Impact of Surgical Diaphragmatic Repair on Central Airway Shape in Neonatal Congenital Diaphragmatic Hernia

Chamindu C Gunatilaka1, Sahr Alisher2, Margo Waters3

  • 1Division of Pulmonary Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.

Pediatric Pulmonology
|February 12, 2026
PubMed

Insights

Congenital diaphragmatic hernia (CDH) in neonates often involves persistent central airway issues like tracheobronchomalacia. Ultrashort echo time MRI reveals these airway abnormalities may worsen after surgical repair, suggesting underdiagnosis.

Area of Science:

  • Pediatric Surgery
  • Radiology
  • Neonatal Medicine

Background:

  • Neonates with congenital diaphragmatic hernia (CDH) frequently exhibit central airway abnormalities, such as tracheobronchomalacia, which can persist post-surgical repair.
  • These airway complications are often underdiagnosed due to reliance on symptomatic evaluation and limited use of bronchoscopy.
  • Ultrashort echo time (UTE) magnetic resonance imaging (MRI) provides a non-invasive, 3D method for assessing airway dynamics and evaluating tracheobronchomalacia.

Purpose of the Study:

  • To quantify changes in central airway morphology and dynamics before and after surgical diaphragmatic repair in neonates with CDH using UTE MRI.
  • To assess the utility of UTE MRI in identifying and characterizing airway abnormalities in neonates with CDH.

Main Methods:

  • Retrospective analysis of neonates with CDH who underwent pre- and post-surgical UTE MRI between 2015 and 2020.
  • Respiratory-gated radial 3D UTE images acquired at four breathing phases to assess airway dynamics.
  • Generation of 3D airway surfaces from the cricoid to the main bronchi for analysis of cross-sectional areas, dynamic collapse, and eccentricity index.

Main Results:

  • Six neonates with left-sided CDH were included in the study.
  • Post-surgery, a significant decrease in tracheal minimum eccentricity index (indicating increased collapse) was observed (0.68 to 0.53, p=0.023).
  • The ipsilateral bronchus also showed significant changes with decreased eccentricity index (0.65 to 0.55, p=0.048), while the contralateral bronchus remained stable. Tracheal cross-sectional area decreased, and dynamic motion increased post-surgery.

Conclusions:

  • Neonates with CDH exhibit significant central airway abnormalities pre-surgery that persist or worsen post-repair, particularly in the trachea and ipsilateral bronchus.
  • These findings highlight tracheobronchomalacia as an underrecognized component of CDH.
  • Integrating airway assessment into surgical planning may improve post-operative outcomes for neonates with CDH.
Abstract