Surgical management of aortopulmonary window with pulmonary artery dilatation causing left main coronary compression
Anand Kumar Mishra1, Sanjeev Hanumantacharya Naganur2, Vidur Bansal1
1Department of Cardiothoracic and Vascular Surgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Insights
A rare congenital heart defect, aortopulmonary window, can cause serious complications. Surgical closure successfully treated a 14-year-old boy experiencing cardiac issues during device closure for this condition.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Pediatric Cardiology
Background:
- Aortopulmonary window is a rare congenital heart defect.
- Enlarged pulmonary artery can cause extrinsic compression of the left main coronary artery, leading to chest pain and sudden cardiac death, especially in pulmonary hypertension.
- This case highlights a rare complication in a pediatric patient.
Observation:
- A 14-year-old boy with a large aortopulmonary window was scheduled for device closure.
- During the procedure, ST-T segment changes occurred, indicating potential myocardial ischemia.
- The device closure was abandoned due to procedural complications.
Findings:
- The patient experienced acute cardiac changes during attempted device closure of the aortopulmonary window.
- These changes suggested significant hemodynamic compromise or direct coronary compromise.
- Surgical intervention was required for definitive treatment.
Implications:
- Device closure may pose risks in cases with significant pulmonary artery enlargement or complex anatomy.
- Surgical closure remains a safe and effective alternative for aortopulmonary window, especially when device closure is contraindicated or complicated.
- Early recognition and management of intra-procedural complications are crucial in pediatric cardiac interventions.
Abstract:
Aortopulmonary window is a rare congenital heart defect. Left main coronary artery extrinsic compression by an enlarged pulmonary artery is a rare complication and a potential cause for chest pain and sudden cardiac death in patients with pulmonary hypertension. Here, we present the case of a 14-year-old boy with a large aortopulmonary window who was planned for a device closure, but during the procedure, he developed ST-T segment changes while the device was being deployed, and hence the procedure was abandoned. The boy subsequently underwent a successful surgical closure thereafter.
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