Key result
The presence of a single hour with < 50 ventricular ectopics accurately predicted the site of origin in 89.7% of validation patients, yielding a positive predictive value of 95.0%.
Why the study?
Predicting the site of origin of outflow tract ventricular arrhythmia prior to ablation can inform patient consent and procedural planning, but whether arrhythmia variability can accurately predict it remained to be determined.
Does hourly variability in outflow tract ectopy on 24-hour ambulatory ECG accurately predict the site of origin in patients with outflow tract ventricular arrhythmia?
Cohort (n=69)
Does hourly variability in outflow tract ectopy on 24-hour ambulatory ECG accurately predict the site of origin in patients with outflow tract ventricular arrhythmia?
Ventricular ectopic variability and the presence of a single hour with < 50 VE on 24-hour Holter monitoring can accurately predict the site of origin of outflow tract ventricular arrhythmias, performing favorably compared to existing ECG algorithms.
May aid noninvasive localization of outflow tract VA; leaves open prospective validation before clinical adoption.
Introduction: Prior to ablation, predicting the site of origin (SOO) of outflow tract ventricular arrhythmia (OTVA), can inform patient consent and facilitate appropriate procedural planning. We set out to determine if OTVA variability can accurately predict SOO. Methods: Consecutive patients with a clear SOO identified at OTVA ablation had their prior 24-hour ambulatory ECGs retrospectively analysed (derivation cohort). Percentage ventricular ectopic (VE) burden, hourly VE values, episodes of trigeminy/bigeminy, and the variability in these parameters were evaluated for their ability to distinguish right from left sided SOO. Effective parameters were then prospectively tested on a validation cohort of consecutive patients undergoing their first OTVA ablation. Results: High VE variability (coefficient of variation ≥ 0.7) and the presence of any hour with < 50 VE, were found to accurately predict RVOT SOO in a derivation cohort of 40 patients. In a validation cohort of 29 patients, the correct SOO was prospectively identified in 23/29 patients (79.3%) using CoV, and 26/29 patients (89.7%) using VE < 50. Including current ECG algorithms, VE < 50 had the highest Youden Index (78), the highest positive predictive value (95.0%) and the highest negative predictive value (77.8%). Conclusion: VE variability and the presence of a single hour where VE < 50 can be used to accurately predict SOO in patients with OTVA. Accuracy of these parameters compares favourably to existing ECG algorithms.
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Waight et al. (2021) conducted a cohort in Outflow tract ventricular arrhythmia (OTVA) (n=69). Ventricular ectopic (VE) variability and presence of any hour with < 50 VE was evaluated on Correct identification of right ventricular outflow tract (RVOT) site of origin. The presence of a single hour with < 50 ventricular ectopics accurately predicted the site of origin in 89.7% of validation patients, yielding a positive predictive value of 95.0%.
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