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致心律失常性心肌病的拟议诊断标准:欧洲工作组共识报告。

Proposed diagnostic criteria for arrhythmogenic cardiomyopathy: European Task Force consensus report.

作者信息

Corrado Domenico, Anastasakis Aris, Basso Cristina, Bauce Barbara, Blomström-Lundqvist Carina, Bucciarelli-Ducci Chiara, Cipriani Alberto, De Asmundis Carlo, Gandjbakhch Estelle, Jiménez-Jáimez Juan, Kharlap Maria, McKenna William J, Monserrat Lorenzo, Moon James, Pantazis Antonis, Pelliccia Antonio, Perazzolo Marra Martina, Pillichou Kalliopi, Schulz-Menger Jeanette, Jurcut Ruxandra, Seferovic Petar, Sharma Sanjay, Tfelt-Hansen Jacob, Thiene Gaetano, Wichter Thomas, Wilde Arthur, Zorzi Alessandro

机构信息

Department of Cardio-Thoraco-Vascular Sciences and Public Health, University of Padua Medical School, Italy.

Unit of Inherited and Rare Cardiovascular Diseases, Onassis Cardiac Surgery Center, Athens, Greece.

出版信息

Int J Cardiol. 2024 Jan 15;395:131447. doi: 10.1016/j.ijcard.2023.131447. Epub 2023 Oct 14.

Abstract

Arrhythmogenic cardiomyopathy (ACM) is a heart muscle disease characterized by prominent "non-ischemic" myocardial scarring predisposing to ventricular electrical instability. Diagnostic criteria for the original phenotype, arrhythmogenic right ventricular cardiomyopathy (ARVC), were first proposed in 1994 and revised in 2010 by an international Task Force (TF). A 2019 International Expert report appraised these previous criteria, finding good accuracy for diagnosis of ARVC but a lack of sensitivity for identification of the expanding phenotypic disease spectrum, which includes left-sided variants, i.e., biventricular (ABVC) and arrhythmogenic left ventricular cardiomyopathy (ALVC). The ARVC phenotype together with these left-sided variants are now more appropriately named ACM. The lack of diagnostic criteria for the left ventricular (LV) phenotype has resulted in clinical under-recognition of ACM patients over the 4 decades since the disease discovery. In 2020, the "Padua criteria" were proposed for both right- and left-sided ACM phenotypes. The presently proposed criteria represent a refinement of the 2020 Padua criteria and have been developed by an expert European TF to improve the diagnosis of ACM with upgraded and internationally recognized criteria. The growing recognition of the diagnostic role of CMR has led to the incorporation of myocardial tissue characterization findings for detection of myocardial scar using the late‑gadolinium enhancement (LGE) technique to more fully characterize right, biventricular and left disease variants, whether genetic or acquired (phenocopies), and to exclude other "non-scarring" myocardial disease. The "ring-like' pattern of myocardial LGE/scar is now a recognized diagnostic hallmark of ALVC. Additional diagnostic criteria regarding LV depolarization and repolarization ECG abnormalities and ventricular arrhythmias of LV origin are also provided. These proposed upgrading of diagnostic criteria represents a working framework to improve management of ACM patients.

摘要

致心律失常性心肌病(ACM)是一种心肌疾病,其特征为显著的“非缺血性”心肌瘢痕形成,易导致心室电不稳定。1994年首次提出了原始表型致心律失常性右室心肌病(ARVC)的诊断标准,并于2010年由一个国际特别工作组(TF)进行了修订。2019年的一份国际专家报告对这些先前的标准进行了评估,发现其对ARVC的诊断具有良好的准确性,但对于识别不断扩大的表型疾病谱缺乏敏感性,该疾病谱包括左侧变异型,即双心室(ABVC)和致心律失常性左室心肌病(ALVC)。ARVC表型以及这些左侧变异型现在更恰当地称为ACM。自该疾病发现以来的40年里,由于缺乏左室(LV)表型的诊断标准,导致ACM患者在临床上未得到充分认识。2020年,针对右侧和左侧ACM表型提出了“帕多瓦标准”。目前提出的标准是对2020年帕多瓦标准的细化,由一个欧洲专家特别工作组制定,以通过升级的国际认可标准改进ACM的诊断。对CMR诊断作用的日益认识导致纳入了心肌组织特征分析结果,以使用延迟钆增强(LGE)技术检测心肌瘢痕,从而更全面地表征右侧、双心室和左侧疾病变异型,无论其是遗传性还是获得性(表型模拟),并排除其他“无瘢痕”心肌疾病。心肌LGE/瘢痕的“环状”模式现在是ALVC公认的诊断标志。还提供了关于LV去极化和复极化心电图异常以及LV起源的室性心律失常的其他诊断标准。这些提议的诊断标准升级代表了一个改善ACM患者管理的工作框架。

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