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The impact of chylothorax on neonates with repaired congenital diaphragmatic hernia
Shauna M Levy1, Pamela A Lally, Kevin P Lally
1Center for Surgical Trials and Evidence-based Practice, Departments of Pediatric Surgery and Surgery, The University of Texas Medical School At Houston, Houston, TX 77030, USA.
Insights
Chylothorax is a rare complication after congenital diaphragmatic hernia (CDH) repair in neonates. Key risk factors include patch repair and extracorporeal membrane oxygenation (ECMO), but survival is not significantly impacted.
Area of Science:
- Neonatal surgery
- Pediatric thoracic surgery
- Critical care medicine
Background:
- Chylothorax is a recognized complication following surgical repair of congenital diaphragmatic hernia (CDH) in newborns.
- Understanding risk factors and outcomes is crucial for managing this condition.
Purpose of the Study:
- To evaluate risk factors, treatment strategies, morbidity, and survival rates associated with chylothorax in neonates after CDH repair.
- Utilize a large international registry for a comprehensive analysis.
Main Methods:
- Prospective evaluation of neonates with repaired, unilateral CDHs from January 2007 to January 2010.
- Diagnosis of chylothorax based on pleural fluid examination.
- Analysis of patient characteristics, CDH severity, treatment, and survival, including the role of extracorporeal membrane oxygenation (ECMO).
Main Results:
- Chylothorax occurred in 4.6% of 1383 neonates.
- Patch repair and ECMO were significant risk factors; repair on or after ECMO increased odds of chylothorax.
- Conservative treatment was successful in 83.1% of cases.
- Chylothorax was associated with increased oxygen use and longer hospital stays but not decreased survival.
Conclusions:
- Chylothorax is an uncommon but significant complication of neonatal CDH repair.
- Increased disease severity, particularly repair on or after ECMO, elevates chylothorax risk.
- Conservative management is often effective, leading to morbidity but not mortality.
Purpose:
Chylothorax is a known complication in neonates after congenital diaphragmatic hernia (CDH) repair. This report uses a large international registry to evaluate risk factors, treatment, morbidity, and survival associated with chylothorax in a prospective cohort of neonates after CDH repair.
Methods:
From January 2007 to January 2010, live-born neonates with repaired, unilateral CDHs were evaluated from a prospective database for chylothorax development. Chylothorax was diagnosed based on pleural fluid examination. Study variables included patient characteristics, CDH defect and disease severity characteristics, chylothorax treatment, and survival. In addition, the temporal relationship between timing of CDH repair and extracorporeal membrane oxygenation (ECMO) therapy was evaluated as a risk factor for chylothorax. Univariate and multivariate regression analyses were utilized.
Results:
Among the 1383 patients evaluated, chylothorax was diagnosed in 4.6% of the cohort. Patch repair and ECMO were statistically significant risk factors for chylothorax. The odds of developing a chylothorax were significantly increased in patients with CDH repair on ECMO (aOR 2.6; 95% CI: 1.3-4.9) or after ECMO (aOR 3.1; 95% CI: 1.7-5.8). Most chylothoraces (83.1%) were successfully treated without surgery. Chylothorax patients had significant morbidity including increased oxygen use at 30days and longer length of stay. Survival was not significantly affected by chylothorax.
Conclusions:
Chylothorax is a known but uncommon complication of neonatal CDH repair. In this very large series of chylothorax in association with CDH, major risk factors appear to be related to increased disease severity with the highest risk in patients repaired on or after ECMO. Chylothoraces usually improve with conservative therapy and lead to significant morbidity but not increased mortality.
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