Literature DB >> 3341180

Critical analysis of cineangiographic criteria for diagnosis of arrhythmogenic right ventricular dysplasia.

C Daubert1, C Descaves, J L Foulgoc, C Bourdonnec, M Laurent, J Gouffault.   

Abstract

Biplane 30-degree RAO and 60-degree LAO RV selective cineangiography was performed in 21 patients with significant ventricular arrhythmias (ventricular tachycardia in 14, salvos in three, and complex PVCs in seven) and a high presumption of arrhythmogenic RV dysplasia (ARVD), and in a control group of 10 presumed normal individuals. Comparing the two series revealed the lack of specificity of some angiographic images usually reported as suggestive signs of ARVD, such as slow dye evacuation of RV during the levophase and deep fissuring in the anterior wall with a "pile of plates" image. Inversely, localized morphologic and contraction abnormalities in the RV free wall were more sensitive and specific signs for diagnosis of ARVD; these were localized akinetic or dyskinetic bulges sometimes giving a true image of aneurysm (90%), wide and deep fissuring of the apex or of the inferior wall (33%), and large areas of akinesia. By order of frequency, these abnormalities were found on the apex in 71%, on the inferior wall in 52%, on the anterior wall in 48%, in the subtricuspid area in 38%, and on the pulmonary infundibulum in 33%. These localized lesions can suffice for the diagnosis of RV dysplasia in the absence of associated pathologies, such as ischemic heart disease or congenital defects. Usually a global RV systolic dysfunction is associated in ARVD, as confirmed by greater RV volumes (134 +/- 26 vs 79 +/- 10 ml/m2 for RVEDV, p less than 0.001; 76 +/- 34 vs 32 +/- 6 ml/m2 for RVESV, p less than 0.001), and lower RV ejection fraction (58 +/- 18% vs 47 +/- 8%, p less than 0.001) in the ARVD group compared to controls. Nevertheless, normal RV volumes and ejection fraction can be observed in some localized forms with mono- or bisegmental lesions in which RV systolic dysfunction is absent or moderate, and extensive forms with multiple segmental lesions where RV systolic dysfunction is constant and often severe. Six out of 21 patients in the ARVD group exhibited obvious global or segmental LV dysfunction, indicating the possibility of biventricular forms, as previously reported in other publications.

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Mesh:

Year:  1988        PMID: 3341180     DOI: 10.1016/0002-8703(88)90494-2

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  10 in total

Review 1.  The arrhythmogenic right ventricle. Dysplasia versus cardiomyopathy.

Authors:  G Fontaine; F Fontaliran; F R Andrade; E Velasquez; J Tonet; X Jouven; Y Fujioka; R Frank
Journal:  Heart Vessels       Date:  1995       Impact factor: 2.037

Review 2.  [Arrhythmogenic right ventricular cardiomyopathy. Etiology, diagnosis and therapy].

Authors:  T Wichter; M Borggrefe; G Breithardt
Journal:  Med Klin (Munich)       Date:  1998-04-15

3.  Spin-echo nuclear magnetic resonance for tissue characterisation in arrhythmogenic right ventricular cardiomyopathy.

Authors:  L Menghetti; C Basso; A Nava; A Angelini; G Thiene
Journal:  Heart       Date:  1996-12       Impact factor: 5.994

4.  Selective right ventricular angiography in apparently idiopathic ventricular fibrillation.

Authors:  S Peters; J Tröster; C A Hartwig; G H Reil
Journal:  Heart Vessels       Date:  1995       Impact factor: 2.037

Review 5.  Arrhythmogenic ventricular cardiomyopathy: A paradigm shift from right to biventricular disease.

Authors:  Ardan M Saguner; Corinna Brunckhorst; Firat Duru
Journal:  World J Cardiol       Date:  2014-04-26

6.  Predictors of adverse outcome in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy: long term experience of a tertiary care centre.

Authors:  K Lemola; C Brunckhorst; U Helfenstein; E Oechslin; R Jenni; F Duru
Journal:  Heart       Date:  2005-09       Impact factor: 5.994

7.  Relative utility of magnetic resonance imaging and right ventricular angiography to diagnose arrhythmogenic right ventricular cardiomyopathy.

Authors:  James B White; Ronald Razmi; Hrudaya Nath; G Neal Kay; Vance J Plumb; Andrew E Epstein
Journal:  J Interv Card Electrophysiol       Date:  2004-02       Impact factor: 1.900

8.  Diagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy. Task Force of the Working Group Myocardial and Pericardial Disease of the European Society of Cardiology and of the Scientific Council on Cardiomyopathies of the International Society and Federation of Cardiology.

Authors:  W J McKenna; G Thiene; A Nava; F Fontaliran; C Blomstrom-Lundqvist; G Fontaine; F Camerini
Journal:  Br Heart J       Date:  1994-03

9.  Right ventricular dysplasia: a clinical and pathological study of two families with left ventricular involvement.

Authors:  D Miani; B Pinamonti; R Bussani; F Silvestri; G Sinagra; F Camerini
Journal:  Br Heart J       Date:  1993-02

10.  Endomyocardial fibrosis with right ventricular aneurysm mimicking ARVC - A case report from India.

Authors:  Suneesh Kalliath; Rajesh Gopalan Nair; Haridasan Vellani
Journal:  Indian Heart J       Date:  2016-08-29
  10 in total

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