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The role of the Fontan operation in the treatment of congenitally corrected transposition of the great arteries
Congenitally corrected transposition of the great arteries (ccTGA) is a complex cardiac anomaly with an unfavorable natural history. Surgical treatment has been available for over 50 years. Initial procedures used for ccTGA did not correct atrio-ventricular discordance, leaving the right ventricle i...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180964/ https://www.ncbi.nlm.nih.gov/pubmed/21976866 http://dx.doi.org/10.4103/0974-2069.84634 |
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author | Karl, Tom R |
author_facet | Karl, Tom R |
author_sort | Karl, Tom R |
collection | PubMed |
description | Congenitally corrected transposition of the great arteries (ccTGA) is a complex cardiac anomaly with an unfavorable natural history. Surgical treatment has been available for over 50 years. Initial procedures used for ccTGA did not correct atrio-ventricular discordance, leaving the right ventricle in systemic position. In the past two decades anatomic repair has been considered to be a better option. Many cases subjected to anatomic repairs would also be suitable for the Fontan strategy, which probably has a lower initial risk. The rationale for use of the Fontan operation in management of congenitally corrected transposition is discussed in this review, with comparisons to other strategies. |
format | Online Article Text |
id | pubmed-3180964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-31809642011-10-04 The role of the Fontan operation in the treatment of congenitally corrected transposition of the great arteries Karl, Tom R Ann Pediatr Cardiol Perspective Congenitally corrected transposition of the great arteries (ccTGA) is a complex cardiac anomaly with an unfavorable natural history. Surgical treatment has been available for over 50 years. Initial procedures used for ccTGA did not correct atrio-ventricular discordance, leaving the right ventricle in systemic position. In the past two decades anatomic repair has been considered to be a better option. Many cases subjected to anatomic repairs would also be suitable for the Fontan strategy, which probably has a lower initial risk. The rationale for use of the Fontan operation in management of congenitally corrected transposition is discussed in this review, with comparisons to other strategies. Medknow Publications 2011 /pmc/articles/PMC3180964/ /pubmed/21976866 http://dx.doi.org/10.4103/0974-2069.84634 Text en © Annals of Pediatric Cardiology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Perspective Karl, Tom R The role of the Fontan operation in the treatment of congenitally corrected transposition of the great arteries |
title | The role of the Fontan operation in the treatment of congenitally corrected transposition of the great arteries |
title_full | The role of the Fontan operation in the treatment of congenitally corrected transposition of the great arteries |
title_fullStr | The role of the Fontan operation in the treatment of congenitally corrected transposition of the great arteries |
title_full_unstemmed | The role of the Fontan operation in the treatment of congenitally corrected transposition of the great arteries |
title_short | The role of the Fontan operation in the treatment of congenitally corrected transposition of the great arteries |
title_sort | role of the fontan operation in the treatment of congenitally corrected transposition of the great arteries |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180964/ https://www.ncbi.nlm.nih.gov/pubmed/21976866 http://dx.doi.org/10.4103/0974-2069.84634 |
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