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A hol(e)y predicament
Endocardial cushion defects are congenital abnormalities that result in valvular dysfunction as well as defects (or “holes”) in the septa of the heart. They are typically diagnosed in early infancy; presentation late in life is rare. We present the case of a 72‐year‐old female admitted to the hospit...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398964/ https://www.ncbi.nlm.nih.gov/pubmed/28435681 http://dx.doi.org/10.1002/rcr2.237 |
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author | Meka, Shaiva Ginoya Shelden, Daniel Mertens, Amy Christensen, Paul Patel, Meet |
author_facet | Meka, Shaiva Ginoya Shelden, Daniel Mertens, Amy Christensen, Paul Patel, Meet |
author_sort | Meka, Shaiva Ginoya |
collection | PubMed |
description | Endocardial cushion defects are congenital abnormalities that result in valvular dysfunction as well as defects (or “holes”) in the septa of the heart. They are typically diagnosed in early infancy; presentation late in life is rare. We present the case of a 72‐year‐old female admitted to the hospital with dyspnoea and palpitations. She was found to have multifocal atrial tachycardia. She suffered cardiac arrest associated with refractory hypoxaemia that required mechanical ventilation and vasodilator therapy with inhaled nitric oxide. Echocardiography revealed a large ostium primum atrial septal defect (ASD) complicated by Eisenmenger syndrome. It is likely that her arrhythmia, a sequela from her long‐standing congenital abnormality, led to sudden decompensation. In this case presentation, we review the aetiology, presentation, and complications of ASDs. |
format | Online Article Text |
id | pubmed-5398964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53989642017-04-21 A hol(e)y predicament Meka, Shaiva Ginoya Shelden, Daniel Mertens, Amy Christensen, Paul Patel, Meet Respirol Case Rep Case Reports Endocardial cushion defects are congenital abnormalities that result in valvular dysfunction as well as defects (or “holes”) in the septa of the heart. They are typically diagnosed in early infancy; presentation late in life is rare. We present the case of a 72‐year‐old female admitted to the hospital with dyspnoea and palpitations. She was found to have multifocal atrial tachycardia. She suffered cardiac arrest associated with refractory hypoxaemia that required mechanical ventilation and vasodilator therapy with inhaled nitric oxide. Echocardiography revealed a large ostium primum atrial septal defect (ASD) complicated by Eisenmenger syndrome. It is likely that her arrhythmia, a sequela from her long‐standing congenital abnormality, led to sudden decompensation. In this case presentation, we review the aetiology, presentation, and complications of ASDs. John Wiley & Sons, Ltd 2017-04-20 /pmc/articles/PMC5398964/ /pubmed/28435681 http://dx.doi.org/10.1002/rcr2.237 Text en © 2017 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology 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 Meka, Shaiva Ginoya Shelden, Daniel Mertens, Amy Christensen, Paul Patel, Meet A hol(e)y predicament |
title | A hol(e)y predicament |
title_full | A hol(e)y predicament |
title_fullStr | A hol(e)y predicament |
title_full_unstemmed | A hol(e)y predicament |
title_short | A hol(e)y predicament |
title_sort | hol(e)y predicament |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398964/ https://www.ncbi.nlm.nih.gov/pubmed/28435681 http://dx.doi.org/10.1002/rcr2.237 |
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