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Diagnosis and management of hypertrophic cardiomyopathy

The clinical spectrum of hypertrophic cardiomyopathy (HCM) is complex and includes a variety of phenotypes, which leads to different types of manifestations. Although most of the patients are asymptomatic, a significant proportion of them will develop symptoms or risk of arrhythmias and sudden cardi...

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Autores principales: Pantazis, Antonis, Vischer, Annina S, Perez-Tome, Maria Carrillo, Castelletti, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676455/
https://www.ncbi.nlm.nih.gov/pubmed/26693331
http://dx.doi.org/10.1530/ERP-15-0007
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author Pantazis, Antonis
Vischer, Annina S
Perez-Tome, Maria Carrillo
Castelletti, Silvia
author_facet Pantazis, Antonis
Vischer, Annina S
Perez-Tome, Maria Carrillo
Castelletti, Silvia
author_sort Pantazis, Antonis
collection PubMed
description The clinical spectrum of hypertrophic cardiomyopathy (HCM) is complex and includes a variety of phenotypes, which leads to different types of manifestations. Although most of the patients are asymptomatic, a significant proportion of them will develop symptoms or risk of arrhythmias and sudden cardiac death (SCD). Therefore, the objectives of HCM diagnosis and management are to relieve the patients' symptoms (chest pain, heart failure, syncope, palpitations, etc.), prevent disease progression and major cardiovascular complications and SCD. The heterogeneity of HCM patterns, their symptoms and assessment is a challenge for the cardiologist.
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spelling pubmed-46764552015-12-21 Diagnosis and management of hypertrophic cardiomyopathy Pantazis, Antonis Vischer, Annina S Perez-Tome, Maria Carrillo Castelletti, Silvia Echo Res Pract Review The clinical spectrum of hypertrophic cardiomyopathy (HCM) is complex and includes a variety of phenotypes, which leads to different types of manifestations. Although most of the patients are asymptomatic, a significant proportion of them will develop symptoms or risk of arrhythmias and sudden cardiac death (SCD). Therefore, the objectives of HCM diagnosis and management are to relieve the patients' symptoms (chest pain, heart failure, syncope, palpitations, etc.), prevent disease progression and major cardiovascular complications and SCD. The heterogeneity of HCM patterns, their symptoms and assessment is a challenge for the cardiologist. Bioscientifica Ltd 2015-03-11 2015-03-01 /pmc/articles/PMC4676455/ /pubmed/26693331 http://dx.doi.org/10.1530/ERP-15-0007 Text en © 2015 The authors http://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Review
Pantazis, Antonis
Vischer, Annina S
Perez-Tome, Maria Carrillo
Castelletti, Silvia
Diagnosis and management of hypertrophic cardiomyopathy
title Diagnosis and management of hypertrophic cardiomyopathy
title_full Diagnosis and management of hypertrophic cardiomyopathy
title_fullStr Diagnosis and management of hypertrophic cardiomyopathy
title_full_unstemmed Diagnosis and management of hypertrophic cardiomyopathy
title_short Diagnosis and management of hypertrophic cardiomyopathy
title_sort diagnosis and management of hypertrophic cardiomyopathy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676455/
https://www.ncbi.nlm.nih.gov/pubmed/26693331
http://dx.doi.org/10.1530/ERP-15-0007
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