Associated congenital anomalies between neonates with short-gap and long-gap esophageal atresia: a comparative study

• Published in: International journal of general medicine 2011-01, Vol.4 (default), p.487-491
• Main Authors: Aslanabadi, Saeid, Ghabili, Kamyar, Rouzrokh, Mohsen, Hosseini, Mohammad Bagher, Jamshidi, Masoud, Adl, Farzad Hami, Shoja, Mohammadali M
• Format: Article
• Language: English
• Subjects: anomaly; Defects; esophageal atresia; Esophagus; long-gap; Original Research; short-gap; tracheoesophageal fistula; VACTERL
• ISSN: 1178-7074; 1178-7074
• DOI: 10.2147/IJGM.S19301

Predicting the presence of long-gap esophageal atresia (EA) prior to the surgery is of clinical importance. No comparison between short-gap and long-gap EA for the prevalence of VACTERL and non-VACTERL-type anomalies has yet been performed. The aim of this study was to compare VACTERL and non-VACTERL-type anomalies between patients with short-gap and long-gap EA. Retrospectively, medical records of all newborns managed for EA/tracheoesophageal fistula (TEF) in Tabriz Children's Hospital and Tehran Mofid Hospital between 2007 and 2010 were evaluated. Demographic data and associated anomalies including both the VACTERL and non-VACTERL-type defects were listed. The VACTERL spectrum defects covered vertebral/costal, anorectal, cardiovascular, TEF, and renal- or radial-type limb anomalies. The non-VACTERL-type anomalies included hydrocephalus, orofacial defects, respiratory system anomalies, gastrointestinal anomalies, genital anomalies, and non-VACTERL limb defects. Demographic data, and the VACTERL and non-VACTERL-type anomalies were compared among children with long-gap EA and those with short-gap EA. Two hundred and seventy-six children were included in the study: 230 (83.3%) in the short-gap EA group and 46 (16.7%) in the long-gap EA group. Although prevalence of the VACTERL spectrum anomalies did not differ between the two groups, the non-VACTERL anomaly was more common in the long-gap EA group (P = 0.02). Among the VACTERL-type defects, TEF was detected in 30 (65.2%) and 218 (94.7%) patients in long-gap and short-gap EA groups, respectively (P = 0.0001). The non-VACTERL-type anomalies, but not the VACTERL spectrum defects, are more frequent in patients with long-gap EA than those with short-gap EA.