Key result
VISTA clinical models predict 24-month mortality and arrhythmic recurrence following VT ablation.
Why the study?
Can the VISTA-R and VISTA-M scores accurately predict 24-month arrhythmic recurrence and mortality following VT ablation in patients with structural heart disease?
Cohort
No
Can the VISTA-R and VISTA-M scores accurately predict 24-month arrhythmic recurrence and mortality following VT ablation in patients with structural heart disease?
Effect estimate: AUC 0.826 (VISTA-M) and AUC 0.63 (VISTA-R)
The novel VISTA-M and VISTA-R scores provide clinically applicable tools for risk stratification of mortality and arrhythmic recurrence at 24 months following VT ablation in patients with structural heart disease.
May aid post-VT ablation risk stratification; leaves open prospective validation before clinical use.
Background/Objectives: Scar-related ventricular tachycardia (VT) remains a major contributor to morbidity and mortality in patients with structural heart disease (SHD), despite advances in catheter ablation (CA). Existing risk scores are limited by their focus on procedural outcomes, restricted variable sets, and insufficient integration of arrhythmic burden. This study aimed to bridge this gap in evidence and develop and internally validate two novel, clinically applicable prediction models—the VISTA-R and VISTA-M scores—for estimating the risk of 24-month arrhythmic recurrence and mortality following VT ablation. Methods: We analyzed a retrospective, single-center cohort of consecutive patients undergoing radiofrequency catheter ablation (RFCA) for scar-related VT in the setting of SHD and included a comprehensive set of clinical, arrhythmic, device-related, and procedural variables. Candidate predictors were identified through univariate logistic regression and subsequently incorporated into an exhaustive combinatorial modeling framework, generating over 1000 candidate models per endpoint. Final model selection was based on discrimination, calibration, and clinical interpretability. Internal validation was performed using leave-one-out cross-validation. Results: The VISTA-M model, incorporating left ventricular ejection fraction (LVEF), NYHA class IV at admission, number of clinical VT morphologies, and appropriate implantable-cardioverter defibrillator (ICD) shocks, demonstrated strong discriminative performance (AUC 0.866 in-sample, 0.826 cross-validated) and a pseudo R2 of approximately 30%. The VISTA-R model, including history of electrical storm (ES), ICD shocks, and VT morphologies, showed moderate discrimination (AUC 0.70 in-sample, 0.63 cross-validated) with a pseudo R2 of approximately 12%. Both models enabled meaningful risk stratification with progressively increasing event rates across the predefined risk classes. Conclusions: In conclusion, the VISTA scores provide parsimonious and clinically applicable tools for a comprehensive risk stratification after VT RFCA. Mortality is primarily driven by myocardial dysfunction and heart failure severity, whereas recurrence reflects arrhythmic burden and electrical instability. External validation is warranted to confirm these findings.
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Stanciulescu et al. (2026) conducted a cohort in Scar-related ventricular tachycardia in structural heart disease. VISTA-M and VISTA-R clinical prediction models was evaluated on 24-month arrhythmic recurrence and mortality (AUC 0.826 (VISTA-M) and AUC 0.63 (VISTA-R)). The VISTA-M and VISTA-R clinical models predicted 24-month mortality (cross-validated AUC 0.826) and arrhythmic recurrence (cross-validated AUC 0.63) following ventricular tachycardia ablation.
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