Literature DB >> 1693199

Persistent functional atrioventricular block in two patients with prolonged QT intervals: elucidation of the mechanism of block.

G F van Hare1, M R Franz, C Rogé, M M Scheinman.   

Abstract

This article describes two infants with prolonged QT interval and intermittent second-degree atrioventricular block. An asymptomatic 14-month-old child with persistent 2:1 atrioventricular conduction since birth underwent electrophysiology study including measurements with a contact monophasic action potential catheter. During 2:1 conduction, atrioventricular block occurred distal to the site of the His-bundle recording. Monophasic action potential duration was closely related to prior RR intervals. Single premature atrial or ventricular depolarizations during 1:1 conduction followed by a pause, lead to monophasic action potential prolongation and subsequent 2:1 atrioventricular conduction, which was perpetuated by the resulting long RR intervals. Paired premature ventricular contractions or short bursts of ventricular pacing elicited monophasic action potential shortening and subsequent 1:1 atrioventricular conduction that was perpetuated by the resulting short RR intervals. A second infant presented at birth with a prolonged QT interval, ventricular tachycardia, and episodes of second-degree atrioventricular block with persistent 2:1 atrioventricular conduction. The atrioventricular block was repeatedly elicited by single premature ventricular contractions and terminated by ventricular couplets. We conclude that the atrioventricular block in both patients is functional in nature and results from the interrelationships between ventricular rate, action potential duration, and His-Purkinje system refractoriness.

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Year:  1990        PMID: 1693199     DOI: 10.1111/j.1540-8159.1990.tb02077.x

Source DB:  PubMed          Journal:  Pacing Clin Electrophysiol        ISSN: 0147-8389            Impact factor:   1.976


  6 in total

1.  Survival of a Newborn with 2:1 Atrioventricular Block, Long QT Syndrome, and Torsades de Pointes.

Authors:  Shubho Sarkar; Michael Brumund; Rani Darling; Christopher S Snyder
Journal:  Ochsner J       Date:  2007

Review 2.  Arrhythmias in the congenital long QT syndrome: how often is torsade de pointes pause dependent?

Authors:  S Viskin; R Fish; D Zeltser; B Belhassen; K Heller; D Brosh; S Laniado; H V Barron
Journal:  Heart       Date:  2000-06       Impact factor: 5.994

3.  Prenatal findings in patients with prolonged QT interval in the neonatal period.

Authors:  M Hofbeck; H Ulmer; E Beinder; E Sieber; H Singer
Journal:  Heart       Date:  1997-03       Impact factor: 5.994

4.  Autonomic modulation and antiarrhythmic therapy in a model of long QT syndrome type 3.

Authors:  Larissa Fabritz; Dierk Damke; Markus Emmerich; Susann G Kaufmann; Kathrin Theis; Andreas Blana; Lisa Fortmüller; Sandra Laakmann; Sven Hermann; Elena Aleynichenko; Johannes Steinfurt; Daniela Volkery; Burkhard Riemann; Uwe Kirchhefer; Michael R Franz; Günter Breithardt; Edward Carmeliet; Michael Schäfers; Sebastian K G Maier; Peter Carmeliet; Paulus Kirchhof
Journal:  Cardiovasc Res       Date:  2010-01-28       Impact factor: 10.787

5.  Long QT syndrome and life threatening arrhythmia in a newborn: molecular diagnosis and treatment response.

Authors:  E Schulze-Bahr; H Fenge; D Etzrodt; W Haverkamp; G Mönnig; H Wedekind; G Breithardt; H-G Kehl
Journal:  Heart       Date:  2004-01       Impact factor: 5.994

6.  SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome.

Authors:  Argelia Medeiros-Domingo; Toshihiko Kaku; David J Tester; Pedro Iturralde-Torres; Ajit Itty; Bin Ye; Carmen Valdivia; Kazuo Ueda; Samuel Canizales-Quinteros; Maria Teresa Tusié-Luna; Jonathan C Makielski; Michael J Ackerman
Journal:  Circulation       Date:  2007-06-25       Impact factor: 29.690

  6 in total

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