Abstract 4368871: Impact of Glucagon-Like Peptide-1 Agonists on Ventricular Tachycardia Ablation Outcomes: a Matched Analysis

A Adele Watfa (Cleveland Clinic, Cleveland, Ohio, United States) C Chadi Tabaja (Cleveland Clinic, Cleveland, Ohio, United States) A Astefanos Al-Dalakta (Cleveland Clinic, Cleveland, Ohio, United States) I Issam Motairek (Cleveland Clinic Foundation, Cleveland, Ohio, United States) M Mohamad Mdaihly (Cleveland Clinic, Cleveland, Ohio, United States) A Arwa Younis (cleveland clinic foundation, Cleveland, Ohio, United States) J Joe Demian (Cleveland Clinic, Cleveland, Ohio, United States) F Fawzi Zghyer (Cleveland Clinic Foundation, Cleveland, Ohio, United States) F Faysal Massad (The Cleveland Clinic Foundation, Cleveland heights, Ohio, United States) J Justin Lee (Department for Biochemistry of Plant Interactions, Leibniz Institute of Plant Biochemistry) M Mohamed Kanj (Cleveland Clinic, Cleveland, Ohio, United States) M Mina Chung (CLEVELAND CLINIC, Cleveland, Ohio, United States) J Jakub Sroubek (Cleveland Clinic, Cleveland, Ohio, United States) W Walid Saliba (CLEVELAND CLINIC, Cleveland, Ohio, United States) A Ayman Hussein (Cleveland Clinic, Cleveland) O Oussama Wazni (Cleveland Clinic, Cleveland, Ohio, United States) P Pasquale Santangeli (Cleveland Clinic, Gates Mills, Ohio, United States)

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

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (17)

A

Adele Watfa

Cleveland Clinic, Cleveland, Ohio, United States

C

Chadi Tabaja

Cleveland Clinic, Cleveland, Ohio, United States

A

Astefanos Al-Dalakta

Cleveland Clinic, Cleveland, Ohio, United States

I

Issam Motairek

Cleveland Clinic Foundation, Cleveland, Ohio, United States

M

Mohamad Mdaihly

Cleveland Clinic, Cleveland, Ohio, United States

A

Arwa Younis

cleveland clinic foundation, Cleveland, Ohio, United States

J

Joe Demian

Cleveland Clinic, Cleveland, Ohio, United States

F

Fawzi Zghyer

Cleveland Clinic Foundation, Cleveland, Ohio, United States

F

Faysal Massad

The Cleveland Clinic Foundation, Cleveland heights, Ohio, United States

J

Justin Lee

Department for Biochemistry of Plant Interactions, Leibniz Institute of Plant Biochemistry

M

Mohamed Kanj

Cleveland Clinic, Cleveland, Ohio, United States

M

Mina Chung

CLEVELAND CLINIC, Cleveland, Ohio, United States

J

Jakub Sroubek

Cleveland Clinic, Cleveland, Ohio, United States

W

Walid Saliba

CLEVELAND CLINIC, Cleveland, Ohio, United States

A

Ayman Hussein

Cleveland Clinic, Cleveland

O

Oussama Wazni

Cleveland Clinic, Cleveland, Ohio, United States

P

Pasquale Santangeli

Cleveland Clinic, Gates Mills, Ohio, United States