Abstract 4368871: Impact of Glucagon-Like Peptide-1 Agonists on Ventricular Tachycardia Ablation Outcomes: a Matched Analysis
Abstract
Background: Glucagon-like peptide-1 receptor agonists (GLP-1 RA) have been shown to reduce major cardiac events. However, their impact on ventricular tachycardia (VT) catheter ablation outcomes is not well studied. Aims: To examine the impact of GLP-1 RA use on VT ablation outcomes. Methods: Using the TriNetX research network we identified, by means of Current Procedural Terminology codes, patients ≥18 years of age who had undergone VT ablation between 2010 and 2024. Patients undergoing premature ventricular ablation were excluded. Patients were stratified based on the baseline GLP-1 RA use at the time of index procedure. The primary outcome was in-hospital mortality. Secondary outcomes were VT recurrence, repeat ablation, cardiac tamponade and need for blood transfusion. Results: Propensity-score matching resulted in 584 patients in each cohort. The mean age was 63 ± 810 years and 70% were males. GLP-1 RA use was associated with a significantly lower risk of in-hospital mortality (HR 0.51; 95% CI 0.38–0.67; p = 0.005), VT recurrence (HR 0.82; 95% CI 0.69–0.96; p = 0.04), repeat ablation (HR 0.627; 95% CI 0.40–0.96; p = 0.031), and need for blood transfusion (HR 0.45; 95% CI 0.28–0.71; p < 0.001). No significant difference was observed in the risk of cardiac tamponade (HR 0.753; 95% CI 0.17–3.37; p = 0.39). Conclusion: In this large, real-world cohort of patients undergoing catheter ablation for VT, baseline use of GLP-1 RA use was independently associated with lower risks of mortality, arrhythmia recurrence, repeat ablation, and transfusions. No significant difference was observed in procedural complication rates. These findings generate hypothesis-supporting evidence for a potential protective role of GLP-1 RAs in the VT ablation population and highlight the need for prospective studies to validate their mechanistic and therapeutic impact on ventricular arrythmias.
Article Details
Authors (17)
Adele Watfa
Cleveland Clinic, Cleveland, Ohio, United States
Chadi Tabaja
Cleveland Clinic, Cleveland, Ohio, United States
Astefanos Al-Dalakta
Cleveland Clinic, Cleveland, Ohio, United States
Issam Motairek
Cleveland Clinic Foundation, Cleveland, Ohio, United States
Mohamad Mdaihly
Cleveland Clinic, Cleveland, Ohio, United States
Arwa Younis
cleveland clinic foundation, Cleveland, Ohio, United States
Joe Demian
Cleveland Clinic, Cleveland, Ohio, United States
Fawzi Zghyer
Cleveland Clinic Foundation, Cleveland, Ohio, United States
Faysal Massad
The Cleveland Clinic Foundation, Cleveland heights, Ohio, United States
Justin Lee
Department for Biochemistry of Plant Interactions, Leibniz Institute of Plant Biochemistry
Mohamed Kanj
Cleveland Clinic, Cleveland, Ohio, United States
Mina Chung
CLEVELAND CLINIC, Cleveland, Ohio, United States
Jakub Sroubek
Cleveland Clinic, Cleveland, Ohio, United States
Walid Saliba
CLEVELAND CLINIC, Cleveland, Ohio, United States
Ayman Hussein
Cleveland Clinic, Cleveland
Oussama Wazni
Cleveland Clinic, Cleveland, Ohio, United States
Pasquale Santangeli
Cleveland Clinic, Gates Mills, Ohio, United States