Abstract 4339399: Incidence and predictors of Monomorphic Ventricular Tachycardia in Three Major Subcutaneous ICD Trials

P Pier Lambiase (Heart Hospital, UCL, London, United Kingdom) M Michael Gold (MEDICAL UNIVERSITY SOUTH CAROLINA, Charleston, South Carolina, United States) U Ulrika Birgersdotter-Green (US San Diego Health, San Deigo, California, United States) L Lars Eckardt (University of Munster, Munster, Germany) B Bradley Knight (Northwestern University, Chicago, Illinois, United States) R Reinoud Knops (Amsterdam University Medical Center, Amsterdam, Netherlands) C Christelle Marquie (Department of Cardiology, University Hospital of Lille, Lille, France (C.M.).) S Stefano Viani (University Hospital of Pisa, Pisa, Italy) L Lucas Boersma (St.Antonius Hospital, Nieuwegein, Netherlands) A Amy Brisben (Boston Scientific, St. Paul, Minnesota, United States) M Madelyn Duffy (Boston Scientific, St. Paul, Minnesota, United States) M Mikhael El-Chami (Emory University School of Medicine, Atlanta, Georgia, United States) A Andrea Russo

Abstract

Background: The subcutaneous ICD (S-ICD) is currently contraindicated for patients (pts) who have monomorphic ventricular tachycardia (MVT) that can be terminated by anti-tachycardia pacing (ATP). Discriminating S-ICD pts who subsequently present with MVT can help identify those who would benefit from a transvenous ICD or upgrade to an investigational, modular leadless pacemaker/S-ICD system to deliver anti-tachycardia pacing. Objective: Identification of burden and determinants of MVT in S-ICD recipients. Methods: Pooled data from 3 S-ICD studies: EFFORTLESS (N=994), S-ICD PAS (N=1643), and UNTOUCHED (N=1116) were analyzed. All MVT episodes of all cycle lengths (treated with ≥1 shock and untreated: self-terminated or rate<programming prior to shock) were considered. Predictors of MVT were identified using stepwise selection (α=20). Kaplan-Meier analysis was employed to assess MVT risk by significant predictors. Results: A total of 3753 pts was followed for 3.6 years (median). Of these, 549 (14.6%) experienced >1 MVT episode (table). Age was 54±15 years, 80% male, 77% primary prevention, and EF 32±15%. Of these 549 pts, 373 pts experienced ≥2 episodes, with median time between 1 st and 2 nd episode 102 (interquartile range 6,391) days. The 5-year rate of experiencing MVT was 20% with shock therapy in 11% (fig1). A total of 298 pts (7.9%) experienced ≥1 shock in 804 episodes, 7% pts had ≥1 shocks for fast MVT (>200bpm), and 52 pts (1.4%) experienced 67 storms (≥3 episodes/24 hours). S-ICD extraction due to the need for ATP pacing was reported for only 10 (0.3%) patients While several baseline variables were identified as a risk of MVT, the multivariable predictor model indicated that pts who experienced MVT were more likely to have a lower ejection fraction and less likely to have diabetes (fig2). Risk of MVT across EF quartiles differed by ≤4.1% with EF 30-35% having the most events and presence of diabetes differed by ≤2.1%, respectively, across all time points. Conclusions: Over 5 years, 11% of S-ICD patients from EFFORTLESS, S-ICD PAS, and UNTOUCHED studies experienced shock therapy for MVTs, and 20% of patients had MVT (treated and untreated). Conversion rate to TV-ICD for ATP was low. Surprisingly, many of the expected risk factors for MVT were not predictive of MVT, which may be in part due to proper exclusion of patients with a MVT in S-ICD studies. Further detailed analysis of univariable predictor and MVT features could help inform device prescription.

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 (13)

P

Pier Lambiase

Heart Hospital, UCL, London, United Kingdom

M

Michael Gold

MEDICAL UNIVERSITY SOUTH CAROLINA, Charleston, South Carolina, United States

U

Ulrika Birgersdotter-Green

US San Diego Health, San Deigo, California, United States

L

Lars Eckardt

University of Munster, Munster, Germany

B

Bradley Knight

Northwestern University, Chicago, Illinois, United States

R

Reinoud Knops

Amsterdam University Medical Center, Amsterdam, Netherlands

C

Christelle Marquie

Department of Cardiology, University Hospital of Lille, Lille, France (C.M.).

S

Stefano Viani

University Hospital of Pisa, Pisa, Italy

L

Lucas Boersma

St.Antonius Hospital, Nieuwegein, Netherlands

A

Amy Brisben

Boston Scientific, St. Paul, Minnesota, United States

M

Madelyn Duffy

Boston Scientific, St. Paul, Minnesota, United States

M

Mikhael El-Chami

Emory University School of Medicine, Atlanta, Georgia, United States

A

Andrea Russo