Related Experiment Video
Updated: Feb 13, 2026

Laparoscopic Repair of Para-Esophageal Hernia Using Absorbable Biosynthetic Mesh
Published on: September 11, 2021
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.
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.
Rationale:
Neonates with congenital diaphragmatic hernia (CDH) frequently experience central airway abnormalities, including tracheobronchomalacia, which persist post-surgical repair. However, these complications often remain underdiagnosed due to reliance on symptomatic evaluation and limited use of bronchoscopy. Ultrashort echo time (UTE) magnetic resonance imaging (MRI) offers a non-invasive, three-dimensional method to assess airway dynamics and evaluate tracheobronchomalacia.
Objectives:
To quantify changes in central airway morphology and dynamics before and after surgical diaphragmatic repair in neonates with CDH using UTE MRI.
Methods:
This study examined neonates with CDH admitted between 2015 and 2020 who underwent both pre- and post-surgical UTE MRI. Airway dynamics were assessed using respiratory-gated radial three-dimensional UTE images at four breathing phases. Three-dimensional airway surfaces were generated from the cricoid to the main bronchi. Changes from pre- to post-surgery in cross-sectional areas, dynamic collapse, and eccentricity index were analyzed.
Results:
Six neonates with left-sided CDH were included. Following surgery, tracheal minimum eccentricity index at end expiration decreased significantly (0.68 ± 0.06 to 0.53 ± 0.15, p = 0.023), indicating increased collapse. The ipsilateral bronchus demonstrated similar changes, with eccentricity index decreasing significantly from 0.65 ± 0.04 to 0.55 ± 0.11 (p = 0.048), while the contralateral bronchus remained stable. Mean tracheal cross-sectional area decreased from 22.7 ± 6.1 mm² to 19.1 ± 3.1 mm² (p = 0.115), while dynamic motion increased from 21 ± 7% to 40 ± 15% (p = 0.055).
Conclusions:
Neonates with CDH have significant central airway abnormalities pre-surgery, which persists and may worsen post-repair, particularly in the trachea and ipsilateral bronchus. These findings suggest tracheobronchomalacia is an underrecognized component of CDH. Integrating airway assessment into surgical planning could improve post-operative outcomes.
Related Concept Videos
VSEPR Theory and the Basic Shapes
Mismatch Repair
Overview of DNA Repair
Chemically...
Base Excision Repair
The first step of...
The Central Dogma
Nucleotide Excision Repair

