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Effective Management of Peritoneal Dialysis-Associated Hydrothorax in a Child: A Case Report
Cahyani Gita Ambarsari1, Evita Karianni Bermanshah1, Muhammad Arza Putra2
1Department of Child Health, Faculty of Medicine, Universitas Indonesia, Cipto Mangunkusumo Hospital, Jakarta Pusat, Indonesia.
Insights
A rare complication of peritoneal dialysis (PD) in children, pleuroperitoneal leaks causing hydrothorax, can be managed. Temporary hemodialysis (HD) and pleurodesis effectively resolved hydrothorax in a pediatric case.
Area of Science:
- Pediatric Nephrology
- Thoracic Surgery
- Medical Imaging
Background:
- Peritoneal dialysis (PD) offers quality of life benefits for pediatric end-stage renal disease patients.
- Pleuroperitoneal leaks, leading to hydrothorax, are known PD complications.
Observation:
- A 9-year-old boy on continuous ambulatory PD (CAPD) developed hydrothorax and pneumonia.
- Imaging confirmed a pleuroperitoneal fistula (PPF) with significant dialysate leakage.
- Surgical repair was complicated by pleural adhesions due to pneumonia.
Findings:
- The patient was temporarily switched to hemodialysis (HD).
- Pleurodesis with bleomycin successfully treated the right pleural effusion.
- PD was reinitiated without recurrence of hydrothorax after 10 weeks of HD.
Implications:
- This case highlights PPF as a cause of hydrothorax in pediatric PD patients.
- A strategy of temporary HD and pleurodesis can effectively manage this complication.
- Early recognition and management are crucial for successful PD continuation.
Abstract:
Peritoneal dialysis (PD) confers many advantages, including a better quality of life for children with end-stage renal disease; however, the procedure is associated with several complications, including pleuroperitoneal leaks. Here, we report an unusual case of hydrothorax caused by long-term PD in a child, which was further complicated by pneumonia. A 9-year-old boy who had received CAPD for 22 months presented with dyspnea, swelling, and increased body weight. Chest tube drainage yielded 500 mL of transudative fluid. Computed tomography peritoneography revealed increased outflow from the peritoneum to the pleural cavity. PD was suspended, and hemodialysis (HD) was initiated. Video-assisted thoracoscopic surgery was performed; however, because the patient had pneumonia during hospitalization, pleural adhesions with a septated appearance occurred. This resulted in difficulties identifying pleuroperitoneal fistula (PPF). Right pleural effusion resolved following pleurodesis using bleomycin. Regular HD was performed for 10 weeks, and PD was subsequently reinitiated. There was no recurrence of hydrothorax during long-term follow-up. We suspect that the underlying mechanism of hydrothorax in our patient was associated with a PPF that formed either due to a congenital diaphragmatic defect or an acquired defect, resulting in dialysate leakage. Our case demonstrates that a temporary switch from PD to HD, accompanied by pleurodesis, may help resolve hydrothorax that occurs as a complication of long-term PD.
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