Loading…

Paroxysmal atrioventricular block: Electrophysiological mechanism of phase 4 conduction block in the His‐Purkinje system: A comparison with phase 3 block

Background Paroxysmal atrioventricular (A‐V) block is relatively rare, and due to its transient nature, it is often under recognized. It is often triggered by atrial, junctional, or ventricular premature beats, and occurs in the presence of a diseased His‐Purkinje system (HPS). Here, we present a 45...

Full description

Saved in:
Bibliographic Details
Published in:Pacing and clinical electrophysiology 2017-11, Vol.40 (11), p.1234-1241
Main Authors: Shenasa, Mohammad, Josephson, Mark E., Wit, Andrew L.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Background Paroxysmal atrioventricular (A‐V) block is relatively rare, and due to its transient nature, it is often under recognized. It is often triggered by atrial, junctional, or ventricular premature beats, and occurs in the presence of a diseased His‐Purkinje system (HPS). Here, we present a 45‐year‐old white male who was admitted for observation due to recurrent syncope and near‐syncope, who had paroxysmal A‐V block. The likely cellular electrophysiological mechanisms(s) of paroxysmal A‐V block and its differential diagnosis and management are discussed. Methods Continuous electrocardiographic monitoring was done while the patient was in the cardiac unit. Results Multiple episodes of paroxysmal A‐V block were documented in this case. All episodes were initiated and terminated with atrial/junctional premature beats. The patient underwent permanent pacemaker implantation and has remained asymptomatic since then. Conclusions Paroxysmal A‐V block is rare and often causes syncope or near‐syncope. Permanent pacemaker implantation is indicated according to the current guidelines. Paroxysmal A‐V block occurs in the setting of diseased HPS and is bradycardia‐dependent. The detailed electrophysiological mechanisms, which involve phase 4 diastolic depolarization, and differential diagnosis are discussed.
ISSN:0147-8389
1540-8159
DOI:10.1111/pace.13187