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Surgical repair for common arterial trunk with pulmonary dominance, hypoplasia of ascending aorta, and interrupted aortic arch

The arrangement of aortic and pulmonary pathways is extremely variable in the hearts with a common arterial trunk. Almost always, interruption of the aortic arch is seen in the setting of hypoplasia of the ascending aorta and dominance of the pulmonary circulation. This subset poses substantial chal...

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Autores principales: Talwar, Sachin, Siddharth, Bharat, Gupta, Saurabh Kumar, Bhoje, Amolkumar, Choudhary, Shiv Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716323/
https://www.ncbi.nlm.nih.gov/pubmed/31516284
http://dx.doi.org/10.4103/apc.APC_147_18
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author Talwar, Sachin
Siddharth, Bharat
Gupta, Saurabh Kumar
Bhoje, Amolkumar
Choudhary, Shiv Kumar
author_facet Talwar, Sachin
Siddharth, Bharat
Gupta, Saurabh Kumar
Bhoje, Amolkumar
Choudhary, Shiv Kumar
author_sort Talwar, Sachin
collection PubMed
description The arrangement of aortic and pulmonary pathways is extremely variable in the hearts with a common arterial trunk. Almost always, interruption of the aortic arch is seen in the setting of hypoplasia of the ascending aorta and dominance of the pulmonary circulation. This subset poses substantial challenges in surgical repair and portends poor outcomes. In this report, we briefly describe the technique of ascending aorta reconstruction and other aspects of the surgical repair of this rare malformation.
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spelling pubmed-67163232019-09-12 Surgical repair for common arterial trunk with pulmonary dominance, hypoplasia of ascending aorta, and interrupted aortic arch Talwar, Sachin Siddharth, Bharat Gupta, Saurabh Kumar Bhoje, Amolkumar Choudhary, Shiv Kumar Ann Pediatr Cardiol Brief Communication The arrangement of aortic and pulmonary pathways is extremely variable in the hearts with a common arterial trunk. Almost always, interruption of the aortic arch is seen in the setting of hypoplasia of the ascending aorta and dominance of the pulmonary circulation. This subset poses substantial challenges in surgical repair and portends poor outcomes. In this report, we briefly describe the technique of ascending aorta reconstruction and other aspects of the surgical repair of this rare malformation. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6716323/ /pubmed/31516284 http://dx.doi.org/10.4103/apc.APC_147_18 Text en Copyright: © 2019 Annals of Pediatric Cardiology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Brief Communication
Talwar, Sachin
Siddharth, Bharat
Gupta, Saurabh Kumar
Bhoje, Amolkumar
Choudhary, Shiv Kumar
Surgical repair for common arterial trunk with pulmonary dominance, hypoplasia of ascending aorta, and interrupted aortic arch
title Surgical repair for common arterial trunk with pulmonary dominance, hypoplasia of ascending aorta, and interrupted aortic arch
title_full Surgical repair for common arterial trunk with pulmonary dominance, hypoplasia of ascending aorta, and interrupted aortic arch
title_fullStr Surgical repair for common arterial trunk with pulmonary dominance, hypoplasia of ascending aorta, and interrupted aortic arch
title_full_unstemmed Surgical repair for common arterial trunk with pulmonary dominance, hypoplasia of ascending aorta, and interrupted aortic arch
title_short Surgical repair for common arterial trunk with pulmonary dominance, hypoplasia of ascending aorta, and interrupted aortic arch
title_sort surgical repair for common arterial trunk with pulmonary dominance, hypoplasia of ascending aorta, and interrupted aortic arch
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716323/
https://www.ncbi.nlm.nih.gov/pubmed/31516284
http://dx.doi.org/10.4103/apc.APC_147_18
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