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继发性三尖瓣反流:一种被低估但临床相关性日益增加的瓣膜疾病

[Secondary atrial tricuspid regurgitation: an underestimated but increasingly clinically relevant valve disorder].

作者信息

Badano Luigi P, Tomaselli Michele, Fraccaro Chiara, Sannino Anna, Fortuni Federico, Adamo Marianna, Ancona Francesco, Sticchi Alessandro, Camalleri Valeria, Pasquini Annalisa, Cannata Francesco, Masiero Giulia, Golino Paolo, Perrone Filardi Pasquale, Indolfi Ciro, Vizza Carmine Dario, Muraru Denisa

机构信息

Centro di Diagnostica Cardiovascolare Integrata, Istituto Auxologico Italiano, IRCCS, Milano - Dipartimento di Medicina e Chirurgia, Università degli Studi Milano-Bicocca, Milano.

Centro di Diagnostica Cardiovascolare Integrata, Istituto Auxologico Italiano, IRCCS, Milano.

出版信息

G Ital Cardiol (Rome). 2025 Sep;26(9):656-665. doi: 10.1714/4542.45430.

Abstract

Atrial secondary tricuspid regurgitation (A-STR) is a complex and increasingly recognized form of valvular heart disease that arises primarily due to right atrial and tricuspid annular dilation in the absence of intrinsic leaflet pathology. Unlike ventricular secondary tricuspid regurgitation, which is driven by right ventricular remodeling, A-STR is predominantly associated with atrial fibrillation, heart failure with preserved ejection fraction, and other conditions that lead to chronic right atrial remodeling. This condition has been underappreciated despite its significant prevalence and impact on patient morbidity and mortality. Echocardiography is the primary diagnostic tool for diagnosing and assessing patients with A-STR. The natural history of A-STR is unfavorable, with potential worsening over time, particularly if the underlying conditions are not properly treated. Treatment options include cardioversion of atrial fibrillation and medical treatment of heart failure with preserved ejection fraction, which may promote reverse remodeling of the right heart structures and reduce STR severity in some cases. Surgical tricuspid valve annuloplasty remains the gold standard for severe cases, but transcatheter interventions are emerging as potential alternatives. This review provides a comprehensive overview of A-STR, encompassing its epidemiology, pathophysiology, diagnostic approaches, and treatment strategies. By synthesizing current evidence and highlighting gaps in knowledge, this paper aims to guide clinicians in the management of this challenging condition and to inspire future research.

摘要

心房性继发性三尖瓣反流(A-STR)是一种复杂且日益被认识到的心脏瓣膜病形式,主要由于右心房和三尖瓣环扩张而出现,且不存在瓣膜小叶的内在病变。与由右心室重构驱动的心室性继发性三尖瓣反流不同,A-STR主要与心房颤动、射血分数保留的心力衰竭以及其他导致慢性右心房重构的病症相关。尽管这种病症具有较高的患病率且对患者的发病率和死亡率有显著影响,但一直未得到充分认识。超声心动图是诊断和评估A-STR患者的主要诊断工具。A-STR的自然病程不利,随着时间推移可能会恶化,尤其是在潜在病症未得到妥善治疗的情况下。治疗选择包括心房颤动的复律以及射血分数保留的心力衰竭的药物治疗,在某些情况下,这可能促进右心结构的逆向重构并降低STR的严重程度。对于严重病例,外科三尖瓣环成形术仍然是金标准,但经导管介入治疗正逐渐成为潜在的替代方法。本综述全面概述了A-STR,包括其流行病学、病理生理学、诊断方法和治疗策略。通过综合当前证据并突出知识空白,本文旨在指导临床医生管理这一具有挑战性的病症,并激发未来的研究。

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