Aortic stenosis from the perspective of the current guidelines

M. Jelavic, H. Pintarić
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引用次数: 0

Abstract

Aortic stenosis (AS) is one of the most common valvular diseases encountered in clinical practice. It is most frequently caused by degenerative aortic valve fibrosis and calcification, and in a lesser number of cases by the calcification of congenital deformed aortic valve (bicuspid); it may occasionally develop after rheumatic fever. Valve fibrosis and calcification lead to progressive valve restriction, obstruction and increased afterload with left ventricle remodelling for normalization of wall tension and cardiac output. During time, such hypertrophic and fibrotic myocardium deteriorates, resulting in heart failure. Generally, current guidelines of the European Society of Cardiology (ESC) recommend aortic valve replacement (AVR) when the aortic valve is severely stenotic and the patient is symptomatic. Most asymptomatic patients with severe AS should be managed conservatively, except for those with systolic LV dysfunction, an abnormal exercise test, very severe aortic stenosis, severe valve calcification, markedly elevated cardiac biomarkers, and severe pulmonary hypertension without other explanation. This article will review our current understanding of the pathophysiology of AS and provide detailed information about clinical presentation, diagnostic procedures, disease course, and different treatment strategies for various groups of these patients.
从目前的主动脉瓣狭窄指南来看
主动脉瓣狭窄是临床上最常见的瓣膜疾病之一。它最常由退行性主动脉瓣纤维化和钙化引起,少数病例由先天性畸形主动脉瓣(二尖瓣)钙化引起;偶尔在风湿热后出现。瓣膜纤维化和钙化导致进行性瓣膜受限、梗阻和后负荷增加,左心室重构使壁张力和心输出量正常化。随着时间的推移,这种肥厚和纤维化的心肌恶化,导致心力衰竭。一般来说,欧洲心脏病学会(ESC)目前的指南建议在主动脉瓣严重狭窄且患者有症状时进行主动脉瓣置换术(AVR)。大多数无症状的严重AS患者应保守治疗,除了那些有收缩期左室功能障碍、运动试验异常、非常严重的主动脉狭窄、严重的瓣膜钙化、心脏生物标志物明显升高和无其他解释的严重肺动脉高压的患者。本文将回顾我们目前对AS病理生理学的理解,并提供有关临床表现、诊断程序、病程以及不同类型患者的不同治疗策略的详细信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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