Key result
Arrhythmic MVP and mitral annular disjunction heighten sudden cardiac death risk, requiring tailored stratification.
Why the study?
The mechanisms underlying serious cardiac arrhythmias in patients with mitral valve prolapse and mitral annular disjunction are not fully understood, and tailored risk stratification is crucial due to increased sudden cardiac death risk.
This review highlights the pathophysiology, diagnostic deviations, and risk stratification for sudden cardiac death in patients with arrhythmic mitral valve prolapse and mitral annular disjunction.
Mitral valve prolapse (MVP) and mitral annular disjunction (MAD) are common comorbidities that can lead to serious cardiac arrhythmias and sudden cardiac death (SCD). Arrhythmic MVP is characterized by the presence of MVP with frequent (over 5% ventricular extra beats) and/or complex ventricular arrhythmias, such as ventricular tachycardia (VT), non-sustained VT, or ventricular fibrillation in the absence of other causes of arrhythmia, e.g., post-infarction scar, recent ischemia, channelopathy, or cardiomyopathy. The mechanisms of the development of serious cardiac arrhythmias in patients with MVP and MAD are not fully understood. Arrhythmic MVP may be an indication for cardioverter defibrillator implantation. Considering the increased risk of SCD in this group of patients, the pathophysiology of this valvular dysfunction and characteristic deviations in diagnostic tests that indicate a higher risk of SCD are presented. The issue of tailored risk stratification in individual patients is crucial.
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Dworak et al. (2026) conducted a review in Arrhythmic Mitral Valve Prolapse and Mitral Annular Disjunction. Arrhythmic mitral valve prolapse and mitral annular disjunction increase the risk of serious cardiac arrhythmias and sudden cardiac death, necessitating tailored risk stratification.
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