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Partially reversible bortezomib-induced cardiotoxicity: an unusual cause of acute cardiomyopathy

Chemotherapy-associated cardiotoxicity can present as a spectrum from arrhythmia to acute congestive heart failure. Unlike anthracyclines, proteasome inhibitors – for example, bortezomib – are not notorious for causing cardiotoxicity in absence of pre-existing cardiac dysfunction or without concomit...

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Autores principales: Meseeha, Marcelle G., Kolade, Victor O., Attia, Maximos N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Co-Action Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677580/
https://www.ncbi.nlm.nih.gov/pubmed/26653686
http://dx.doi.org/10.3402/jchimp.v5.28982
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author Meseeha, Marcelle G.
Kolade, Victor O.
Attia, Maximos N.
author_facet Meseeha, Marcelle G.
Kolade, Victor O.
Attia, Maximos N.
author_sort Meseeha, Marcelle G.
collection PubMed
description Chemotherapy-associated cardiotoxicity can present as a spectrum from arrhythmia to acute congestive heart failure. Unlike anthracyclines, proteasome inhibitors – for example, bortezomib – are not notorious for causing cardiotoxicity in absence of pre-existing cardiac dysfunction or without concomitant use of other cardiotoxic agents. We describe a 66-year-old woman with end-stage renal disease who developed acute dyspnea hours after a third treatment with bortezomib for IgG kappa myeloma. The Naranjo adverse drug reaction probability scale indicated a probable relationship (score of 5) between bortezomib and acute left ventricular dysfunction. Patients receiving proteasome inhibitors should be closely monitored for evidence of cardiac dysfunction during treatment.
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spelling pubmed-46775802016-01-05 Partially reversible bortezomib-induced cardiotoxicity: an unusual cause of acute cardiomyopathy Meseeha, Marcelle G. Kolade, Victor O. Attia, Maximos N. J Community Hosp Intern Med Perspect Case Report Chemotherapy-associated cardiotoxicity can present as a spectrum from arrhythmia to acute congestive heart failure. Unlike anthracyclines, proteasome inhibitors – for example, bortezomib – are not notorious for causing cardiotoxicity in absence of pre-existing cardiac dysfunction or without concomitant use of other cardiotoxic agents. We describe a 66-year-old woman with end-stage renal disease who developed acute dyspnea hours after a third treatment with bortezomib for IgG kappa myeloma. The Naranjo adverse drug reaction probability scale indicated a probable relationship (score of 5) between bortezomib and acute left ventricular dysfunction. Patients receiving proteasome inhibitors should be closely monitored for evidence of cardiac dysfunction during treatment. Co-Action Publishing 2015-12-11 /pmc/articles/PMC4677580/ /pubmed/26653686 http://dx.doi.org/10.3402/jchimp.v5.28982 Text en © 2015 Marcelle G. Meseeha et al. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Meseeha, Marcelle G.
Kolade, Victor O.
Attia, Maximos N.
Partially reversible bortezomib-induced cardiotoxicity: an unusual cause of acute cardiomyopathy
title Partially reversible bortezomib-induced cardiotoxicity: an unusual cause of acute cardiomyopathy
title_full Partially reversible bortezomib-induced cardiotoxicity: an unusual cause of acute cardiomyopathy
title_fullStr Partially reversible bortezomib-induced cardiotoxicity: an unusual cause of acute cardiomyopathy
title_full_unstemmed Partially reversible bortezomib-induced cardiotoxicity: an unusual cause of acute cardiomyopathy
title_short Partially reversible bortezomib-induced cardiotoxicity: an unusual cause of acute cardiomyopathy
title_sort partially reversible bortezomib-induced cardiotoxicity: an unusual cause of acute cardiomyopathy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677580/
https://www.ncbi.nlm.nih.gov/pubmed/26653686
http://dx.doi.org/10.3402/jchimp.v5.28982
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