Why the study?
Can ECG imaging (ECGI) noninvasively localize accessory pathways and characterize the time course of cardiac memory (ARI dispersion) after ablation in pediatric patients with Wolff-Parkinson-White syndrome?
Can ECG imaging (ECGI) noninvasively localize accessory pathways and characterize the time course of cardiac memory (ARI dispersion) after ablation in pediatric patients with Wolff-Parkinson-White syndrome?
ECGI can noninvasively map cardiac memory in WPW syndrome, demonstrating that repolarization abnormalities persist for up to a month after successful ablation.
Should not yet change post-ablation care in pediatric WPW; hypothesis-generating for ECGI in cardiac memory assessment.
BACKGROUND: Cardiac memory refers to a change in ventricular repolarization induced by and persisting for minutes to months after cessation of a period of altered ventricular activation (eg, resulting from pacing or preexcitation in patients with Wolff-Parkinson-White syndrome). ECG imaging (ECGI) is a novel imaging modality for noninvasive electroanatomic mapping of epicardial activation and repolarization. METHODS AND RESULTS: Fourteen pediatric patients with Wolff-Parkinson-White syndrome and no other congenital disease, were imaged with ECGI a day before and 45 minutes, 1 week, and 1 month after successful catheter ablation. ECGI determined that preexcitation sites were consistent with sites of successful ablation in all cases to within a 1-hour arc of each atrioventricular annulus. In the preexcited rhythm, activation-recovery interval (ARI) was the longest (349+/-6 ms) in the area of preexcitation leading to high average base-to-apex ARI dispersion of 95+/-9 ms (normal is approximately 40 ms). The ARI dispersion remained the same 45 minutes after ablation, although the activation sequence was restored to normal. ARI dispersion was still high (79+/-9 ms) 1 week later and returned to normal (45+/-6 ms) 1 month after ablation. CONCLUSIONS: The study demonstrates that ECGI can noninvasively localize ventricular insertion sites of accessory pathways to guide ablation and evaluate its outcome in pediatric patients with Wolff-Parkinson-White syndrome. Wolff-Parkinson-White is associated with high ARI dispersion in the preexcited rhythm that persists after ablation and gradually returns to normal over a period of 1 month, demonstrating the presence of cardiac memory. The 1-month time course is consistent with transcriptional reprogramming and remodeling of ion channels.
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Ghosh et al. (2008) studied this question.
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