Key result
Prolonged Tp-e interval identifies pediatric myocarditis with ~0.73 AUC and flags ventricular arrhythmia risk.
Why the study?
Paediatric myocarditis challenges emergency diagnosis due to nonspecific symptoms mimicking common illnesses, prompting evaluation of electrocardiographic markers of ventricular repolarisation heterogeneity for diagnosing myocarditis and predicting ventricular arrhythmia risk in children.
Do electrocardiographic markers of ventricular repolarisation heterogeneity (T-peak to T-end, T peak-to-end/corrected QT ratio, and index of cardiac electrophysiological balance) accurately diagnose myocarditis and predict ventricular arrhythmia risk in children aged 0-18 years?
Case-Control (n=151)
No
Do electrocardiographic markers of ventricular repolarisation heterogeneity (T-peak to T-end, T peak-to-end/corrected QT ratio, and index of cardiac electrophysiological balance) accurately diagnose myocarditis and predict ventricular arrhythmia risk in children aged 0-18 years?
T-peak to T-end interval, T peak-to-end/QTc ratio, and index of cardiac electrophysiological balance offer high-specificity, noninvasive ECG biomarkers to aid in the emergency diagnosis and arrhythmia risk stratification of paediatric myocarditis.
Answers are grounded in this paper and cite their sources.
T-peak to T-end interval may aid paediatric myocarditis diagnosis; hypothesis-generating for arrhythmia risk stratification pending prospective validation.
Aim: Paediatric myocarditis, a rare inflammatory cardiomyopathy (incidence 1–2/100,000 annually), challenges emergency diagnosis due to nonspecific symptoms mimicking common illnesses. This study assessed electrocardiographic markers of ventricular repolarisation heterogeneity—T-peak to T-end interval, T-peak to T-end/QT, T peak–to–end/corrected QT ratios, and index of cardiac electrophysiological balance—for diagnosing myocarditis and predicting ventricular arrhythmia risk in children aged 0–18 years. Methods: Retrospective case–control study of 76 myocarditis patients (diagnosed by clinical, laboratory, echocardiographic, and cardiac MRI criteria) presenting to our paediatric emergency department from January 1, 2024, to May 30, 2025, versus 75 age-matched healthy controls. Electrocardiographic parameters were measured in leads DII and V5. Receiver operating characteristic analysis evaluated the diagnostic performance of T-peak to T-end and T peak–to–end/corrected QT (Lead II (Derivation II)). Myocarditis cases stratified by arrhythmia development (with: n = 28; without: n = 48); groups compared via t -tests, Mann–Whitney U , and chi-square ( p < 0.05 significant). Results: Myocarditis group: 23 females (30.2%) and 53 males (69.8%); mean age 12.0 ± 4.7 years. Controls: 39 females (52.0%), 36 males (48.0%); mean age 10.3 ± 4.9 years ( p = 0.03). Receiver operating characteristic (Lead II (Derivation II)): T-peak to T-end cut-off 62 ms (sensitivity 69.3%, specificity 78.9%, area under the curve 0.725, p < 0.001); T peak–to–end/corrected QT cut-off 0.19 (sensitivity 50.7%, specificity 78.9%, area under the curve 0.625, p < 0.05). The arrhythmia subgroup showed corrected QT prolongation (470 vs. 435 ms, V5; p < 0.001), T-peak to T-end (110 vs. 90 ms, V5; p < 0.001), higher T peak–to–end/corrected QT, and index of cardiac electrophysiological balance (both p < 0.05). Conclusion: The T-peak to T-end interval, T peak–to–end/corrected QT ratio, and index of cardiac electrophysiological balance provide high-specificity, noninvasive electrocardiographic biomarkers for paediatric myocarditis diagnosis in the ED. Corrected QT and T-peak to T-end prolongation signals repolarisation heterogeneity and arrhythmia risk, supporting routine triage integration for early risk stratification.
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Tanyeli et al. (2026) conducted a case-control in Paediatric myocarditis (n=151). ECG markers of ventricular repolarisation heterogeneity (T-peak to T-end interval, T-peak to T-end/QT, T peak-to-end/QTc ratios, and index of cardiac electrophysiological balance) vs. Age-matched healthy controls (n=75); myocarditis patients without arrhythmia (n=48) was evaluated on Differential diagnosis of paediatric myocarditis and prediction of ventricular arrhythmia risk (AUC 0.725, p=<0.001). T-peak to T-end interval (cut-off 62 ms) identified paediatric myocarditis with 69.3% sensitivity and 78.9% specificity (AUC 0.725, p<0.001) and was prolonged in arrhythmia cases (110 vs 90 ms, p<0.001).
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