Coarctation: A Review

Coarctation of the aorta occurs in 0.04% of the population, and accounts for approximately 10% of lesions in adults with congenital heart disease. It can occur as an isolated lesion or as a part of a complex defect, and is most commonly associated with bicuspid aortic valve, ventricular septal defec...

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Autor principal: Marc G Cribbs
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Lenguaje:EN
Publicado: Radcliffe Medical Media 2020
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Acceso en línea:https://doaj.org/article/cbee9634a31d4129b8cc3a3861c983b4
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spelling oai:doaj.org-article:cbee9634a31d4129b8cc3a3861c983b42021-12-04T16:02:21ZCoarctation: A Review10.15420/usc.2019.15.21758-390X1758-3896https://doaj.org/article/cbee9634a31d4129b8cc3a3861c983b42020-02-01T00:00:00Zhttps://www.uscjournal.com/articles/Coarctation-A-Reviewhttps://doaj.org/toc/1758-3896https://doaj.org/toc/1758-390XCoarctation of the aorta occurs in 0.04% of the population, and accounts for approximately 10% of lesions in adults with congenital heart disease. It can occur as an isolated lesion or as a part of a complex defect, and is most commonly associated with bicuspid aortic valve, ventricular septal defect, and mitral valve abnormalities. Since the first surgical repair in 1944, the available treatment options have expanded greatly. Perhaps one of the most important advances in the management of coarctation of the aorta has been the development of transcatheter therapy for both native and especially recurrent coarctation of the aorta. Late complications, even after apparently successful treatment, are not uncommon. For this reason, lifelong follow-up is vital.Marc G CribbsRadcliffe Medical MediaarticleDiseases of the circulatory (Cardiovascular) systemRC666-701ENUS Cardiology Review , Vol 13, Iss 2, Pp 99-104 (2020)
institution DOAJ
collection DOAJ
language EN
topic Diseases of the circulatory (Cardiovascular) system
RC666-701
spellingShingle Diseases of the circulatory (Cardiovascular) system
RC666-701
Marc G Cribbs
Coarctation: A Review
description Coarctation of the aorta occurs in 0.04% of the population, and accounts for approximately 10% of lesions in adults with congenital heart disease. It can occur as an isolated lesion or as a part of a complex defect, and is most commonly associated with bicuspid aortic valve, ventricular septal defect, and mitral valve abnormalities. Since the first surgical repair in 1944, the available treatment options have expanded greatly. Perhaps one of the most important advances in the management of coarctation of the aorta has been the development of transcatheter therapy for both native and especially recurrent coarctation of the aorta. Late complications, even after apparently successful treatment, are not uncommon. For this reason, lifelong follow-up is vital.
format article
author Marc G Cribbs
author_facet Marc G Cribbs
author_sort Marc G Cribbs
title Coarctation: A Review
title_short Coarctation: A Review
title_full Coarctation: A Review
title_fullStr Coarctation: A Review
title_full_unstemmed Coarctation: A Review
title_sort coarctation: a review
publisher Radcliffe Medical Media
publishDate 2020
url https://doaj.org/article/cbee9634a31d4129b8cc3a3861c983b4
work_keys_str_mv AT marcgcribbs coarctationareview
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