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Evolving Approaches to Congenital Diaphragmatic Hernia Management
Abby C Larson1,2, Jason Gien3, S Christopher Derderian1,2
1Division of Pediatric Surgery, Department of Surgery, University of Colorado School of Medicine, Aurora, Colorado.
Insights
Congenital diaphragmatic hernia (CDH) management has improved survival rates to 75-90% in mild/moderate cases. This review covers CDH care from prenatal diagnosis to survivorship, highlighting emerging advancements for better outcomes.
Area of Science:
- Pediatric Surgery
- Neonatology
- Developmental Biology
Background:
- Congenital diaphragmatic hernia (CDH) is a complex birth defect impacting lung and heart development.
- Pulmonary hypoplasia and abnormal pulmonary vasculature are key features of CDH.
- Despite challenges, survival rates have improved due to advances in neonatal care and surgical techniques.
Purpose of the Study:
- To synthesize current evidence on the comprehensive management of congenital diaphragmatic hernia (CDH).
- To review the entire continuum of care for CDH patients, from prenatal diagnosis to long-term survivorship.
- To identify emerging areas and future directions in CDH research and clinical practice.
Main Methods:
- Comprehensive literature review of contemporary evidence on congenital diaphragmatic hernia (CDH).
- Synthesis of data across the full spectrum of CDH care, including prenatal, perinatal, and postnatal management.
- Identification and discussion of novel diagnostic and therapeutic strategies, such as fetal intervention and precision medicine.
Main Results:
- Survival rates for isolated mild to moderate congenital diaphragmatic hernia (CDH) cases approach 75% to 90%.
- Advances in neonatal intensive care, specialized centers, and surgical timing have significantly improved outcomes.
- Key management areas include prenatal diagnosis, fetal intervention (FETO), postnatal stabilization, ECMO, surgical repair, and long-term care.
Conclusions:
- Contemporary management strategies have markedly improved survival for congenital diaphragmatic hernia (CDH) patients.
- Future advancements lie in precision prenatal risk stratification, refined fetal interventions like FETO, standardized guidelines for ECMO and surgery, and integrated multidisciplinary care models.
- Optimizing long-term outcomes and survivorship requires a continued focus on evidence-based, coordinated care.
Abstract:
Congenital diaphragmatic hernia (CDH) is a complex developmental anomaly characterized by pulmonary hypoplasia, abnormal pulmonary vascular development, and variable cardiac dysfunction. Due to advances in neonatal intensive care, center expertise, and surgical repair after physiologic stability, mortality has improved over the past few decades, with survival rates in isolated mild to moderate cases approaching 75% to 90%. This review synthesizes contemporary evidence across the continuum of care for CDH: prenatal diagnosis and imaging; fetal intervention, including fetoscopic endoluminal tracheal occlusion (FETO); delivery planning; postnatal stabilization; ventilatory and hemodynamic management; extracorporeal membrane oxygenation (ECMO); surgical repair; postoperative care; chronic morbidity; and survivorship. Emerging areas include precision prenatal risk stratification, refinement of FETO, harmonized ECMO and surgical guidelines, and long-term multidisciplinary models of care.
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