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Implantation of a left ventricular assist device to provide long‐term support for end‐stage Duchenne muscular dystrophy‐associated cardiomyopathy
A young man with Duchenne muscular dystrophy presented to the UT Southwestern Neuromuscular Cardiomyopathy Clinic with advanced heart failure. Despite maximal medical therapy, his cardiac function continued to decline requiring initiation of inotrope therapy. Given the patient's clinical deteri...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542741/ https://www.ncbi.nlm.nih.gov/pubmed/28772036 http://dx.doi.org/10.1002/ehf2.12160 |
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author | Stoller, Douglas Araj, Faris Amin, Alpesh Fitzsimmons, Catherine Morlend, Robert Thibodeau, Jennifer T. Ramaciotti, Claudio Drazner, Mark H. Meyer, Dan M. Mammen, Pradeep P.A. |
author_facet | Stoller, Douglas Araj, Faris Amin, Alpesh Fitzsimmons, Catherine Morlend, Robert Thibodeau, Jennifer T. Ramaciotti, Claudio Drazner, Mark H. Meyer, Dan M. Mammen, Pradeep P.A. |
author_sort | Stoller, Douglas |
collection | PubMed |
description | A young man with Duchenne muscular dystrophy presented to the UT Southwestern Neuromuscular Cardiomyopathy Clinic with advanced heart failure. Despite maximal medical therapy, his cardiac function continued to decline requiring initiation of inotrope therapy. Given the patient's clinical deterioration, a left ventricular assist device (LVAD) was implanted as destination therapy after undergoing a multidisciplinary assessment. The patient tolerated the surgical implantation of the LVAD without any significant complications, and he has had a relatively unremarkable course 38 months post‐LVAD implantation. A critical factor contributing to the long‐term success of this patient was the decision to select an LVAD that would not disrupt the diaphragm and thus preserve the respiratory muscle strength. This case demonstrates that permanent mechanical LVADs should be considered for appropriately selected Duchenne muscular dystrophy patients with medically refractory end‐stage cardiomyopathy. |
format | Online Article Text |
id | pubmed-5542741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55427412017-08-17 Implantation of a left ventricular assist device to provide long‐term support for end‐stage Duchenne muscular dystrophy‐associated cardiomyopathy Stoller, Douglas Araj, Faris Amin, Alpesh Fitzsimmons, Catherine Morlend, Robert Thibodeau, Jennifer T. Ramaciotti, Claudio Drazner, Mark H. Meyer, Dan M. Mammen, Pradeep P.A. ESC Heart Fail Case Reports A young man with Duchenne muscular dystrophy presented to the UT Southwestern Neuromuscular Cardiomyopathy Clinic with advanced heart failure. Despite maximal medical therapy, his cardiac function continued to decline requiring initiation of inotrope therapy. Given the patient's clinical deterioration, a left ventricular assist device (LVAD) was implanted as destination therapy after undergoing a multidisciplinary assessment. The patient tolerated the surgical implantation of the LVAD without any significant complications, and he has had a relatively unremarkable course 38 months post‐LVAD implantation. A critical factor contributing to the long‐term success of this patient was the decision to select an LVAD that would not disrupt the diaphragm and thus preserve the respiratory muscle strength. This case demonstrates that permanent mechanical LVADs should be considered for appropriately selected Duchenne muscular dystrophy patients with medically refractory end‐stage cardiomyopathy. John Wiley and Sons Inc. 2017-05-11 /pmc/articles/PMC5542741/ /pubmed/28772036 http://dx.doi.org/10.1002/ehf2.12160 Text en © 2017 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Reports Stoller, Douglas Araj, Faris Amin, Alpesh Fitzsimmons, Catherine Morlend, Robert Thibodeau, Jennifer T. Ramaciotti, Claudio Drazner, Mark H. Meyer, Dan M. Mammen, Pradeep P.A. Implantation of a left ventricular assist device to provide long‐term support for end‐stage Duchenne muscular dystrophy‐associated cardiomyopathy |
title | Implantation of a left ventricular assist device to provide long‐term support for end‐stage Duchenne muscular dystrophy‐associated cardiomyopathy |
title_full | Implantation of a left ventricular assist device to provide long‐term support for end‐stage Duchenne muscular dystrophy‐associated cardiomyopathy |
title_fullStr | Implantation of a left ventricular assist device to provide long‐term support for end‐stage Duchenne muscular dystrophy‐associated cardiomyopathy |
title_full_unstemmed | Implantation of a left ventricular assist device to provide long‐term support for end‐stage Duchenne muscular dystrophy‐associated cardiomyopathy |
title_short | Implantation of a left ventricular assist device to provide long‐term support for end‐stage Duchenne muscular dystrophy‐associated cardiomyopathy |
title_sort | implantation of a left ventricular assist device to provide long‐term support for end‐stage duchenne muscular dystrophy‐associated cardiomyopathy |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542741/ https://www.ncbi.nlm.nih.gov/pubmed/28772036 http://dx.doi.org/10.1002/ehf2.12160 |
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