Literature DB >> 16253908

Predictors of appropriate implantable defibrillator therapies in patients with arrhythmogenic right ventricular dysplasia.

Jonathan P Piccini1, Darshan Dalal, Ariel Roguin, Chandra Bomma, Alan Cheng, Kalpana Prakasa, Jun Dong, Crystal Tichnell, Cynthia James, Stuart Russell, Jane Crosson, Ronald D Berger, Joseph E Marine, Gordon Tomaselli, Hugh Calkins.   

Abstract

BACKGROUND: Arrhythmogenic right ventricular dysplasia (ARVD) is an inherited cardiomyopathy characterized by ventricular arrhythmias and sudden cardiac death. The risk factors for sudden death and indications for implantable cardioverter-defibrillator (ICD) placement in patients with ARVD are not well defined.
OBJECTIVES: The purpose of this study was to determine which clinical and electrophysiologic variables best predict appropriate ICD therapies in patients with ARVD. Particular attention focused on whether the ICD was implanted for primary or second prevention.
METHODS: We enrolled 67 patients (mean age 36 +/- 14 years) with definite or probable ARVD who had undergone ICD placement. Appropriate ICD therapies were recorded, and Kaplan-Meier analysis was used to compare the event-free survival time between patients based upon the indication for ICD placement (primary vs secondary prevention), results of electrophysiologic testing, and whether the patient had probable or definite ARVD.
RESULTS: Over a mean follow-up of 4.4 +/- 2.9 years, 40 (73%) of 55 patients who met task force criteria for ARVD and 4 (33%) of 12 patients with probable ARVD had appropriate ICD therapies for ventricular tachycardia/ventricular fibrillation (VT/VF; P = .027). Mean time to ICD therapy was 1.1 +/- 1.4 years. Eleven of 28 patients who received an ICD for primary prevention (39%) and 33 of 35 patients who received an ICD for secondary prevention (85%) experienced appropriate ICD therapies (P = .001). Electrophysiologic testing did not predict appropriate ICD interventions in patients who received an ICD for primary prevention. Fourteen patients (21%) received ICD therapy for life-threatening (VT/VF >240 bpm) arrhythmias. There was no difference in the incidence of life-threatening arrhythmias in the primary and secondary prevention groups (P = .29).
CONCLUSION: Patients who meet task force criteria for ARVD are at high risk for sudden cardiac death and should undergo ICD placement for primary and secondary prevention, regardless of electrophysiologic testing results. Further research is needed to confirm that a low-risk subset of patients who may not require ICD placement can be identified.

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Year:  2005        PMID: 16253908     DOI: 10.1016/j.hrthm.2005.08.022

Source DB:  PubMed          Journal:  Heart Rhythm        ISSN: 1547-5271            Impact factor:   6.343


  26 in total

1.  Fontan-like circulation as a criterion for heart transplantation in arrhythmogenic right ventricular dysplasia.

Authors:  Christiana Schernthaner; Gerhard Poelzl; Bernhard Strohmer; Richard Steinacher; Marcel Granitz; Johann Altenberger
Journal:  Wien Klin Wochenschr       Date:  2014-11-15       Impact factor: 1.704

2.  [The ICD as primary prevention. Rare indications].

Authors:  K Wasmer; J Köbe; C Pott; L Eckardt
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2010-06

Review 3.  Arrhythmogenic right ventricular cardiomyopathy/dysplasia: risk stratification and therapy.

Authors:  Gianfranco Buja; N A Mark Estes; Thomas Wichter; Domenico Corrado; Frank Marcus; Gaetano Thiene
Journal:  Prog Cardiovasc Dis       Date:  2008 Jan-Feb       Impact factor: 8.194

Review 4.  Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a not so rare "disease of the desmosome" with multiple clinical presentations.

Authors:  Thomas Herren; Philipp A Gerber; Firat Duru
Journal:  Clin Res Cardiol       Date:  2009-02-09       Impact factor: 5.460

5.  Arrhythmogenic right ventricular cardiomyopathy/dysplasia: an update.

Authors:  Hugh Calkins; Frank Marcus
Journal:  Curr Cardiol Rep       Date:  2008-09       Impact factor: 2.931

Review 6.  Clinical screening and genetic testing.

Authors:  Rahul C Deo; Calum A MacRae
Journal:  Heart Fail Clin       Date:  2010-04       Impact factor: 3.179

Review 7.  Advances in the Diagnosis and Management of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy.

Authors:  Gabriela M Orgeron; Hugh Calkins
Journal:  Curr Cardiol Rep       Date:  2016-06       Impact factor: 2.931

Review 8.  Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C): a review of molecular and clinical literature.

Authors:  Brittney Murray
Journal:  J Genet Couns       Date:  2012-03-17       Impact factor: 2.537

Review 9.  Arrhythmogenic right ventricular cardiomyopathy/dysplasia: a review and update.

Authors:  A Azaouagh; S Churzidse; T Konorza; R Erbel
Journal:  Clin Res Cardiol       Date:  2011-03-01       Impact factor: 5.460

10.  Arrhythmogenic right ventricular dysplasia.

Authors:  Hugh Calkins
Journal:  Trans Am Clin Climatol Assoc       Date:  2008
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