Eur J Pediatr Surg 2024; 34(01): 044-049
DOI: 10.1055/a-2123-5026
Original Article

Esophageal Atresia Associated with Congenital Duodenal Obstruction: Turkish Esophageal Atresia Registry (TEAR) Evaluation

Authors

  • Çiğdem Ulukaya Durakbaşa

    1   Department of Pediatric Surgery, Istanbul Medeniyet University Faculty of Medicine, Istanbul, Turkey
    2   Department of Pediatric Surgery, Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Istanbul, Turkey
  • Tutku Soyer

    3   Department of Pediatric Surgery, Hacettepe University Faculty of Medicine, Ankara, Turkey
  • Hüseyin İlhan

    4   Department of Pediatric Surgery, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey
  • Mustafa Onur Oztan

    5   Department of Pediatric Surgery, Izmir Katip Celebi University, Izmir, Turkey
  • Osman Uzunlu

    6   Department of Pediatric Surgery, Pamukkale University, Denizli, Turkey
  • Binali Firinci

    7   Department of Pediatric Surgery, Ataturk University School of Medicine, Erzurum, Turkey
  • Rahşan Özcan

    8   Department of Pediatric Surgery, Istanbul University-Cerrahpasa Cerrahpasa Faculty of Medicine, Istanbul, Turkey
  • Akgun Oral

    9   Department of Pediatric Surgery, Dr. Behcet Uz Child Disease and Surgery Training and Research Hospital, Izmir, Turkey
  • Ilhan Ciftci

    10   Department of Pediatric Surgery, Selcuklu Medical Faculty, University of Selcuk, Konya, Turkey
  • Esra Ozcakir

    11   Department of Pediatric Surgery, Bursa Yuksek Ihtisas Training and Research Hospital, Bursa, Turkey
  • Ibrahim Akkoyun

    12   Department of Pediatric Surgery, Konya Training and Research Hospital, Konya, Turkey
  • Doğuş Güney

    13   Department of Pediatric Surgery, Ankara Yildirim Beyazit University Faculty of Medicine, Ankara, Turkey
  • Onder Ozden

    14   Department of Pediatric Surgery, Cukurova University Faculty of Medicine, Adana, Turkey
  • Cengiz Gul

    15   Department of Pediatric Surgery, Istanbul Zeynep Kamil Maternity and Children's Diseases Health Training and Research Center, University of Health Sciences, Istanbul, Turkey
  • Coskun Ozcan

    16   Department of Pediatric Surgery, Ege University, Izmir, Turkey
  • Ayse Parlak

    17   Department of Pediatric Surgery, Bursa Uludag University Medical Faculty, Bursa, Turkey
  • Emrah Aydın

    18   Department of Pediatric Surgery, Tekirdag Namik Kemal Universitesi, Tekirdag, Turkey

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