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Aortopexy in severe tracheal instability: short-term and long-term outcome in 29 infants and children
J F Vazquez-Jimenez1, J S Sachweh, O J Liakopoulos
1Department of Thoracic and Cardiovascular Surgery, University Hospital RWTH Aachen, Germany. jvazquez-jimenez@post.klinikum.rwth-aachen.de
Insights
Aortopexy effectively treats life-threatening apneas caused by tracheal instability after esophageal atresia surgery. While safe with no mortality, it does not prevent increased respiratory infections long-term.
Area of Science:
- Pediatric Surgery
- Thoracic Surgery
- Critical Care Medicine
Background:
- Tracheal instability is a significant risk following esophageal atresia repair.
- Life-threatening apneas can occur due to flaccid trachea or external vascular compression.
- Aortopexy is a surgical intervention considered for these severe cases.
Purpose of the Study:
- To retrospectively analyze the efficacy and outcomes of aortopexy.
- To evaluate both short-term and long-term results of the procedure.
- To assess the safety profile of aortopexy in pediatric patients.
Main Methods:
- A retrospective review of 29 patients operated on between 1985 and 2000.
- Patients presented with life-threatening apneas secondary to tracheal instability or vascular compression.
- The surgical technique involved ventropexy of the aortic arch to the sternum and ventral thoracic wall.
Main Results:
- No early or late mortality was observed in the study cohort.
- A significant improvement or resolution of apneic symptoms occurred within days to 3 months post-surgery.
- Complications included reversible phrenic nerve lesions (2), pneumothorax (3), and wound healing issues (1).
Conclusions:
- Aortopexy is a safe procedure with no associated mortality and low morbidity.
- The surgery is highly effective in preventing recurrent life-threatening apneas.
- Long-term follow-up indicated an increased susceptibility to respiratory infections despite successful apnea management.
Background:
Tracheal instability is a hazardous situation after operation for esophageal atresia. In cases with life-threatening apneas, aortopexy is a therapeutic option. To assess efficacy, short-term and long-term outcome was analyzed retrospectively.
Methods:
Between 1985 and 2000, 29 patients (age, 1.5 months to 5.2 years) were operated on. A flaccid trachea after operation for esophageal atresia was the cause for life-threatening apneas in 27, and there was external vascular compression in 2 patients. The operative procedure consisted of ventropexy of the aortic arch to the sternum and ventral thoracic wall.
Results:
There was neither early nor late mortality. A reversible lesion of the phrenic nerve was observed in 2 patients, a pneumothorax in 3, and secondary wound healing in 1. In all but 1 patient symptoms improved markedly or disappeared within days or within the first 3 months postoperatively. An increased susceptibility to respiratory infections was observed in long-term follow-up.
Conclusions:
Aortopexy can be performed with no mortality and low morbidity. Aortopexy is effective to prevent further life-threatening apneas, but does not prevent an increased susceptibility to respiratory infections.
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