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To Be or Not to Be Eisenmenger: The Different Shades of Blue

Eisenmenger syndrome refers to any untreated congenital cardiac defect with an intracardiac communication that leads to pulmonary arterial hypertension, reversal of intracardiac shunting, and cyanosis. We describe a 40-year-old cyanotic patient with congenital heart disease with presumed Eisenmenger...

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Autores principales: Cohen, Sarit S., Nageshwaran, Sathiji Kathiresu, Murthy, Raghav, Chan, Alice, Cohen, Jennifer, Jhaveri, Simone, Love, Barry, Zaidi, Ali N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310966/
https://www.ncbi.nlm.nih.gov/pubmed/34317508
http://dx.doi.org/10.1016/j.jaccas.2020.12.026
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author Cohen, Sarit S.
Nageshwaran, Sathiji Kathiresu
Murthy, Raghav
Chan, Alice
Cohen, Jennifer
Jhaveri, Simone
Love, Barry
Zaidi, Ali N.
author_facet Cohen, Sarit S.
Nageshwaran, Sathiji Kathiresu
Murthy, Raghav
Chan, Alice
Cohen, Jennifer
Jhaveri, Simone
Love, Barry
Zaidi, Ali N.
author_sort Cohen, Sarit S.
collection PubMed
description Eisenmenger syndrome refers to any untreated congenital cardiac defect with an intracardiac communication that leads to pulmonary arterial hypertension, reversal of intracardiac shunting, and cyanosis. We describe a 40-year-old cyanotic patient with congenital heart disease with presumed Eisenmenger syndrome who was considered inoperable. Testing revealed a partial atrioventricular septal defect with no evidence of pulmonary arterial hypertension, and the patient underwent successful cardiac repair. (Level of Difficulty: Intermediate.)
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spelling pubmed-83109662021-07-26 To Be or Not to Be Eisenmenger: The Different Shades of Blue Cohen, Sarit S. Nageshwaran, Sathiji Kathiresu Murthy, Raghav Chan, Alice Cohen, Jennifer Jhaveri, Simone Love, Barry Zaidi, Ali N. JACC Case Rep Mini-Focus Issue: Congenital Heart Disease Eisenmenger syndrome refers to any untreated congenital cardiac defect with an intracardiac communication that leads to pulmonary arterial hypertension, reversal of intracardiac shunting, and cyanosis. We describe a 40-year-old cyanotic patient with congenital heart disease with presumed Eisenmenger syndrome who was considered inoperable. Testing revealed a partial atrioventricular septal defect with no evidence of pulmonary arterial hypertension, and the patient underwent successful cardiac repair. (Level of Difficulty: Intermediate.) Elsevier 2021-02-17 /pmc/articles/PMC8310966/ /pubmed/34317508 http://dx.doi.org/10.1016/j.jaccas.2020.12.026 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Mini-Focus Issue: Congenital Heart Disease
Cohen, Sarit S.
Nageshwaran, Sathiji Kathiresu
Murthy, Raghav
Chan, Alice
Cohen, Jennifer
Jhaveri, Simone
Love, Barry
Zaidi, Ali N.
To Be or Not to Be Eisenmenger: The Different Shades of Blue
title To Be or Not to Be Eisenmenger: The Different Shades of Blue
title_full To Be or Not to Be Eisenmenger: The Different Shades of Blue
title_fullStr To Be or Not to Be Eisenmenger: The Different Shades of Blue
title_full_unstemmed To Be or Not to Be Eisenmenger: The Different Shades of Blue
title_short To Be or Not to Be Eisenmenger: The Different Shades of Blue
title_sort to be or not to be eisenmenger: the different shades of blue
topic Mini-Focus Issue: Congenital Heart Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310966/
https://www.ncbi.nlm.nih.gov/pubmed/34317508
http://dx.doi.org/10.1016/j.jaccas.2020.12.026
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