Subscribe to RSS
DOI: 10.1055/a-2123-5026
Esophageal Atresia Associated with Congenital Duodenal Obstruction: Turkish Esophageal Atresia Registry (TEAR) Evaluation
Abstract
Introduction Coexistent congenital duodenal obstruction and esophageal atresia (EA) is known to have significant morbidity and mortality. Management strategies are not well-defined for this association. The data from the Turkish EA registry is evaluated.
Materials and Methods A database search was done for the years 2015 to 2022.
Results Among 857 EA patients, 31 (3.6%) had congenital duodenal obstruction. The mean birth weight was 2,104 (± 457) g with 6 babies weighing less than 1,500 g. Twenty-six (84%) had type C EA. The duodenal obstruction was complete in 15 patients and partial in 16. Other anomalies were detected in 27 (87%) patients. VACTERL-H was present in 15 (48%), anorectal malformation in 10 (32%), a major cardiac malformation in 6 (19%), and trisomy-21 in 3 (10%). Duodenal obstruction diagnosis was delayed in 10 (32%) babies for a median of 7.5 (1–109) days. Diagnosis for esophageal pathologies was delayed in 2. Among 19 babies with a simultaneous diagnosis, 1 died without surgery, 6 underwent triple repair for tracheoesophageal fistula (TEF), EA, and duodenal obstruction, and 3 for TEF and duodenal obstruction in the same session. A staged repair was planned in the remaining 9 patients. In total, 15 (48%) patients received a gastrostomy, the indication was long-gap EA in 8. Twenty-five (77%) patients survived. The cause of mortality was sepsis (n = 3) and major cardiac malformations (n = 3).
Conclusion Congenital duodenal obstruction associated with EA is a complex problem. Delayed diagnosis is common. Management strategies regarding single-stage repairs or gastrostomy insertions vary notably depending on the patient characteristics and institutional preferences.
Publication History
Received: 02 May 2023
Accepted: 04 July 2023
Accepted Manuscript online:
05 July 2023
Article published online:
09 August 2023
© 2023. Thieme. All rights reserved.
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
-
References
- 1 Miscia ME, Lauriti G, Di Renzo D, Riccio A, Lisi G, Lelli Chiesa P. Esophageal atresia and associated duodenal atresia: a cohort study and review of the literature. Eur J Pediatr Surg 2021; 31 (05) 445-451
- 2 Stark Z, Patel N, Clarnette T, Moody A. Triad of tracheoesophageal fistula-esophageal atresia, pulmonary hypoplasia, and duodenal atresia. J Pediatr Surg 2007; 42 (06) 1146-1148
- 3 Dave S, Shi EC. The management of combined oesophageal and duodenal atresia. Pediatr Surg Int 2004; 20 (09) 689-691
- 4 Spitz L, Ali M, Brereton RJ. Combined esophageal and duodenal atresia: experience of 18 patients. J Pediatr Surg 1981; 16 (01) 4-7
- 5 Ein SH, Palder SB, Filler RM. Babies with esophageal and duodenal atresia: a 30-year review of a multifaceted problem. J Pediatr Surg 2006; 41 (03) 530-532
- 6 Fragoso AC, Ortiz R, Hernandez F, Olivares P, Martinez L, Tovar JA. Defective upper gastrointestinal function after repair of combined esophageal and duodenal atresia. J Pediatr Surg 2015; 50 (04) 531-534
- 7 Ceccanti S, Midrio P, Messina M. et al. The DATE association: a separate entity or a further extension of the VACTERL association?. J Surg Res 2019; 241: 128-134
- 8 Nabzdyk CS, Chiu B, Jackson CC, Chwals WJ. Management of patients with combined tracheoesophageal fistula, esophageal atresia, and duodenal atresia. Int J Surg Case Rep 2014; 5 (12) 1288-1291
- 9 Spitz L, Kiely EM, Morecroft JA, Drake DP. Oesophageal atresia: at-risk groups for the 1990s. J Pediatr Surg 1994; 29 (06) 723-725
- 10 Holder TM, Ashcraft KW, Sharp RJ, Amoury RA. Care of infants with esophageal atresia, tracheoesophageal fistula, and associated anomalies. J Thorac Cardiovasc Surg 1987; 94 (06) 828-835
- 11 Soyer T, Öztorun Cİ, Fırıncı B. et al. The effect of azygos vein preservation on postoperative complications after esophageal atresia repair: results from the Turkish Esophageal Atresia Registry. J Pediatr Surg 2021; 56 (11) 1940-1943
- 12 Oztan MO, Soyer T, Oztorun CI. et al. Outcome of very low and low birth weight infants with esophageal atresia: results of the Turkish Esophageal Atresia Registry. Eur J Pediatr Surg 2021; 31 (03) 226-235