Acute post-procedural inducibility is a poor predictor of clinical outcomes in high-risk patients (PAINESD > 17) undergoing scar-related ventricular tachycardia ablation

Author:

Sipko Joseph1ORCID,Baranowski Bryan1,Bhargava Mandeep1,Callahan Thomas D1ORCID,Dresing Thomas J1ORCID,Higuchi Koji1ORCID,Hussein Ayman A1ORCID,Kanj Mohamed1ORCID,Lee Justin1ORCID,Martin David O1,Nakhla Shady1ORCID,Rickard John J1,Saliba Walid I1,Taigen Tyler1ORCID,Wazni Oussama M1,Santangeli Pasquale1ORCID,Sroubek Jakub1ORCID

Affiliation:

1. Section of Cardiac Pacing and Electrophysiology, Cleveland Clinic Foundation , Cleveland, OH , USA

Abstract

Abstract Aims Ventricular tachycardia (VT) non-inducibility in response to programmed ventricular stimulation (PVS) is a widely used procedural endpoint for VT ablation despite inconclusive evidence with respect to clinical outcomes in high-risk patients. The aim is to determine the utility of acute post-ablation VT inducibility as a predictor of VT recurrence, mortality, or mortality equivalent in high-risk patients. Methods and results We conducted a retrospective analysis of high-risk patients (defined as PAINESD > 17) who underwent scar-related VT ablation at our institution between July 2010 and July 2022. Patients’ response to PVS (post-procedure) was categorized into three groups: Group A, no clinical VT or VT with cycle length > 240 ms inducible; Group B, only non-clinical VT with cycle length > 240 ms induced; and Group C, all other outcomes (including cases where no PVS was performed). The combined primary endpoint included death, durable left ventricular assist device placement, and cardiac transplant (Cox analysis). Ventricular tachycardia recurrence was considered a secondary endpoint (competing risk analysis). Of the 1677 VT ablation cases, 123 cases met the inclusion criteria for analysis. During a 19-month median follow-up time (interquartile range 4–43 months), 82 (66.7%) patients experienced the composite primary endpoint. There was no difference between Groups A and C with respect to the primary [hazard ratio (HR) = 1.21 (0.94–1.57), P = 0.145] or secondary [HR = 1.18 (0.91–1.54), P = 0.210] outcomes. These findings persisted after multivariate adjustments. The size of Group B (n = 13) did not permit meaningful statistical analysis. Conclusion The results of post-ablation PVS do not significantly correlate with long-term outcomes in high-risk (PAINESD > 17) VT ablation patients.

Publisher

Oxford University Press (OUP)

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