TY - JOUR
T1 - Proposed diagnostic criteria for arrhythmogenic cardiomyopathy. European Task Force consensus report
AU - Domenico, Corrado
AU - Aris, Anastasakis
AU - Cristina, Basso
AU - Barbara, Bauce
AU - Carina, Blomström-Lundqvist
AU - Chiara, Bucciarelli-Ducci
AU - Alberto, Cipriani
AU - Carlo, De Asmundis
AU - Estelle, Gandjbakhch
AU - Juan, J Iménez-Jaimez
AU - Maria, Kharlap
AU - McKenna William, J
AU - Lorenzo, Monserrat
AU - James, Moon
AU - Antonis, Pantazis
AU - Antonio, Pelliccia
AU - Martina, Perazzolo Marra
AU - Kalliopi, Pillichou
AU - Jeanette, Schulz-Menger
AU - Ruxandra, Jurcut
AU - Petar, Seferovic
AU - Sanjay, Sharma
AU - Jacob, Tfelt-Hansen
AU - Gaetano, Thiene
AU - Thomas, Wichter
AU - Arthur, Wilde
AU - Alessandro, Zorzi
N1 - Copyright © 2023. Published by Elsevier B.V.
PY - 2024/1/15
Y1 - 2024/1/15
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85175465239&partnerID=8YFLogxK
U2 - 10.1016/j.ijcard.2023.131447
DO - 10.1016/j.ijcard.2023.131447
M3 - Journal article
C2 - 37844667
SN - 0167-5273
VL - 395
SP - 1
EP - 13
JO - International Journal of Cardiology
JF - International Journal of Cardiology
M1 - 131447
ER -