Oesophageal atresia
Abstract
Although the overall survival rate for infants with oesophageal atresia now exceeds 90%, the condition continues to be responsible for significant morbidity, mainly as a consequence of associated congenital anomalies of which cardiac malformations (29%) are most prominent. A recently revised risk classification comprising very low birth weight (<1500 g) and/or major cardiac defects more accurately predicts survival in the modern era. Early complications following repair include anastomotic leaks, strictures and recurrent fistula, while late complications comprise tracheomalacia causing acute life-threatening attacks, gastrooesophageal reflux, and respiratory and oesophageal motility disorders.
Keywords: oesophageal atresia, tracheo-oesophageal fistula
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- f1 E-mail: L.spitz@ich.ucl.ac.uk
PII: S0957-5839(01)90187-3
doi:10.1054/cupe.2001.0187
© 2001 Harcourt Publishers Ltd. All rights reserved.

