ABC | Volume 112, Nº1, Janeiro 2019

Elias Neto et al C/DAVD – Diagnóstico e tratamento Arq Bras Cardiol. 2019; 112(1):91-103 Artigo de Revisão Este é um artigo de acesso aberto distribuído sob os termos da licença de atribuição pelo Creative Commons 28. Bai R, Di Biase L, Shivkumar K, Mohanty P, Tung R, Santangeli P, et al. Ablation of ventricular arrhythmias in arrhythmogenic right ventricular dysplasia/ cardiomyopathy:arrhythmia-freesurvivalafterendo-epicardialsubstratebased mapping and ablation. Circ ArrhythmElectrophysiol. 2011;4(4):478-85. 29. Birnie DH, Nery PB, Ha AC, Beanlands RSB. Cardiac sarcoidosis. J Am Coll Cardiol. 2016; 68(4):411-21. 30. Corrado D, Zorzi A, Cerrone M, Rigato I, Mongillo M, Bauce B, et al. Relationship between arrhythmogenic right ventricular cardiomyopathy and Brugada Syndrome: new insights from molecular biology and clinical implications. Circ Arrhythm Electrophysiol. 2016;9(4):e003631. 31. Scheinman MM. Is the Brugada Syndrome a distinct clinical entity? J Cardiovasc Electrophysiol. 1997;8(3):332-6. 32. Zumhagen S, Spieker T, Rolinck J, Baba HA, Breithardt G, Böcker W, et al. Absence of pathognomonic or inflammatory patterns in cardiac biopsies from patients with Brugada Syndrome. Circ Arrhythm Electrophysiol. 2009;2(1):16-23. 33. Frustaci A, Priori SG, Pieroni M, Chimenti C, Napolitano C, Rivolta I, et al. Cardiac histological substrate in patients with clinical phenotype of Brugada Syndrome. Circulation. 2005; 112(24):3680-7. 34. Corrado D,Wichter T, Link MS, Hauer RN, Marchlinski FE, Anastasakis A, et al. Treatment of arrhythmogenic right ventricular cardiomyopathy/ dysplasia - an International Task Force Consensus Statement. Circulation. 2015;132(5):441-53. 35. Maron BJ, Udelson JE, Bonow RO, Nishimura RA, Ackerman MJ, Estes NA 3rd, et al. Eligibility and disqualification recommendations for competitive athletes with cardiovascular abnormalities: Task Force 3: hypertrophic cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy and other cardiomyopathies, and myocarditis: a scientific statement from the American Heart Association and American College of Cardiology. Circulation. 2015;132(22): e 273-80. 36. Tonet J, Frank R, Fontaine G, Grosgogeat Y. Efficacy and safety of low doses of beta-blocker agents combined with amiodarone in refractory ventricular tachycardia. Pacing Clin Electrophysiol. 1988;11(11 Pt 2):1984-9. 37. Ermakov S, Gerstenfeld EP, Svetlichnaya Y, ScheinmanMM.Use of flecainide in combination antiarrhythmic therapy in patients with arrhythmogenic right ventricular cardiomyopathy. Heart Rhythm. 2017;14(4):564-9. 38. Philips B, Madhavan S, James C, Tichnell C, Murray B, Dalal D, et al. Outcomes of catheter ablation of ventricular tachycardia in arrhythmogenic right ventricular dysplasia/cardiomyopathy. Circ Arrhythm Electrophysiol. 2012;5(3):499-505. 39. VermaA,KilicaslanF,SchweikertRA,TomassoniG,RossilloA,MarroucheNF, et al. Short- and long-term success of substrate-basedmapping and ablation of ventricular tachycardia in arrhythmogenic right ventricular dysplasia. Circulation. 2005;111(24):3209-16. 40. Dalal D, Jain R, Tandri H, Dong J, Eid SM, Prakasa K, et al. Long-term efficacy of catheter ablation of ventricular tachycardia in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy. J Am Coll Cardiol. 2007;50(5):432-40. 41. Miljoen H, State S, Chillou C, Magnin-Poull I, Dotto P, Andronache M, et al. Electroanatomic mapping characteristics of ventricular tachycardia in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia. Europace. 2005;7(6):516-24. 42. Link MS, Laidlaw D, Polonsky B, Zareba W, McNitt S, Gear K, et al. Ventricular arrhythmias in the North American multidisciplinary study of ARVC: predictors, characteristics, and treatment. J Am Coll Cardiol. 2014;64(2):119-25. 13

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