Evaluation of T‐wave memory after accessory pathway ablation in pediatric patients with Wolff‐Parkinson‐White syndrome

Abstract Background T‐wave memory (TWM) is a rare cause of T‐wave inversion (TWI). Alterations in ventricular activation due to abnormal depolarization may cause repolarization abnormalities on the ECG, even if myocardial conduction returns to normal. These repolarization changes are defined as TWM. In our study, we aimed to determine the frequency of TWM development and the predictors affecting it in the pediatric population who underwent accessory pathway (AP) ablation due to Wolff‐Parkinson‐White (WPW) syndrome. Methods The data of patients with manifest AP who underwent electrophysiological studies and ablation between 2015 and 2021 were retrospectively analyzed. The study included 180 patients who were under 21 years of age and had at least one year of follow‐up after ablation. Patients with structural heart disease, intermittent WPWs, recurrent ablation, other arrhythmia substrates, and those with less than one‐year follow‐up were excluded from the study. The ECG data of the patients before the procedure, in the first 24 h after the procedure, three months, and in the first year were recorded. The standard ablation technique was used in all patients. Results Postprocedure TWM was observed in 116 (64.4%) patients. Ninety‐three patients (51.7%) had a right‐sided AP, and 87 patients (48.3%) had a left‐sided AP. The presence of posteroseptal AP was found to be significantly higher in the group that developed TWM. Of these patients, 107 (93.1%) patients showed improvement at the end of the first year. Preprocedural absolute QRS‐T angle, postprocedural PR interval, and right posteroseptal pathway location were identified as predictors of TWM. Conclusion The development of TWM is particularly associated with the right‐sided pathway location, especially the right posteroseptal pathway location. The predictors of TWM are the preprocedural QRS‐T angle, the postprocedural PR interval, and the presence of the right posteroseptal AP.