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Hemodynamic Precision in the Neonatal Intensive Care Unit using Targeted Neonatal Echocardiography
Published on: January 27, 2023
A natural systemic to pulmonary artery shunt
Santhosh Regini Benjamin1, Roy Thankachen1, Deepak Narayanan1
1The Department of Cardiothoracic Surgery, The Christian Medical College, CMC Hospital, Vellore, 632004 Tamil Nadu India.
A rare left subclavian artery anomaly associated with a right aortic arch effectively served as a natural shunt for tetralogy of Fallot (TOF). Surgical correction of TOF and ligation of this aberrant artery were successfully performed.
Area of Science:
- Cardiovascular Surgery
- Pediatric Cardiology
- Congenital Heart Disease
Background:
- Isolation of the left subclavian artery is a rare anomaly, often linked with a right aortic arch.
- Tetralogy of Fallot (TOF) is a complex congenital heart defect requiring surgical intervention.
- Aberrant subclavian arteries can have significant clinical implications.
Purpose of the Study:
- To report a unique case of an isolated left subclavian artery supplying pulmonary circulation in a patient with TOF.
- To describe the successful surgical management of this complex anatomical variation.
- To highlight the role of this anomaly as a natural systemic-to-pulmonary shunt.
Main Methods:
- Case report detailing a patient with TOF and an aberrant left subclavian artery.
- Pre-operative assessment including evaluation for associated symptoms.
- Surgical intervention involving total correction of TOF and ligation of the aberrant artery.
Main Results:
- The aberrant left subclavian artery provided a functional systemic-to-pulmonary artery shunt, maintaining adequate oxygenation.
- The patient exhibited good room air saturation without signs of vertebrobasilar insufficiency or limb ischemia.
- Successful total correction of TOF and ligation of the aberrant artery were achieved.
Conclusions:
- An isolated left subclavian artery can act as a natural palliative shunt in TOF.
- Surgical correction of TOF is feasible and effective even with this rare anomaly.
- Careful pre-operative assessment is crucial for managing such complex congenital heart conditions.
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