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Lung Volume Reduction Surgery for Respiratory Failure in Infants With Bronchopulmonary Dysplasia
Bongyeon Sohn1, Samina Park1, In Kyu Park1
1Department of Thoracic and Cardiovascular Surgery, Seoul National University Hospital, Seoul, South Korea.
Insights
Lung volume reduction surgery (LVRS) offers a new treatment option for pediatric patients with severe emphysematous lung disease. This surgical intervention shows promise in improving respiratory function and weaning patients from mechanical ventilation.
Area of Science:
- Pediatric surgery
- Pulmonology
- Critical care medicine
Background:
- Lung volume reduction surgery (LVRS) is established for severe emphysema in adults.
- LVRS has not been previously reported in pediatric populations.
- Pediatric patients with severe lung disease often require prolonged mechanical ventilation.
Observation:
- Two preterm infant girls with severe bronchopulmonary dysplasia and respiratory failure underwent LVRS.
- Case 1: Postnatal ventilation, pulmonary hypertension, hypothyroidism. LVRS performed via sternotomy.
- Case 2: Postnatal ventilation, pulmonary hypertension, multiple congenital anomalies. LVRS performed via thoracotomy.
Findings:
- Case 1: Improved respiratory function, discontinued ventilator and oxygen support, T-cannula removed.
- Case 2: Successfully weaned from mechanical ventilator within 1 month, discharged without major complications, now on intermittent home ventilation.
- Both cases demonstrate positive outcomes following pediatric LVRS.
Implications:
- LVRS can be a viable treatment option for pediatric patients with severe emphysematous lung conditions.
- This surgical approach may facilitate discontinuation of prolonged mechanical ventilator care in pediatric respiratory failure.
- Further research into pediatric LVRS is warranted to establish its efficacy and safety profile.
Abstract:
Lung volume reduction surgery (LVRS) can be performed in patients with severe emphysematous disease. However, LVRS in pediatric patients has not yet been reported. Here, we report our experience with 2 cases of pediatric LVRS. The first patient was a preterm infant girl with severe bronchopulmonary dysplasia, pulmonary hypertension, and hypothyroidism. The emphysematous portion of the right lung was removed via sternotomy and right hemiclamshell incision. The patient was discharged on full-time home ventilator support for 3 months after the surgery. Since then, her respiratory function has improved continuously. She no longer needs oxygen supplementation or ventilator care. Her T-cannula was removed recently. The second patient was also a preterm infant girl with bronchopulmonary dysplasia. She was born with pulmonary hypertension and multiple congenital anomalies, including an atrial septal defect. Despite receiving the best supportive care, she could not be taken off the mechanical ventilator because of severe hypercapnia. We performed LVRS on the right lung via thoracotomy. She was successfully weaned off the mechanical ventilator 1 month after the surgery. She was discharged without severe complications at 3 months after the operation. At present, she is growing well with the help of intermittent home ventilator support. She can now tolerate an oral diet. Our experience shows that LVRS can be considered as a treatment option for pediatric patients with severe emphysematous lung. It is especially helpful for discontinuing prolonged mechanical ventilator care for patients with respiratory failure.
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