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SOMNATH MAITY
INTERN
It is an abnormal connection between the
trachea and the esophagus.
 1 in 3500 births
 Male predominance.
 common in prematurity.
 50% with associated anomalies.
 Cardiac anomalies.( 14.8 – 24 %)
 First pregnancy
 age of mother < 20 years
 Elderly mothers.
 Multiple births.
 Trisomy 18 ( Edward’s Syndrome)
Upper part of esophagus develops from retro-
pharyngeal segment of primitive gut and the
lower part from the first part.
At 4-5 weeks of gestation, a laryngo-tracheal
groove is formed and divides the foregut into
two longitudinal furrows.
Respiratory tract is then separated from the
esophagus.
Defective separation due to deviated or
incomplete septum or due incomplete fusion
of tracheal folds result in fistula formation
between the trachea and the esophagus.
 Excessive salivation and constant drooling of
saliva from the mouth.
 Violent response during feeding : (3 C s)
• Coughing
• Chocking
• Cyanosis
 Fluid returns through the mouth and nostrils.
 Frothy salivation.
 Abdominal distension in types C, D, E.
 Aspiration Pneumonia.
1. Prenatal
2. Postnatal
PRENATAL :
a) USG : reveals polyhydramnios, absence of
fluid filled stomach, a small abdomen,
and a distended esophageal pouch.
b) Fetal MRI: Confirmatory.
Postnatal:
• X-Rays: done using radio opaque catheter in
the esophagus to check for obstructions.
• Bronchoscopy: shows fistula between trachea
and esophagus.
• Inability to pass nasogastric tube due to
resistance.
PREOPERATIVE MEASURES
 Attention to the respiratory status of the infant.
 Positioning of infant.
 Decompression of the upper pouch
 Appropriate timing of surgery
 Passing of a nasogastric tube.
 Presence of other associated anomalies like
congenital cardiac disease.
 NPM, TPN.
 Upper pouch suction.
 IV antibiotics.
 IV fluids.
 Surgery :- Definitive Treatment
 Timothy Holmes(1869) first suggested
surgical anastomosis.
 Charles Steelle (1888) first surgical attempt.
 Esophago-esophagostomy : Thoracotomy
Thoracoscopy
Staging Surgery
 1st Stage: TEF ligated and gastrostomy is
done to reduce the risk of reflux to provide
feeding.
 2nd Stage: Both proximal and distal segments
are anastomosed. And if the gap is too large
then a segment of it is used for
reconstruction of the esophagus at 18-24
months.
 IV Fluids continuing.
 Provide oxygen
 Feeding orally or through Gastrostomy.
 Analgesics if required.
 Tracheomalacia.
 Dysphagia.
 Esophageal strictures.
 Respiratory Distress.
 GERD.
 Aspiration pnemonitis with
pneumonia .
 Esophageal diverticula.
 Esophageal strictures.
 Esophagitis.
 GERD.
Tracheo oesophageal fistula

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Tracheo oesophageal fistula

  • 2. It is an abnormal connection between the trachea and the esophagus.
  • 3.  1 in 3500 births  Male predominance.  common in prematurity.  50% with associated anomalies.  Cardiac anomalies.( 14.8 – 24 %)
  • 4.  First pregnancy  age of mother < 20 years  Elderly mothers.  Multiple births.  Trisomy 18 ( Edward’s Syndrome)
  • 5. Upper part of esophagus develops from retro- pharyngeal segment of primitive gut and the lower part from the first part. At 4-5 weeks of gestation, a laryngo-tracheal groove is formed and divides the foregut into two longitudinal furrows. Respiratory tract is then separated from the esophagus.
  • 6. Defective separation due to deviated or incomplete septum or due incomplete fusion of tracheal folds result in fistula formation between the trachea and the esophagus.
  • 7.
  • 8.  Excessive salivation and constant drooling of saliva from the mouth.  Violent response during feeding : (3 C s) • Coughing • Chocking • Cyanosis  Fluid returns through the mouth and nostrils.  Frothy salivation.  Abdominal distension in types C, D, E.  Aspiration Pneumonia.
  • 9.
  • 10. 1. Prenatal 2. Postnatal PRENATAL : a) USG : reveals polyhydramnios, absence of fluid filled stomach, a small abdomen, and a distended esophageal pouch. b) Fetal MRI: Confirmatory.
  • 11.
  • 12. Postnatal: • X-Rays: done using radio opaque catheter in the esophagus to check for obstructions. • Bronchoscopy: shows fistula between trachea and esophagus. • Inability to pass nasogastric tube due to resistance.
  • 13.
  • 14.
  • 15.
  • 16. PREOPERATIVE MEASURES  Attention to the respiratory status of the infant.  Positioning of infant.  Decompression of the upper pouch  Appropriate timing of surgery  Passing of a nasogastric tube.  Presence of other associated anomalies like congenital cardiac disease.  NPM, TPN.  Upper pouch suction.  IV antibiotics.  IV fluids.
  • 17.  Surgery :- Definitive Treatment  Timothy Holmes(1869) first suggested surgical anastomosis.  Charles Steelle (1888) first surgical attempt.  Esophago-esophagostomy : Thoracotomy Thoracoscopy
  • 18.
  • 19. Staging Surgery  1st Stage: TEF ligated and gastrostomy is done to reduce the risk of reflux to provide feeding.  2nd Stage: Both proximal and distal segments are anastomosed. And if the gap is too large then a segment of it is used for reconstruction of the esophagus at 18-24 months.
  • 20.  IV Fluids continuing.  Provide oxygen  Feeding orally or through Gastrostomy.  Analgesics if required.
  • 21.  Tracheomalacia.  Dysphagia.  Esophageal strictures.  Respiratory Distress.  GERD.
  • 22.  Aspiration pnemonitis with pneumonia .  Esophageal diverticula.  Esophageal strictures.  Esophagitis.  GERD.