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Updated: Apr 9, 2026

Echocardiographic Evaluation of Atrial Communications before Transcatheter Closure
Published on: February 8, 2022
Diagnosis and management of aorto-left ventricular tunnel
Pallavi Kathare1, Rama G Subramanyam2, Tapan Kumar Dash3
1Department of Cardiac Surgery, Gutti, Consultant Pediatric Cardiologist, Care Hospital, Hyderabad, Telangana, India.
Insights
Aorto-left ventricular tunnel (ALVT) is a rare congenital heart defect requiring prompt surgical correction. Surgical intervention offers the best outcomes for this potentially fatal anomaly, while catheter closure has limited efficacy.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Pediatric Cardiology
Background:
- Aorto-left ventricular tunnel (ALVT) is a rare congenital extracardiac channel.
- ALVT can lead to progressive left ventricular dilatation and heart failure.
- Early correction is crucial for managing ALVT.
Purpose of the Study:
- To report the diagnosis and management of aorto-left ventricular tunnel (ALVT).
- To evaluate treatment outcomes for ALVT over an 11-year period.
- To compare surgical and transcatheter closure methods for ALVT.
Main Methods:
- Retrospective analysis of seven patients with ALVT.
- Diagnosis confirmed by transthoracic echocardiogram.
- Evaluation of surgical and transcatheter closure techniques.
Main Results:
- Two patients refused treatment and died.
- Four patients underwent surgical closure; one required a Bentall procedure.
- Transcatheter closure had limited success, with one case requiring surgical revision due to hemolysis.
Conclusions:
- Aorto-left ventricular tunnel (ALVT) is a rare, potentially fatal anomaly.
- Surgical management is the preferred treatment for ALVT.
- Transcatheter closure has a limited role in ALVT management.
Background:
Aorto-left ventricular tunnel (ALVT) is a rare congenital extracardiac channel with progressive left ventricular dilatation needs early correction.
Materials And Methods:
This is a report of diagnosis and management of aorto-left ventricular tunnel (ALVT) over a period of 11 years from a single institution. Seven patients (age range: 7 days-45 years) presented with heart failure. The diagnosis of ALVT was made by transthoracic echocardiogram in all cases.
Results:
Treatment was refused by two patients who died during follow-up. Surgical closure of the tunnel was done in four cases, of which one needed Bentall procedure. Two patients had residual leak after the surgery. Transcatheter closure using Amplatzer muscular device was performed in two cases (for postoperative residual leak in one and primary procedure in the other). Significant hemolysis developed in one of them, necessitating the removal of the device and closed surgically. This child underwent aortic valve replacement two years later. All the remaining patients were doing well during the median follow-up of 30 months (range: 1.5-9 years).
Conclusion:
ALVT is a rare and potentially fatal anomaly that is ideally managed surgically. Catheter closure has a limited role.
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