Literature DB >> 20145349

Clinical course of arrhythmogenic right ventricular cardiomyopathy in the era of implantable cardioverter-defibrillators and radiofrequency catheter ablation.

Masatoshi Komura1, Jun-Ichi Suzuki, Susumu Adachi, Atsushi Takahashi, Kenichiro Otomo, Junichi Nitta, Mitsuhiro Nishizaki, Tohru Obayashi, Akihiko Nogami, Yasuhiro Satoh, Kaoru Okishige, Hitoshi Hachiya, Kenzo Hirao, Mitsuaki Isobe.   

Abstract

This study investigated the clinical course of arrhythmogenic right ventricular cardiomyopathy (ARVC) patients and in particular evaluated the contribution of radiofrequency catheter ablation (RFCA) and an implantable cardioverter-defibrillator (ICD) to the treatment of ARVC. ARVC is a myocardial disorder and a cause of sudden cardiac death due to ventricular tachycardia (VT). Little is known about its prognosis in Japanese ARVC patients. Thirty-five ARVC patients were studied. Mean age of patients whose onset of ARVC was congestive heart failure (CHF) (66.0 +/- 4.0 years) was significantly higher than those whose onset was VT (44.5 +/- 14.8 years, P < 0.05). ARVC patients with CHF onset showed significantly higher death rates compared to those with VT onset. ICD treatment significantly reduced episodes of hospitalization due to VT (0.1 +/- 0.4 episodes) in comparison to treatment by RFCA (1.7 +/- 2.2 episodes, P < 0.03). RFCA treatment did not reduce recurrence of VT in the follow-up period. ICD therapy showed comparable mortality to RFCA treatment. The prognosis of ARVC with CHF onset is poor. ICD therapy significantly reduced hospitalization due to VT compared with RFCA treatment. ICD implantation in combination with medication may be a better treatment for ARVC.

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Year:  2010        PMID: 20145349     DOI: 10.1536/ihj.51.34

Source DB:  PubMed          Journal:  Int Heart J        ISSN: 1349-2365            Impact factor:   1.862


  6 in total

1.  Predictors of appropriate ICD therapy in patients with arrhythmogenic right ventricular cardiomyopathy: long term experience of a tertiary care center.

Authors:  Pia K Schuler; Laurent M Haegeli; Ardan M Saguner; Thomas Wolber; Felix C Tanner; Rolf Jenni; Natascia Corti; Thomas F Lüscher; Corinna Brunckhorst; Firat Duru
Journal:  PLoS One       Date:  2012-09-27       Impact factor: 3.240

2.  Management of a rare case of arrhythmogenic right ventricular dysplasia in pregnancy: a case report.

Authors:  Nilgün Güdücü; Salih Serdar Kutay; Ebru Ozenç; Cavlan Ciftçi; Alin Başgül Yiğiter; Herman Işçi
Journal:  J Med Case Rep       Date:  2011-07-10

Review 3.  Science and practice of arrhythmogenic cardiomyopathy: A paradigm shift.

Authors:  Mohamed Elmaghawry; Federico Migliore; Nazar Mohammed; Despina Sanoudou; Mohammed Alhashemi
Journal:  Glob Cardiol Sci Pract       Date:  2013-11-01

Review 4.  A global perspective of arrhythmogenic right ventricular cardiomyopathy.

Authors:  Mohamed Elmaghawry; Mohammed Alhashemi; Alessandro Zorzi; Magdi H Yacoub
Journal:  Glob Cardiol Sci Pract       Date:  2013-11-01

5.  Failure of ICD therapy in lethal arrhythmogenic right ventricular cardiomyopathy type 5 caused by the TMEM43 p.Ser358Leu mutation.

Authors:  Kasper Aalbæk Kjærgaard; Jens Kristensen; Henning Mølgaard; Jens Cosedis Nielsen; Henrik Kjærulf Jensen
Journal:  HeartRhythm Case Rep       Date:  2016-03-04

6.  Incidentally identified genetic variants in arrhythmogenic right ventricular cardiomyopathy-associated genes among children undergoing exome sequencing reflect healthy population variation.

Authors:  Andrew T Headrick; Jill A Rosenfeld; Yaping Yang; Hari Tunuguntla; Hugh D Allen; Daniel J Penny; Jeffrey J Kim; Andrew P Landstrom
Journal:  Mol Genet Genomic Med       Date:  2019-04-15       Impact factor: 2.183

  6 in total

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