Congenital Diaphragmatic Hernia — Research Summary
Printed from RareWays (rareways.com.au) on 12 September 2026
For general awareness only. Not medical advice. Discuss all care options with your healthcare team.
5 Most Recent Research Articles
- 1.
A Simplified Surgical Technique for Thoracoscopic Repair of Congenital Diaphragmatic Hernia.
Wang Jiepin et al. — Journal of laparoendoscopic & advanced surgical techniques. Part A (1 October 2026)
https://pubmed.ncbi.nlm.nih.gov/42091573/
- 2.
Meta-analysis of prostacyclin therapy for persistent pulmonary hypertension with congenital diaphragmatic hernia.
Jiang Shouliang et al. — Journal of pediatric surgery (1 October 2026)
https://pubmed.ncbi.nlm.nih.gov/42492725/
- 3.
Cardiac morphology in children at 2 and 10 years of age after congenital diaphragmatic hernia repair: a comparative MRI-based analysis of ECMO and non-ECMO patients.
Jawhar Schanas et al. — European radiology (9 September 2026)
https://pubmed.ncbi.nlm.nih.gov/42711441/
- 4.
Historical evolution of thoracoscopic repair for congenital diaphragmatic hernia: an era-based systematic review and meta-analysis.
Yamoto Masaya et al. — Surgical endoscopy (9 September 2026)
https://pubmed.ncbi.nlm.nih.gov/42717045/
- 5.
Minimally Invasive Transabdominal Repair of Incarcerated Morgagni Hernia in Adults.
Bova Kailey et al. — Journal of laparoendoscopic & advanced surgical techniques. Part A (7 September 2026)
https://pubmed.ncbi.nlm.nih.gov/42704346/
Clinical Trials — Australian Sites
Ask your doctor whether you or your child may be eligible for any of these trials.
- 1.
Physiological-based Cord Clamping in Congenital Diaphragmatic Hernia
Active (not recruiting) — Na — Erasmus Medical Center
https://clinicaltrials.gov/study/NCT04373902
- 2.
Tracheal Occlusion To Accelerate Lung Growth (TOTAL) Trial for Severe Pulmonary Hypoplasia
Completed — Phase 2 — University Hospital, Gasthuisberg
https://clinicaltrials.gov/study/NCT01240057
- 3.
Fetal Surgery for Moderate Left Sided Congenital Diaphragmatic Hernia.
Completed — Na — University Hospital, Gasthuisberg
https://clinicaltrials.gov/study/NCT00763737
Source: RareWays research directory. Data from PubMed, Europe PMC, OpenAlex, ClinicalTrials.gov.
Always verify information with your healthcare team before making any decisions about your care.
Congenital Diaphragmatic Hernia
Congenital diaphragmatic hernia is a rare birth defect in which the muscle separating the chest and abdomen does not close fully, letting abdominal organs move into the chest and limiting lung growth. Babies often have breathing difficulty from birth. Care involves stabilising breathing and circulation, then surgery to repair the opening, with ongoing follow-up.
Most Recent Research
INTRODUCTION: The current surgical approaches for treating congenital diaphragmatic hernia (CDH) are challenging. Thoracoscopic transcutaneous closure of CDH is described, of which a retrospective study was conducted to investigate the safety and effectiveness. MATERIALS AND METHODS: In thoracoscopic transcutaneous closure, a thoracoscope and operating forceps are placed through two intercostal ports to expose the defect, followed by stepwise thoracic pressure elevation to facilitate herniated organ reduction. A fascial closure device is introduced through a small skin incision to encircle the diaphragmatic rim in two semicircular passes, and the suture is then tightened extracorporeally to close the defect. RESULTS: Over a 8-year period, 33 TTC repairs were performed for CDH, including 31 Bochdalek and 2 Morgagni cases. Bochdalek repairs were completed in a mean operative time of 53.68 ± 45.81 minutes (range, 10-200 minutes), with a median age of 1 day and median weight of 3.25 kg. Among them, two patients experienced recurrence at 3 months and 7 months postoperatively. During hospitalization, four patients developed pneumothorax, and one patient developed chylothorax. The two Morgagni cases were repaired in 35 and 30 minutes at 5 and 6 months of age. Respiratory support was a median of 59 hours (range, 0-352 hours) in patients who required respiratory assistance, intensive care unit stay was a median of 15 days (range, 1-91 days) in patients admitted to the intensive care unit, and hospital stay was a median of 15 days (range, 2-91 days). All patients had uneventful wound healing without rib-development complications during follow-up. CONCLUSION: Thoracoscopic transcutaneous closure is a feasible and effective technique to treat CDH. While possessing the advantages of minimally invasive surgery, it shortens the operative time and learning curve.
Common Questions
What is Congenital Diaphragmatic Hernia?
Congenital diaphragmatic hernia is a rare birth defect in which the muscle separating the chest and abdomen does not close fully, letting abdominal organs move into the chest and limiting lung growth. Babies often have breathing difficulty from birth. Care involves stabilising breathing and circulation, then surgery to repair the opening, with ongoing follow-up.
How many clinical trials are available for Congenital Diaphragmatic Hernia?
RareWays currently indexes 72 clinical trials for Congenital Diaphragmatic Hernia, of which 28 are actively recruiting. Trial availability changes as new studies are registered — check the trials tab for current status.
Where does the research data for Congenital Diaphragmatic Hernia come from?
RareWays aggregates research from PubMed, Europe PMC, OpenAlex, and ClinicalTrials.gov. Data is updated regularly by Rocky, RareWays' automated research engine. All articles and trials link directly to their original sources.
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