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Wolff-Parkinson-White syndrome

Identifieur interne : 000134 ( Main/Corpus ); précédent : 000133; suivant : 000135

Wolff-Parkinson-White syndrome

Auteurs : Andrew G. Wallace ; John P. Boineau ; Robert M. Davidson ; Will C. Sealy

Source :

RBID : ISTEX:7715B38D1492FDC0A00D811C31786015306DF2F1

Abstract

In the past 4 years physiologic studies of patients with the Wolff-Parkinson-White (WPW) syndrome and its variants have shed new light on the structural basis for this electrocardiographic abnormality and the mechanisms responsible for supraventricular arrhythmias. Accessory pathways for atrioventricular propagation appear to be responsible for the electrocardiographic abnormality in the majority of the patients with this syndrome. These pathways may be similar to those described by Kent and located in the lateral portion of either the right or left atrioventricular groove, or the accessory bundles bypassing the atrioventricular node may be located within the septal region. Careful analysis of the electrocardiogram, atrial pacing studies and the records from the bundle of His can be used to identify the probable location of the pathway as well as certain of its functional characteristics. Surgical interruption of the accessory pathway provides a definitive form of therapy, although this approach is not necessary in the majority of patients with WPW syndrome. Furthermore, surgical intervention should be entertained only after physiologic studies have been made and in a setting in which careful epicardial mapping can be performed at the time of surgical intervention.

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DOI: 10.1016/0002-9149(71)90092-0

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ISTEX:7715B38D1492FDC0A00D811C31786015306DF2F1

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