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Arrhythmic manifestations in patients with congenital left ventricular aneurysms and diverticula
Laurent M Haegeli1, Ercüment Ercin, Thomas Wolber
1Clinic for Cardiology, Cardiovascular Center, University of Zurich, Switzerland. laurent.haegeli@usz.ch
Insights
Congenital left ventricular aneurysms and diverticula (LVA/Ds) can cause ventricular arrhythmias, often presenting as ventricular tachycardia (VT). Electrophysiology testing frequently reproduces these arrhythmias in affected patients.
Area of Science:
- Cardiology
- Cardiac Electrophysiology
- Congenital Heart Disease
Background:
- Congenital left ventricular aneurysms and diverticula (LVA/Ds) are rare cardiac malformations.
- Arrhythmic manifestations, including ventricular arrhythmias, can occur in patients with LVA/Ds.
Purpose of the Study:
- To investigate the clinical characteristics of patients with congenital LVA/D presenting with arrhythmic manifestations.
- To determine the prevalence and type of arrhythmias in this patient cohort.
Main Methods:
- Retrospective analysis of 250 patients diagnosed with congenital LVA/D over 20 years.
- Diagnosis confirmed by echocardiography after excluding other cardiac conditions.
- Evaluation of arrhythmic manifestations, including electrocardiographic recordings and electrophysiologic testing.
Main Results:
- 13% of patients (32/250) presented with arrhythmias, predominantly ventricular tachycardia (VT).
- Common symptoms included syncope, presyncope, and palpitations.
- Electrophysiologic testing induced VT in 9 out of 12 tested patients, often mimicking spontaneous arrhythmias.
Conclusions:
- Patients with congenital LVA/Ds presenting with arrhythmias frequently exhibit VT.
- Electrophysiologic testing is valuable for reproducing clinical VT in these patients.
- Congenital LVA/D should be considered in the differential diagnosis of ventricular arrhythmias.
Abstract:
Congenital left ventricular aneurysms and diverticula (LVA/Ds) are rare cardiac malformations that can be detected using echocardiography or other imaging techniques. Some of these patients present with ventricular arrhythmias. This study investigated clinical characteristics of patients with congenital LVA/D presenting with arrhythmic manifestations. Over the previous 20 years 250 patients were diagnosed to have congenital LVA/D at our institution. Diagnosis was made using echocardiography after exclusion of coronary artery disease, local cardiac inflammatory processes, traumatic causes, or cardiomyopathies. At initial presentation 32 of the 250 patients (13%, average age 45 years, range 25 to 65, 21 men and 11 women) exhibited arrhythmias. At least 2 LVA/Ds were present in 6 of these patients. LVA/Ds were localized at the posterobasal, apical, anteroseptal, and anterolateral walls in 12, 11, 4, and 5 patients, respectively. The most common complaints at presentation were syncope or presyncope in 18 patients and palpitations in 11 patients. One patient had survived sudden cardiac death. Long-term electrocardiographic recordings showed ventricular tachycardia (VT) or ventricular fibrillation in 17 patients (53%). Twelve patients underwent electrophysiologic testing. Nine patients had inducible ventricular tachyarrhythmia, whereas induced tachycardia was similar to that during spontaneous arrhythmia in 7 patients. In conclusion, patients with congenital LVA/Ds who present with arrhythmic manifestations commonly have VT. Electrophysiologic testing can reproduce clinical VT in most of these patients.
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