Abstract 4369080: Catheter ablation of epicardial premature ventricular complexes in patients with and without cardiac scar

S Sania Jiwani (University of Michigan, Ann Arbor, Michigan, United States) M Muazzum Shah (University of Michigan, Ann Arbor, Michigan, United States) K Kelly Arps (University of Michigan, Ann Arbor, Michigan, United States) A Amrish Deshmukh (University of Michigan, Ann Arbor, Michigan, United States) J Jackson Liang R Rakesh Latchamsetty (University of Michigan, Ann Arbor, Michigan, United States) T Thomas Crawford (University of Michigan, Ann Arbor, Michigan, United States) K Krit Jongnarangsin (University Michigan Health System, Ann Arbor, Michigan, United States) H Hakan Oral (University of Michigan, Ann Arbor, Michigan, United States) F Frank Bogun (University of Michigan, Ann Arbor, Michigan, United States) M Michael Ghannam (University of Michigan, Ann Arbor, Michigan, United States)

Abstract

Background: The left ventricular epicardium is a common site of origin (SOO) among patients with idiopathic premature ventricular complexes (PVCs) undergoing catheter ablation procedures. Less is known about epicardial PVC ablation among patients with structural heart disease and cardiac scar. Objective: To report on the presence and impact of cardiac scar among patients with epicardial PVCs undergoing ablation procedures. Methods: In a retrospective analysis, patients with epicardial PVCs and delayed enhancement cardiac magnetic resonance imaging were included. Acute and long-term procedural outcomes were examined and stratified by the presence or absence of cardiac scar. Results: Twenty-nine patients were included (male 17/29(59%), age 55±14years, ejection fraction 48±12%, PVC burden 25±12%, ischemic cardiomyopathy (CM) n=3, non-ischemic CM n=7, PVC induced CM n=5). The SOO was left ventricular summit (n=20), great cardiac vein (n=2), cardiac crux (n=4), or basal anterolateral epicardium (n=3). Ablation within the CVS was limited by proximity to the coronary arteries (n=16), inaccessibility of ablation catheter (n=5), or elevated baseline impedance (n=2). LGE-CMR scar was present at the arrhythmia SOO in 14/29(48%) patients. LGE-CMR was detected in 4/15 (27%) patients with normal ejection fraction and no previously known structural heart disease. There were no differences in procedural, radiofrequency, or fluoroscopy times between patients with and without scar (p>0.05). Ablation was successful in 20/29(69%) patients, the post-ablation PVC burden was 8±6% with no differences among those with or without cardiac scar (P>0.05). Conclusion: Epicardial PVCs may be encountered in patients with and without structural heart disease, with LGE-CMR located at the PVC SOO in 48% of patients. Routine LGE-CMR detected cardiac scar in 27% of patients with epicardial PVCs and no previously known structural heart disease. Ablation is frequently limited by the proximity of the coronary arteries to the PVC SOO and challenges navigating within the CVS. Mapping and ablation in multiple cardiac chambers is often required to attain procedural success.

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 (11)

S

Sania Jiwani

University of Michigan, Ann Arbor, Michigan, United States

M

Muazzum Shah

University of Michigan, Ann Arbor, Michigan, United States

K

Kelly Arps

University of Michigan, Ann Arbor, Michigan, United States

A

Amrish Deshmukh

University of Michigan, Ann Arbor, Michigan, United States

J

Jackson Liang

R

Rakesh Latchamsetty

University of Michigan, Ann Arbor, Michigan, United States

T

Thomas Crawford

University of Michigan, Ann Arbor, Michigan, United States

K

Krit Jongnarangsin

University Michigan Health System, Ann Arbor, Michigan, United States

H

Hakan Oral

University of Michigan, Ann Arbor, Michigan, United States

F

Frank Bogun

University of Michigan, Ann Arbor, Michigan, United States

M

Michael Ghannam

University of Michigan, Ann Arbor, Michigan, United States