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Postpneumonectomy syndrome in children: advantages and long-term follow-up of expandable prosthesis
G Podevin1, M Larroquet, C Camby
1CHU Hotel Dieu, Nantes, and the Hôpital A. Trousseau, Paris, France.
Insights
Intrathoracic prostheses effectively treat post-pneumonectomy syndrome in children, improving respiratory function and allowing for growth. This surgical intervention corrects severe mediastinal shift and bronchial stretching, enhancing patient outcomes.
Area of Science:
- Pediatric Thoracic Surgery
- Respiratory Medicine
- Biomedical Engineering
Background:
- Pneumonectomy in children can cause severe mediastinal shift, leading to bronchial stretching and respiratory failure.
- Post-pneumonectomy syndrome presents a significant challenge in pediatric surgical care.
Purpose of the Study:
- To evaluate the efficacy of intrathoracic prosthesis insertion for correcting post-pneumonectomy syndrome in children.
- To assess the impact of expandable prostheses on mediastinal position and respiratory function.
Main Methods:
- Retrospective analysis of 42 children undergoing pneumonectomy, with 7 treated for post-pneumonectomy syndrome.
- Surgical insertion of expandable prostheses, with periodic saline injections to maintain mediastinal position.
- Follow-up included pulmonary function tests and assessment of prosthesis management, including replacement with breast prostheses in adolescence.
Main Results:
- A mean of 5 years post-pneumonectomy before prosthesis implantation.
- Significant improvement in obstructive syndrome observed in most patients post-intervention.
- Mean follow-up of 6 years with all patients demonstrating positive outcomes.
Conclusions:
- Intrathoracic prosthesis insertion dramatically improves clinical symptoms and reduces obstructive syndrome.
- Expandable prostheses facilitate progressive, well-tolerated mediastinal repositioning and accommodate growth.
- This approach offers a viable solution for managing post-pneumonectomy syndrome in pediatric patients.
Background/Purpose:
Pneumonectomy in children can be complicated by a severe mediastinal shift, which leads to bronchial stretching resulting in severe respiratory failure. This postpneumonectomy syndrome can be corrected by inserting a prosthesis in the empty side of the chest.
Methods:
Forty-two children, from 6 months to 15 years old, underwent a pneumonectomy. Seven of these patients were treated surgically for severe manifestations of postpneumonectomy syndrome. First insertion of an expandable prosthesis was followed up in 5 cases by its replacement with a breast prosthesis in adolescence. The expandable prosthesis was injected periodically with saline solution to maintain the mediastinum in a midline position as the children grew.
Results:
The mean delay between pneumonectomy and first prosthesis implantation was 5 years (range, 11 months to 8 years). Pulmonary function tests showed a substantial improvement in the obstructive syndrome in all patients except one, in whom the functional improvement was moderate. The mean follow-up after the expandable prosthesis implantation was 6 years (range, 6 months to 10 years) and all patients are doing well.
Conclusions:
The insertion of an intrathoracic prosthesis can dramatically improve the clinical symptoms and reduce the functional obstructive syndrome. The expandable prosthesis allowed for progressive, well-tolerated recentering of the mediastinum and adjustment for growth.
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