EVOLUTION OF THE WOLFF-PARKINSON-WHITE SY NDROME IN CHILDHOOD - TRANSESOPHAGEAL RECORDINGS OF ANTEROGRADE-CONDUCTION OF THE ACCESSORY PATHWAY AND OF ATRIAL VULNERABILITY
E. Villain et al., EVOLUTION OF THE WOLFF-PARKINSON-WHITE SY NDROME IN CHILDHOOD - TRANSESOPHAGEAL RECORDINGS OF ANTEROGRADE-CONDUCTION OF THE ACCESSORY PATHWAY AND OF ATRIAL VULNERABILITY, Archives des maladies du coeur et des vaisseaux, 87(5), 1994, pp. 649-652
Twenty-nine children with the Wolff-Parkinson-White syndrome (WPW) wer
e evaluated by transoesophageal electrophysiological studies to determ
ine the quality of anterograde conduction in the accessory pathway and
the atrial vulnerability. The study group included 15 neonates, 1 to
30 days old, and 14 children from 5 to 15 years of age; Anterograde co
nduction through the bundle of Kent was tested by incremental transoes
ophageal atrial pacing and by the determination of the shortest conduc
ted cycle with preexcited RR waves: bursts of atrial pacing were then
used to try to trigger an atrial arrhythmia. In the group of the 15 ne
onates, 11 had accessory pathways capable of conduction to the ventric
ules at frequencies > 300/min (stimulation cycle less-than-or-equal-to
2,00 ms) but no atrial arrhythmias could be induced. The older childr
en had slower conduction in the accessory pathways with the shortest c
onducted cycle lenght > 200 ms in 11/14 cases; on the other hand, atri
al fibrillation was easily induced in 4 children, all over 12 years of
age. The risk of syncope by rapid conduction of an atrial arrhythmia
through the accessory pathway is negligeable in young children, includ
ing those on digoxin. This study suggests that this low risk is explai
ned more by the absence of atrial vulnerability than by the electrophy
siological properties of the accessory pathways.