Suppr超能文献

肥厚型心肌病

Hypertrophic cardiomyopathy.

作者信息

Antunes Murillo de Oliveira, Scudeler Thiago Luis

机构信息

Instituto do Coração (InCor), Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Universidade São Francisco (USF), Bragança Paulista, São Paulo, Brazil.

出版信息

Int J Cardiol Heart Vasc. 2020 Mar 25;27:100503. doi: 10.1016/j.ijcha.2020.100503. eCollection 2020 Apr.

Abstract

Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disease. The disease is characterized by marked variability in morphological expression and natural history, ranging from asymptomatic to heart failure or sudden cardiac death. Left ventricular hypertrophy and abnormal ventricular configuration result in dynamic left ventricular outflow obstruction in most patients. The goal of pharmacological therapy in HCM is to alleviate the symptoms, and it includes pharmacotherapies and septal reduction therapies. In this review, we summarize the relevant clinical issues and treatment options of HCM.

摘要

肥厚型心肌病(HCM)是最常见的遗传性心脏病。该疾病的特征是形态学表现和自然病史存在显著差异,范围从无症状到心力衰竭或心源性猝死。左心室肥厚和异常的心室形态在大多数患者中导致动态左心室流出道梗阻。HCM的药物治疗目标是缓解症状,包括药物治疗和减隔治疗。在本综述中,我们总结了HCM的相关临床问题和治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5286/7154317/b2e95fa48f75/gr1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验