In this case report we discuss the anaesthetic management of newborns with
esophageal atresia classified as Vogt mb. This type is characterised by an
upper esophageal pouch which ends blindly and a distal tracheoesophageal fi
stula. Commonly associated diseases are cardiac, renal, vertebral and anal
anomalies. The most important intraoperative anaesthesiological complicatio
ns are acidosis, hypoxaemia, gastric distension, endotracheal tube obstruct
ion, tracheal compression, cardiac arrhythmias and atelectasis. In the pres
ented case an endotracheal tube obstruction with hypercapnia occurred which
required a change of the airway. After changing the endotracheal tube the
newborn could be ventilated sufficiently. Further postoperative course was
uneventful.