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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Bioscientifica Ltd
2015
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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. |
format | Online Article Text |
id | pubmed-4676455 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Bioscientifica Ltd |
record_format | MEDLINE/PubMed |
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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