A. Nawaz et al., Esophageal atresia and tracheoesophageal fistula: success and failure rates in the United Arab Emirates, PEDIAT SURG, 14(3), 1998, pp. 214-217
The management of esophageal atresia (EA) and tracheoesophageal fistula (TE
F) has improved markedly over the years, with a current overall survival of
80%-90%. This however, is not the case in developing countries, where mort
ality continues to be high. The results of treatment of 41 consecutive case
s EA and/or TEF have been analyzed to determine factors pertinent to the ou
tcome. The distribution of anomalies and a postoperative survival of 86.8%
were comparable to those from developed countries. Aspiration pneumonia was
unusually frequent in our patients (78%), but did not adversely influence
outcome. Associated congenital anomalies as well as low birth weight contin
ue to be important predictors of outcome in our setting. Our post-operative
complications were similar to those from developed countries apart from a
high incidence of stricture formation. This was attributed to gastroesophag
eal reflux, non-ventilation post-operatively, and the use of silk sutures t
o construct the anastomosis.