Oesophageal atresia: at-risk groups for the 1990s

J Pediatr Surg. 1994 Jun;29(6):723-5. doi: 10.1016/0022-3468(94)90354-9.

Abstract

The authors analyzed the outcome for 357 infants with oesophageal atresia and 15 with H-type tracheoesophageal fistula treated from 1980 through 1992. Survival according to Waterston risk categories was 99% for group A, 95% for group B, and 71% for group C. Presently, with optimal management, virtually all infants in groups A and B should survive. When examining the risk factors in the infants who died, two criteria were found to be important predictors of outcome: birth weight of less than 1,500 g and the presence of major congenital cardiac disease. A new classification for predicting outcome in oesophageal atresia is proposed: group I: birth weight > or = 1,500 g, without major cardiac disease, survival 97% (283 of 293); group II: birth weight < 1,500 g, or major cardiac disease, survival 59% (41 of 70); and group III: birth weight < 1,500 g, and major cardiac disease, survival 22% (2 of 9).

MeSH terms

  • Abnormalities, Multiple
  • Birth Weight
  • Cause of Death
  • Esophageal Atresia / mortality*
  • Esophageal Atresia / surgery
  • Heart Defects, Congenital / complications
  • Humans
  • Infant
  • Infant, Newborn
  • Risk Factors
  • Survival Rate
  • Tracheoesophageal Fistula / congenital
  • Tracheoesophageal Fistula / mortality
  • Tracheoesophageal Fistula / surgery