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Arrhythmogenic Mitral Valve Prolapse

Mitral valve prolapse (MVP) is a common condition present in 1–3% of the population. There has been evidence that a subset of MVP patients is at higher risk of sudden cardiac death. The arrhythmogenic mechanism is related to fibrotic changes in the papillary muscles caused by the prolapsing valve. E...

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Autores principales: Korovesis, Theofanis George, Koutrolou-Sotiropoulou, Paraskevi, Katritsis, Demosthenes George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Radcliffe Cardiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376835/
https://www.ncbi.nlm.nih.gov/pubmed/35990107
http://dx.doi.org/10.15420/aer.2021.28
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author Korovesis, Theofanis George
Koutrolou-Sotiropoulou, Paraskevi
Katritsis, Demosthenes George
author_facet Korovesis, Theofanis George
Koutrolou-Sotiropoulou, Paraskevi
Katritsis, Demosthenes George
author_sort Korovesis, Theofanis George
collection PubMed
description Mitral valve prolapse (MVP) is a common condition present in 1–3% of the population. There has been evidence that a subset of MVP patients is at higher risk of sudden cardiac death. The arrhythmogenic mechanism is related to fibrotic changes in the papillary muscles caused by the prolapsing valve. ECG features include ST-segment depression, T wave inversion or biphasic T waves in inferior leads, and premature ventricular contractions arising from the papillary muscles and the fascicular system. Echocardiography can identify MVP and mitral annular disjunction, a feature that has significant negative prognostic value in MVP. Cardiac MRI is indicated for identifying fibrosis. Patients with high-risk features should be referred for further evaluation. Catheter ablation and mitral valve repair might reduce the risk of malignant arrhythmia. MVP patients with high-risk features and clinically documented ventricular arrhythmia may also be considered for an ICD.
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spelling pubmed-93768352022-08-18 Arrhythmogenic Mitral Valve Prolapse Korovesis, Theofanis George Koutrolou-Sotiropoulou, Paraskevi Katritsis, Demosthenes George Arrhythm Electrophysiol Rev Arrhythmia Risk and Stratification Mitral valve prolapse (MVP) is a common condition present in 1–3% of the population. There has been evidence that a subset of MVP patients is at higher risk of sudden cardiac death. The arrhythmogenic mechanism is related to fibrotic changes in the papillary muscles caused by the prolapsing valve. ECG features include ST-segment depression, T wave inversion or biphasic T waves in inferior leads, and premature ventricular contractions arising from the papillary muscles and the fascicular system. Echocardiography can identify MVP and mitral annular disjunction, a feature that has significant negative prognostic value in MVP. Cardiac MRI is indicated for identifying fibrosis. Patients with high-risk features should be referred for further evaluation. Catheter ablation and mitral valve repair might reduce the risk of malignant arrhythmia. MVP patients with high-risk features and clinically documented ventricular arrhythmia may also be considered for an ICD. Radcliffe Cardiology 2022-04 /pmc/articles/PMC9376835/ /pubmed/35990107 http://dx.doi.org/10.15420/aer.2021.28 Text en Copyright © 2022, Radcliffe Cardiology https://creativecommons.org/licenses/by-nc/4.0/This work is open access under the CC-BY-NC 4.0 License which allows users to copy, redistribute and make derivative works for non-commercial purposes, provided the original work is cited correctly.
spellingShingle Arrhythmia Risk and Stratification
Korovesis, Theofanis George
Koutrolou-Sotiropoulou, Paraskevi
Katritsis, Demosthenes George
Arrhythmogenic Mitral Valve Prolapse
title Arrhythmogenic Mitral Valve Prolapse
title_full Arrhythmogenic Mitral Valve Prolapse
title_fullStr Arrhythmogenic Mitral Valve Prolapse
title_full_unstemmed Arrhythmogenic Mitral Valve Prolapse
title_short Arrhythmogenic Mitral Valve Prolapse
title_sort arrhythmogenic mitral valve prolapse
topic Arrhythmia Risk and Stratification
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376835/
https://www.ncbi.nlm.nih.gov/pubmed/35990107
http://dx.doi.org/10.15420/aer.2021.28
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