Congenital Diaphragmatic Hernia: Causes, Prenatal Management, and Surgical Options
A subchorionic hemorrhage does not cause congenital diaphragmatic hernia (CDH), as CDH develops during early embryonic development around the 8th week of gestation due to incomplete formation of the diaphragm. 1 The diaphragmatic hernia diagnosed at 20 weeks was likely already present before the subchorionic hemorrhage was identified at 15 weeks.
Etiology of Congenital Diaphragmatic Hernia
CDH is a developmental defect that occurs during early embryonic formation:
- Develops during the 8th week of gestation when the diaphragm fails to form completely 1
- Most commonly presents as a Bochdalek hernia (95% of cases), typically on the left side (80-85%) 1, 2
- Results in abdominal organs entering the thoracic cavity, causing pulmonary hypoplasia 1
- Not caused by maternal bleeding events like subchorionic hemorrhage
Diagnosis and Assessment
The diagnosis of CDH at 20 weeks through anatomy scan is consistent with standard practice:
- CT scan is the gold standard for diagnosing diaphragmatic abnormalities in adults, but prenatal ultrasound is the primary diagnostic tool during pregnancy 1, 2
- The finding of intestines in the chest cavity pushing the heart to the right side indicates a severe form of CDH 3
- Severity assessment includes evaluation of:
Prenatal Treatment Options
Fetoscopic Endoluminal Tracheal Occlusion (FETO) is a proven prenatal intervention that could have been considered for this severe CDH case: 3
- FETO involves placing a balloon in the fetal trachea to promote lung growth
- Level I evidence shows FETO increases survival to discharge in selected cases 3
- Typically offered for severe cases with poor predicted outcomes 5
- The procedure has shown a 50% survival rate in severe cases 5
- Timing of the procedure is critical for balancing benefits against risks of prematurity 3
Management of Subchorionic Hemorrhage
Regarding the subchorionic hemorrhage at 15 weeks:
- Standard management typically includes monitoring and sometimes activity restriction
- There is no evidence that specific interventions for subchorionic hemorrhage would have prevented or affected the CDH 1
- The hemorrhage and the CDH are unrelated conditions, as the diaphragm forms much earlier in development
Postnatal Surgical Management
Had the pregnancy continued, postnatal management would have included:
- Immediate intubation and ventilation in a tertiary care center 1
- Surgical repair of the diaphragmatic defect:
Prognosis and Outcomes
The severity of this case (intestines in chest, cardiac displacement) suggests a challenging prognosis:
- Higher risk features include:
- Liver herniation into chest
- Need for patch repair
- Potential need for extracorporeal membrane oxygenation (ECMO) 4
- Prenatal diagnosis and management in specialized centers can improve outcomes despite higher risk factors 4
- Survival rates vary significantly based on severity, with overall survival around 73% in centers with multidisciplinary perinatal management 4
Key Points for Patient Counseling
- CDH is a developmental defect that occurs early in pregnancy, unrelated to the subchorionic hemorrhage
- For severe cases like this, prenatal intervention with FETO could have been considered at specialized centers
- Optimal management requires delivery at a tertiary care center with immediate neonatal support
- Outcomes depend on severity factors, with specialized centers achieving better results even in high-risk cases