Literature DB >> 8172478

[Repolarization and intraventricular conduction disorders in arrhythmogenic right ventricular dysplasia].

G Fontaine1, R Tsezana, A Lazarus, G Lascault, J Tonet, R Frank.   

Abstract

Right ventricular dysplasia may lead to sudden cardiac death an adolescent or adult with little or no symptoms. Identification of this condition in the high-risk population appears to be an objective to be attained in the near future. Thorough ECG analysis seems to be a non-invasive and inexpensive technique which could be used as a first approach for screening of the disorder. In a series of 50 cases of arrhythmogenic right ventricular dysplasia compared with a control group, the diagnosis of ARVD could be determined by ECG with 84% sensitivity and 100% specificity if QRS duration in leads V1, V2 or V3 was longer than 110 ms, T wave was negative in V2 or if T wave was negative in V1, but in this latter case only provided incomplete right bundle branch block was present.

Entities:  

Mesh:

Year:  1994        PMID: 8172478

Source DB:  PubMed          Journal:  Ann Cardiol Angeiol (Paris)        ISSN: 0003-3928


  2 in total

1.  Electrocardiographic and morphometric features in patients with ventricular tachycardia of right ventricular origin.

Authors:  J Kazmierczak; J De Sutter; R Tavernier; C Cuvelier; C Dimmer; L Jordaens
Journal:  Heart       Date:  1998-04       Impact factor: 5.994

2.  Right-ventricular enlargement in arrhythmogenic right-ventricular cardiomyopathy is associated with decreased QRS amplitudes and T-wave negativity.

Authors:  Robbert Zusterzeel; Rachel M A Ter Bekke; Paul G A Volders; Farah M M Leijten; Arthur van den Wijngaard; Jan Serroyen; Anton P M Gorgels
Journal:  Ann Noninvasive Electrocardiol       Date:  2013-09-09       Impact factor: 1.468

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.