Abstract
Congenital cardiac patients who received neonatal reconstructive aortic arch surgery are at risk of aortopulmonary space narrowing with compression of the left pulmonary artery and left main bronchus (LMB) later in life. We discuss a challenging adolescent single ventricle patient who presented for surgical treatment of a non-idiopathic thoracic scoliosis (posterior spinal fusion) with severe stenosis of the LMB and left pulmonary artery due to a narrow aortopulmonary space. Careful preoperative imaging, evaluation, and decision making resulted in successful surgical treatment and uneventful perioperative course.
| Original language | English |
|---|---|
| Pages (from-to) | 221-225 |
| Number of pages | 5 |
| Journal | Seminars in Cardiothoracic and Vascular Anesthesia |
| Volume | 26 |
| Issue number | 3 |
| Early online date | 11 Aug 2022 |
| DOIs | |
| Publication status | Published - Sept 2022 |
Keywords
- ACHD
- adult congenital heart disease
- airway Malacia
- aortapulmonary space
- cardiac anesthesia
- congenital heart disease
- Fontan
- GUCH
- non-cardiac surgery
- single ventricle
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