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Published on: February 5, 2021
Vascular and pulmonary comorbidities in children with congenital EA/TEF
Thomas S Poore1,2, Jason P Weinman2,3, Elyse Handley4
1Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.
Insights
Computed tomography (CT) and CT angiography (CTA) reveal frequent vascular abnormalities and tracheal compression in patients with esophageal atresia with tracheoesophageal fistula (EA/TEF). These findings aid in managing persistent respiratory symptoms.
Area of Science:
- Pediatric radiology
- Thoracic imaging
- Congenital anomalies
Background:
- Esophageal atresia with tracheoesophageal fistula (EA/TEF) is often associated with congenital and vascular malformations.
- Limited studies have utilized computed tomography (CT) and CT angiography (CTA) to investigate these associations.
- This study reviews CT findings in patients with EA/TEF to identify pulmonary and vascular abnormalities.
Purpose of the Study:
- To review CT scans of the chest in patients diagnosed with EA/TEF.
- To report pulmonary and vascular findings associated with EA/TEF.
- To assess the utility of CT and CTA in evaluating airway mechanics and comorbidities.
Main Methods:
- Retrospective chart review of pediatric patients with EA/TEF.
- Analysis of the most recent chest CT or CTA results.
- Recording of demographics, medical conditions, bronchoscopy findings, and measurement of tracheal lumen area ratio on CTA.
Main Results:
- 47 patients with EA/TEF had available chest CT scans.
- Bronchiectasis was present in 8% of patients.
- Vascular abnormalities were identified in 58% of contrast CT scans, and 62% demonstrated tracheal compression.
- Tracheomalacia was evaluated using expiratory:inspiratory tracheal area ratio (mean 0.57).
Conclusions:
- Patients with EA/TEF frequently exhibit vascular abnormalities impacting airway mechanics and pulmonary comorbidities.
- CT angiography should be considered as an adjunct to bronchoscopy for persistent respiratory symptoms.
- These imaging findings are crucial for optimizing medical and surgical management in children with EA/TEF.
Background:
Esophageal atresia with tracheoesophageal fistula (EA/TEF) is associated with many congenital and vascular malformations; however, reports utilizing computed tomography (CT) and computed tomography angiography (CTA) are limited. The objective of this study is to review CT scans of the chest from patients with EA/TEF and report their pulmonary and vascular findings.
Methods:
We completed a retrospective chart review of children with congenital EA/TEF evaluated in the aerodigestive clinic at Children's Hospital Colorado. Results of the most recent CTA or CT of the chest were investigated. Demographics, medical conditions, and bronchoscopy findings were also recorded. The ratio of tracheal lumen area between inspiratory and expiratory CTA images was measured.
Results:
Of the patients with congenital EA/TEF seen in the program, 47 patients had a chest CT available for review. Eight patients (17%) had bronchiectasis. Of the contrast CT scans, 15 (58%) had a vascular abnormality and 16 (62%) demonstrated tracheal compression (38% at the level of the innominate artery, 35% from other structures). Nineteen of the CTAs had volumetric expiratory images of the trachea to evaluate tracheomalacia. The mean expiratory:inspiratory area was 0.57 (SD ± 0.23) at the level of the innominate.
Conclusion:
Patients with EA/TEF frequently have vascular abnormalities that may alter airway mechanics as well as pulmonary comorbidities that may affect long-term management. For patients experiencing persistent respiratory symptoms, CTA of the chest should be considered adjunct to bronchoscopy to help with medical and surgical management of these children.
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