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A Pulmonary Trunk Banding Model of Pressure Overload Induced Right Ventricular Hypertrophy and Failure
Published on: November 29, 2018
Surgical management of aortopulmonary window
1Department of Cardiovascular Surgery, Kyushu Kosei-Nenkin Hospital, Kitakyushu, Japan.
Surgical repair of aortopulmonary window (APW) in children, even with complex heart defects like interrupted aortic arch, yields encouraging results. Most patients experience a good long-term outcome after APW repair.
Area of Science:
- Pediatric Cardiology
- Congenital Heart Surgery
- Vascular Malformations
Background:
- Aortopulmonary window (APW) is a rare congenital heart defect characterized by abnormal communication between the aorta and pulmonary artery.
- APW often presents with other complex cardiac anomalies, posing surgical challenges.
Purpose of the Study:
- To present surgical experience with aortopulmonary window repair in pediatric patients.
- To evaluate the long-term outcomes of surgical intervention for APW, particularly in the presence of associated anomalies.
Main Methods:
- Retrospective analysis of 13 children undergoing surgical repair of aortopulmonary window.
- Patients' ages ranged from 3 days to 1 year, with various associated congenital heart lesions including interrupted aortic arch.
- Surgical repair involved cardiopulmonary bypass in 11 patients and ligation in 2.
Main Results:
- A single mortality (7.7%) occurred in a patient with tricuspid atresia.
- No late deaths were observed during a mean follow-up of 7 years and 3 months.
- The majority of patients demonstrated favorable long-term outcomes.
Conclusions:
- Surgical repair of aortopulmonary window is effective and yields encouraging results, even in complex cases with major cardiac anomalies.
- Patients with aortopulmonary window, including those with interrupted aortic arch, can achieve good long-term outcomes following surgical correction.
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