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

被引:48
|
作者
Corrado, Domenico [1 ]
Anastasakis, Aris [2 ]
Basso, Cristina [1 ]
Bauce, Barbara [1 ]
Blomstrom-Lundqvist, Carina [3 ]
Bucciarelli-Ducci, Chiara [4 ]
Cipriani, Alberto [1 ]
De Asmundis, Carlo [5 ]
Gandjbakhch, Estelle [6 ]
Jimenez-Jaimez, Juan [7 ]
Kharlap, Maria [8 ]
McKenna, William J. [9 ]
Monserrat, Lorenzo [10 ]
Moon, James [11 ]
Pantazis, Antonis [12 ]
Pelliccia, Antonio [13 ]
Marra, Martina Perazzolo [1 ]
Pillichou, Kalliopi [1 ]
Schulz-Menger, Jeanette [14 ]
Jurcut, Ruxandra [15 ]
Seferovic, Petar [16 ,17 ]
Sharma, Sanjay [18 ]
Tfelt-Hansen, Jacob [19 ,20 ]
Thiene, Gaetano [21 ]
Wichter, Thomas [22 ]
Wilde, Arthur [23 ]
Zorzi, Alessandro [1 ]
机构
[1] Univ Padua, Dept Cardiothoracovasc Sci & Publ Hlth, Med Sch, Padua, Italy
[2] Onassis Cardiac Surg Ctr, Unit Inherited & Rare Cardiovasc Dis, Athens, Greece
[3] Orebro Univ, Fac Med & Hlth, Sch Med Sci, Dept Cardiol, Orebro, Sweden
[4] Bromptom Royal Hosp, CMR Serv, London, England
[5] Brussel Vrije Univ Brussel, Univ Ziekenhuis, Heart Rhythm Management Ctr, Postgrad Program Cardiac Electrophysiol & Pacing, Brussels, Belgium
[6] Sorbonne Univ, Grp Hosp Pitie Salpetriere Charles Foix, AP HP, Ctr Reference Malad Cardiaques Hereditaires, Paris, France
[7] Univ Hosp, Cardiac Electrophysiol Ctr, Burgos, Spain
[8] Natl Ctr Therapy & Prevent Med, Dept Cardiac Arrhythmias, Moscow, Petroverigsky, Russia
[9] UCL, Inst Cardiovasc Sci, London, England
[10] Dilemma Solut SL, Dept Med, Cardiovasc Genet, La Coruna, Spain
[11] UCL, Barts Heart Ctr, CMR Serv, London, England
[12] Royal Brompton & Harefield Hosp, Inherited Cardiovasc Condit Serv, London, England
[13] Inst Sport Med & Sci, Rome, Italy
[14] Charite Univ Med Berlin, Campus Buch ECRC & Helios Clin, DZHK Partnersite Berlin, Berlin, Germany
[15] UMF Carol Davila, Expert Ctr Rare Genet Cardiovasc Dis, Inst Cardiovasc Dis Prof Dr CC Iliescu, Bucharest, Romania
[16] Univ Belgrade, Fac Med, Belgrade, Serbia
[17] Univ Belgrade, Heart Failure Ctr, Med Ctr, Belgrade, Serbia
[18] St Georges Univ London, Cardiol Clin Acad Grp, London, England
[19] Univ Copenhagen, Fac Med Sci, Dept Forens Med, Sect Genet, Copenhagen, Denmark
[20] Copenhagen Univ Hosp, Heart Ctr, Dept Cardiol, Rigshospitalet, Copenhagen, Denmark
[21] Padova Univ, ARCA Assoc Ricerche Cardiopatie Aritm ETS, Sch Med, Padua, Italy
[22] Marien Hosp, Dept Internal Med & Cardiol, Heart Ctr Osnabruck Bad Rothenfelde, Niels Stensen Kliniken, Osnabruck, Germany
[23] Univ Amsterdam, Dept Cardiol, Amsterdam UMC Locat, Amsterdam, Netherlands
关键词
Cardiac magnetic resonance; Cardiomyopathy; Diagnosis; Ventricular arrhythmia; Sudden death; RIGHT-VENTRICULAR CARDIOMYOPATHY; CARDIAC MAGNETIC-RESONANCE; T-WAVE INVERSION; GADOLINIUM ENHANCEMENT; MYOCARDIAL FIBROSIS; MUTATION CARRIERS; SUDDEN-DEATH; RISK; TACHYCARDIA; SCAR;
D O I
10.1016/j.ijcard.2023.131447
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 abnor-malities 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.
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页数:13
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