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Bicuspid Aortic Valvulopathy and Associated Aortopathy: a Review of Contemporary Studies Relevant to Clinical Decision-Making

机译:Bicuspid主动脉瓣病变和相关性感病变:对与临床决策相关的当代研究综述

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The bicuspid aortic valve (BAV) phenotype is becoming increasingly recognized as a complex and heterogeneous clinical entity, with some but not all patients developing accelerated degrees of both aortic insufficiency (AI) and aortic stenosis (AS) in comparison to patients with tricuspid aortic valves (TAV). In addition, there remains a well-established association between the BAV phenotype and aortic enlargement independent of valve function as well as progression among some to ascending aortic aneurysm and the attendant concern over risk of aortic dissection. Because the understanding of the complexity of the BAV phenotype is evolving as quickly as are the options for medical, surgical, and interventional therapy, this review aims to provide an update on the most clinically relevant recent advances in the realm of BAV and associated aortopathy from a genetic, morphologic, and clinical outcomes perspective in order to give the practicing clinician a deeper understanding of how to approach both medical and surgical decision-making in the patient with BAV. The following major principles have emerged in recent years including (1) the importance of cusp anatomy and its implications on the long-term risk of AI, aortic dilation, and aortic dissection, (2) the role of post-valvular flow dynamics in the pathogenesis of aortic dilation in BAV patients, (3) the ability of aortic valve replacement to halt accelerated dilation rates, and (4) the finding that the risk of aortic dissection, while still overall intermediate is much more akin to the baseline risk present in TAV patients rather than the much higher rates observed in patients with Marfan's disease. Together, these data support the less aggressive approach to aortic replacement in BAV patients as reflected in the most recent ACC/AHA guidelines and provide a stronger basis upon which future studies, including those aimed at medical and transcatheter therapies, stand to make further impact on our ability to optimally treat this epidemiologically important and complex population of patients.
机译:双囊主动脉瓣(BAV)表型越来越越来越被认为是复杂和异质的临床实体,其中一些但并非所有患者都与Tricuspid主动脉瓣的患者相比,开发主动脉内容不全(AI)和主动脉狭窄(AS)的加速程度(TAV)。此外,BAV表型和主动脉扩大之间仍然存在良好的关联,与阀功能无关以及一些升高主动脉动脉瘤的进展以及伴随着对主动脉裂解的危险的关注。由于了解BAV表型的复杂性,尽可能快地发展,因此,本综述旨在提供关于BAV和相关主动病域领域最近最近进步的更新遗传,形态学和临床结果的视角,使练习临床医生更深入地了解如何在患者中接近医疗和手术决策。近年来出现了以下主要原则,其中包括(1)尖头解剖学的重要性及其对AI,主动脉扩张和主动脉夹层的长期风险的影响,(2)后瓣膜流动动力学的作用BAV患者主动脉扩张的发病机制(3)主动脉瓣置换止扰加速扩张率的能力,以及(4)诱导主动脉解剖的风险,同时仍然总体中间体更加类似于存在的基线风险TAV患者而不是Marfan疾病患者观察到的更高率。这些数据在一起,支持BAV患者的主动脉替代性较少的侵略性方法,如最近的ACC / AHA指南所反映,并在哪些研究的基础上提供更强大的基础,包括针对医疗和经转截管疗法的人,立即产生进一步影响我们能够最佳地治疗这种流行病学且复杂的患者人口。

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