
http://dx.doi.org/10.24875/ACM.21000191
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