Two-to-one AV block associated with the congenital long QT syndrome

Détails

ID Serval
serval:BIB_A9C085626DCA
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Etude de cas (case report): rapporte une observation et la commente brièvement.
Collection
Publications
Institution
Titre
Two-to-one AV block associated with the congenital long QT syndrome
Périodique
Journal of Cardiovascular Electrophysiology
Auteur⸱e⸱s
Pruvot  E., De Torrente  A., De Ferrari  G. M., Schwartz  P. J., Goy  J. J.
ISSN
1045-3873 (Print)
Statut éditorial
Publié
Date de publication
01/1999
Volume
10
Numéro
1
Pages
108-13
Notes
Case Reports
Journal Article --- Old month value: Jan
Résumé
INTRODUCTION: Conduction abnormalities associated with long QT syndrome (LQTS) have been reported as "pseudo 2:1 AV block" due to sinus intervals shorter than ventricular refractoriness. METHOD AND RESULTS: We report the electrophysiologic characteristics of a patient suffering from congenital LQTS with episodes of true 2:1 AV block. Induction of 2:1 infra-Hisian blocks and return to 1:1 conduction were observed using single atrial and ventricular extrastimuli. The block was located in the Purkinje network but not in the myocardium. CONCLUSION: The His-Purkinje system of our LQTS patient displayed dynamic properties with a strong increase in refractoriness for short-long sequences and a decrease for long-short sequences that triggered intermittent 2:1 AV blocks.
Mots-clé
Adolescent Cardiac Pacing, Artificial *Electrocardiography Female Follow-Up Studies Heart Block/*etiology/physiopathology/therapy Humans Long QT Syndrome/complications/*congenital/physiopathology Purkinje Fibers/physiopathology Sympathectomy
Pubmed
Web of science
Création de la notice
28/01/2008 11:04
Dernière modification de la notice
20/08/2019 16:13
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