Surgical Management of Aortopulmonary Window and its Associated Cardiac Lesions
Chinnaswamy Reddy1, Ameya Kaskar1, Eswara Karthick1
1Department of Cardiothoracic Surgery, 501944Narayana Institute of Cardiac Sciences, Narayana Health, Bangalore, Karnataka, India.
Insights
Surgical repair of aortopulmonary window shows excellent outcomes when it is an isolated defect. Outcomes are less favorable but still good for patients with associated cardiac anomalies, with pulmonary artery hypertensive crisis being a key predictor of early mortality.
Area of Science:
- Cardiology
- Pediatric Cardiac Surgery
- Congenital Heart Disease
Background:
- Aortopulmonary window is a rare congenital heart defect.
- Surgical repair is the standard treatment.
- Outcomes can vary based on the presence of associated cardiac anomalies.
Purpose of the Study:
- To review institutional experience with surgical repair of aortopulmonary window.
- To compare outcomes between isolated aortopulmonary window and those with associated lesions.
- To identify predictors of early mortality and long-term outcomes.
Main Methods:
- Retrospective review of 183 patients undergoing surgical repair of aortopulmonary window from 2006-2020.
- Patients were divided into two groups: isolated aortopulmonary window (n=120) and associated lesions (n=63).
- Analysis of early mortality, long-term survival, and freedom from reintervention.
Main Results:
- Early mortality was significantly higher in patients with associated lesions (12.7%) compared to isolated aortopulmonary window (0.8%).
- Pulmonary artery hypertensive crisis was the only independent predictor of early mortality on multivariable analysis.
- Five- and 8-year survival rates were 77% ± 6.5% for associated lesions and 98.8% ± 1.2% for isolated lesions.
Conclusions:
- Surgical repair of isolated aortopulmonary window yields excellent early and long-term outcomes.
- Patients with associated lesions have higher early mortality, but still achieve good long-term survival and freedom from reoperation.
- Pulmonary artery hypertensive crisis is a critical factor influencing early mortality in this patient population.
Abstract:
Background: The aim of this study was to review our institutional experience with patients who underwent surgical repair of aortopulmonary window, either as an isolated lesion or in association with other cardiac anomalies. Methods: Between January 2006 and December 2020, 183 patients underwent surgical repair of aortopulmonary window at our institute. Sixty-three patients had associated lesions (Group 1); 120 patients had isolated aortopulmonary window (Group 2). Median age was 7 months. Results: The early mortality in Group 1 was significantly higher (12.7%) compared to Group 2 (0.8%) (P = .001). The most common associated anomaly was ventricular septal defect (29 patients). On univariable analysis, cardiopulmonary bypass time (P < .001), aortic cross-clamp time (P < .001), delayed chest closure (P = .02), sepsis (P = .006), tracheostomy (P = .002), extracorporeal membrane oxygenation (P < .001), associated lesions (P = .001), pulmonary artery hypertensive crisis (P < .001) were predictors for early mortality. On multivariable analysis only pulmonary artery hypertensive crisis was identified as predictor for early mortality (P = .03; odds ratio = 24). Survival at both 5 years and 8 years was 77% ± 6.5 in Group 1 and 98.8% ± 1.2 in Group 2 (P≤.001). Freedom from reintervention at both 5 years and 8 years was 92.4% ± 5.2 in Group 1 and 100% in Group 2 (P = .055). Conclusion: Early outcomes of aortopulmonary window repair are excellent among patients in which this is an isolated lesion, as compared to those with associated lesions. Long-term outcomes in terms of freedom from reoperation are excellent in both the groups.
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