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Updated: Jun 20, 2026

Programmed Electrical Stimulation in Mice
Published on: May 26, 2010
Programmed ventricular stimulation for risk stratification in patients with myocardial scarring and mildly reduced or
Auriane Soris1, Claudia Herrera-Siklody1, Adrian Luca1
1Arrhythmia Unit, Cardiovascular Department, Centre Hospitalier Universitaire Vaudois and University of Lausanne, Lausanne, Switzerland.
Background:
Implantable cardioverter defibrillators (ICDs) are recommended in patients with left ventricular ejection fraction (LVEF) of ≤35%. However, no recommendation exists to guide the use of prophylactic ICD in patients with less altered LVEF and myocardial scarring, even though they represent most of sudden cardiac deaths.
Objective:
This study aimed to evaluate the prognostic value of programmed ventricular stimulation (PVS) in patients with mildly reduced or preserved LVEF.
Methods:
Patients who underwent PVS with myocardial scarring and LVEF of ≥40% were included. The primary endpoint was the occurrence of a major arrhythmic event (MAE), namely sudden cardiac death, ventricular tachycardia/fibrillation, and appropriate ICD therapy.
Results:
A total of 168 patients were included (mean age, 62 ± 13 years; LVEF, 54% ± 9%). Indication for PVS was mostly nonsustained ventricular tachycardia and/or syncope (83%). Patients with post-myocardial infarction represented approximately half of the cases (52%). Inducibility during PVS was observed in 21 patients (13%). Over a mean follow-up of 46 ± 38 months, an MAE occurred in 9 patients with positive PVS (43%) vs 4 patients (2.7%) with negative PVS. Inducibility during PVS provided high rule-out performance with a 97% negative predictive value for the prediction of MAE and a fair rule-in performance with a 43% positive predictive value (sensitivity 69%; specificity 92%).
Conclusion:
PVS is a useful tool to discriminate patients with myocardial scar and LVEF of ≥40% at an increased arrhythmic risk. Effective utilization of ICD may be anticipated in the case of positive PVS, whereas noninducible patients are at a lower MAE risk.
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