Key result
Inducible ventricular arrhythmias during programmed stimulation predict ~690% greater clinical arrhythmia risk in arrhythmic MVP.
Why the study?
Arrhythmic mitral valve prolapse carries an increased risk of sudden cardiac death, but current risk stratification relies mainly on clinical and imaging markers while the role of programmed ventricular stimulation remains uncertain.
Does programmed ventricular stimulation predict clinically significant ventricular arrhythmias in patients with arrhythmic mitral valve prolapse syndrome?
Cohort (n=42)
No
Does programmed ventricular stimulation predict clinically significant ventricular arrhythmias in patients with arrhythmic mitral valve prolapse syndrome?
Odds Ratio: 7.9 (95% CI 1.31–47.51)
Absolute Event Rate: 45% vs 9.1%
p-value: p=0.024
Inducible ventricular arrhythmias during programmed ventricular stimulation are associated with a significantly higher risk of subsequent clinically significant ventricular arrhythmias in patients with arrhythmic mitral valve prolapse syndrome.
Inducible VA on PVS was associated with higher clinical event rates in AMVP; supports prospective evaluation of PVS for risk stratification but should not yet change practice.
Background Mitral valve prolapse (MVP) is commonly benign, but an arrhythmic phenotype (AMVP) with increased risk for sudden cardiac death has been described. Current risk stratification is mainly based on clinical data and imaging markers, while the role of programmed ventricular stimulation (PVS) remains uncertain. Methods In this prospective single-center cohort study, 42 patients fulfilling the EHRA consensus criteria for AMVP underwent an electrophysiological study with programmed ventricular stimulation between 2016 and 2025. Stimulation was performed from the right ventricular apex and outflow tract using up to two extra stimuli. Following shared decision-making, patients received either an implantable cardioverter-defibrillator (ICD) or an implantable loop recorder (ILR). The endpoint was the occurrence of clinically significant ventricular arrhythmias (VAs), defined as appropriate ICD therapies, ILR-documented sustained VT, or arrhythmic syncope. Results Sustained ventricular arrhythmias were inducible in 20 patients (47.6%). ICD implantation was performed in 14 patients (70%) with inducible VA and in 6 patients (27.3%) without VA inducibility. During a mean follow-up of 38.0 ± 24.6 months, clinically significant VA occurred in 45.0% of patients with inducible VA vs. 9.1% of patients with nonpathological PVS ( p = 0.01). Conclusion Inducible ventricular arrhythmias during PVS were associated with subsequent clinically significant VA in AMVP. PVS may serve as an additional risk stratification tool in this entity.
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Rath et al. (2026) conducted a cohort in Arrhythmic mitral valve prolapse syndrome (n=42). Inducible ventricular arrhythmias during programmed ventricular stimulation vs. Non-inducible ventricular arrhythmias was evaluated on Clinically significant ventricular arrhythmias (appropriate ICD therapies, ILR-documented sustained VT, or arrhythmic syncope) (OR 7.90, 95% CI 1.31-47.51, p=0.024). Inducible ventricular arrhythmias during programmed ventricular stimulation predicted clinically significant arrhythmias in arrhythmic mitral valve prolapse (45.0% vs 9.1%, OR 7.90).
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