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Suspected hyponatremia-induced Brugada phenocopy

Brugada syndrome is a genetic condition that predisposes to an increased risk of ventricular fibrillation and sudden cardiac death in a structurally normal heart. The Brugada type 1 electrocardiogram (ECG) pattern may occur independently of the actual syndrome, and this clinical phenomenon is often...

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Autores principales: Ramsaroop, Koomatie, Seecheran, Rajeev, Seecheran, Valmiki, Persad, Sangeeta, Giddings, Stanley, Mohammed, Boris, Seecheran, Naveen Anand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398420/
https://www.ncbi.nlm.nih.gov/pubmed/30881148
http://dx.doi.org/10.2147/IMCRJ.S200201
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author Ramsaroop, Koomatie
Seecheran, Rajeev
Seecheran, Valmiki
Persad, Sangeeta
Giddings, Stanley
Mohammed, Boris
Seecheran, Naveen Anand
author_facet Ramsaroop, Koomatie
Seecheran, Rajeev
Seecheran, Valmiki
Persad, Sangeeta
Giddings, Stanley
Mohammed, Boris
Seecheran, Naveen Anand
author_sort Ramsaroop, Koomatie
collection PubMed
description Brugada syndrome is a genetic condition that predisposes to an increased risk of ventricular fibrillation and sudden cardiac death in a structurally normal heart. The Brugada type 1 electrocardiogram (ECG) pattern may occur independently of the actual syndrome, and this clinical phenomenon is often referred to as Brugada phenocopy. There are several other factors which have been known to induce this electrocardiographic pattern, and currently, there is a paucity of literature with respect to the pattern that is observed in patients with electrolyte disturbances, specifically hyponatremia. This case report highlights a suspected hyponatremia-induced Brugada type 1 ECG pattern, which subsequently normalized following resolution of the electrolyte derangement.
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spelling pubmed-63984202019-03-16 Suspected hyponatremia-induced Brugada phenocopy Ramsaroop, Koomatie Seecheran, Rajeev Seecheran, Valmiki Persad, Sangeeta Giddings, Stanley Mohammed, Boris Seecheran, Naveen Anand Int Med Case Rep J Case Report Brugada syndrome is a genetic condition that predisposes to an increased risk of ventricular fibrillation and sudden cardiac death in a structurally normal heart. The Brugada type 1 electrocardiogram (ECG) pattern may occur independently of the actual syndrome, and this clinical phenomenon is often referred to as Brugada phenocopy. There are several other factors which have been known to induce this electrocardiographic pattern, and currently, there is a paucity of literature with respect to the pattern that is observed in patients with electrolyte disturbances, specifically hyponatremia. This case report highlights a suspected hyponatremia-induced Brugada type 1 ECG pattern, which subsequently normalized following resolution of the electrolyte derangement. Dove Medical Press 2019-02-27 /pmc/articles/PMC6398420/ /pubmed/30881148 http://dx.doi.org/10.2147/IMCRJ.S200201 Text en © 2019 Ramsaroop et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Case Report
Ramsaroop, Koomatie
Seecheran, Rajeev
Seecheran, Valmiki
Persad, Sangeeta
Giddings, Stanley
Mohammed, Boris
Seecheran, Naveen Anand
Suspected hyponatremia-induced Brugada phenocopy
title Suspected hyponatremia-induced Brugada phenocopy
title_full Suspected hyponatremia-induced Brugada phenocopy
title_fullStr Suspected hyponatremia-induced Brugada phenocopy
title_full_unstemmed Suspected hyponatremia-induced Brugada phenocopy
title_short Suspected hyponatremia-induced Brugada phenocopy
title_sort suspected hyponatremia-induced brugada phenocopy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398420/
https://www.ncbi.nlm.nih.gov/pubmed/30881148
http://dx.doi.org/10.2147/IMCRJ.S200201
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