OESOPHAGEAL ATRESIA (EA)
AND TRACHEO-OESOPHAGEAL
FISTULA (TEF)
Anjali Babu
KCON
• Esophageal atresia is the failure of
esophagus to form a continuous passage
from the pharynx to the stomach.
• Type A: pure esophageal atresia with no
TEF, about 8% of EA patients have this
type .
• Type B: EA with proximal TEF , or a TEF
connecting between the upper pouch of
the esophagus and trachea. Rare,0.8% of
patients have this.with this type food and
saliva can travel directly into the lungs
before surgical correction is performed.
• Type C: EA with a distal TEF ,or TEF connecting
between the lower pouch of the esophagus and
the trachea. Commonest type with about 89%
0f patients have this. With this type gastric
contents and acid can travel directly into the
lungs before correction is performed.
• Type D: EA with dual TEF ,Where there is both a
TEF connecting between the upper pouch of
esophagus and the trachea , and a TEF
connecting the lower pouch of the esophagus
and the trachea. Rare only 1.4% of EA patients
have this.
• Type E/ H- type: H-type TEF where there is
TEF connecting between the esophagus
and the trachea but there is no EA.
children with an H-type TEF , unlike other
types ,are often diagnosed later in infancy or
childhood ,rather than becoming evident
shortly after birth.
Child with H-type can swallow but often
cough and choke during swallowing ,
especially with liquids, and may present with
recurrent pneumonias.