This site is intended for healthcare professionals

Go to /sign-in page

You can view 5 more pages before signing in

Tracheoesophageal fistula

Authoring team

A tracheoesophageal fistula is a connection between the trachea and oesophagus, usually as a result of a failure of normal development.

Tracheoesophageal fistula is generally associated with oesophageal atresia

Oesophageal atresia is a congenital abnormality occurring with an incidence of about 1 in 2500 live births.

  • in the United States, the prevalence is estimated to be 2.3 per 10,000 live births (1)

The oesophagus develops as a derivative of the foregut, from the floor of where the larynx and trachea become separated by the laryngo-tracheal groove.

  • failure of separation or complete development of this foregut tube can lead to tracheo - oesophageal fistula (TOF) and oesophageal atresia (OA)
    • oesophageal atresia presents in neonates as excessive drooling, choking, and failure to pass a nasogastric tube
    • infants with TOF classically present with respiratory distress, feeding difficulties, choking, and risk for aspiration (2)

It is often associated with a tracheo-oesophageal fistula.

There different types of oesophageal atresia:

  • Type A oesophageal atresia
    • isolated oesophageal atresia without associated tracheo-oesophageal fistula and has a prevalence of 8%
  • Type B oesophageal atresia
    • oesophageal atresia with a proximal tracheo-oesophageal fistula
    • the rarest with a prevalence of 1%
  • Type C oesophageal atresia
    • is the most prevalent at 84%
    • a proximal oesophageal atresia with distal tracheo oesophageal fistula
  • Type D oesophageal atresia
    • is oesophageal atresia with both a proximal and distal tracheo - oesophageal atresia
    • is rare at 3% of cases
  • Type E esophageal atresia (H-type fistula) (2)
    • an isolated tracheoesophageal fistula without associated oesophageal atresia
    • prevalence around 4%

Oeosophageal atresia has a high incidence in mothers with polyhydramnios - as high as 85% - and should always be excluded in the baby of mothers with this condition.

Notes:

  • approximately 50% of patients with TOF/EO will have associated congenital anomalies including:
    • VACTERL syndrome (vertebral defects, anal atresia, cardiac defects, TEF, renal anomalies, and limb abnormalities) or
    • CHARGE syndrome (coloboma, heart defects, atresia choanae, growth retardation, genital abnormalities, and ear abnormalities)

Reference:

  • Baldwin D, Yadav D. Esophageal Atresia. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2022 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK560848/
  • Salik I, Paul M. Tracheoesophageal Fistula. In: StatPearls. StatPearls Publishing, Treasure Island (FL); 2021. PMID: 30570997.

Create an account to add page annotations

Annotations allow you to add information to this page that would be handy to have on hand during a consultation. E.g. a website or number. This information will always show when you visit this page.

The content herein is provided for informational purposes and does not replace the need to apply professional clinical judgement when diagnosing or treating any medical condition. A licensed medical practitioner should be consulted for diagnosis and treatment of any and all medical conditions.

Connect

Copyright 2024 Oxbridge Solutions Limited, a subsidiary of OmniaMed Communications Limited. All rights reserved. Any distribution or duplication of the information contained herein is strictly prohibited. Oxbridge Solutions receives funding from advertising but maintains editorial independence.