Literature DB >> 16903645

Esophageal atresia with tracheoesophageal fistula: ten years of experience in an institute.

Chia-Feng Yang1, Wen-Jue Soong, Mei-Jy Jeng, Shu-Jen Chen, Yu-Sheng Lee, Pei-Chen Tsao, Betau Hwang, Chou-Fu Wei, Tai-Wai Chin, Chinsu Liu.   

Abstract

BACKGROUND: Esophageal atresia (EA), tracheoesophageal fistula (TEF), or both is a complicated problem. The purpose of this study was to evaluate the outcomes and postoperative complications in patients with EA/TEF who were admitted to our hospital.
METHODS: In total, 15 patients were enrolled from 1994 to 2003, including 8 males and 7 females. Patient demographics, associated anomalies, and outcomes were analyzed.
RESULTS: The most common variant was EA with a distal TEF (type C), which occurred in 12 patients (80%). The latter had associated congenital anomalies, and cardiac anomalies were the most frequent, occurring in 8 patients (53.3%). Of the 6 cases who had life-threatening anomalies, 4 (66.7%) died, and of the 9 cases who had no life-threatening-anomalies, 2 (22.2%) died. Tracheomalacia and/or stenosis were diagnosed in 8 patients (66.7%) postoperatively. Though 3 of the 4 cases who suffered from dying spell received intratracheal stent implantation, 2 cases still died.
CONCLUSION: The survival rate of the patients with EA/TEF is influenced mainly by associated life-threatening anomalies. TMS combined with a history of dying spell may be the major fatal complication.

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Year:  2006        PMID: 16903645     DOI: 10.1016/S1726-4901(09)70265-5

Source DB:  PubMed          Journal:  J Chin Med Assoc        ISSN: 1726-4901            Impact factor:   2.743


  6 in total

1.  The role of prophylactic chest drainage in the operative management of esophageal atresia with tracheoesophageal fistula.

Authors:  Saeid Aslanabadi; Masoud Jamshidi; R Shane Tubbs; Mohammadali Mohajel Shoja
Journal:  Pediatr Surg Int       Date:  2009-03-17       Impact factor: 1.827

Review 2.  VACTERL anomalies in patients with esophageal atresia: an updated delineation of the spectrum and review of the literature.

Authors:  Scott J Keckler; Shawn D St Peter; Patricia A Valusek; Kuojen Tsao; Charles L Snyder; George W Holcomb; Daniel J Ostlie
Journal:  Pediatr Surg Int       Date:  2007-02-15       Impact factor: 1.827

3.  Spinal dysraphism as a new entity in V.A.C.TE.R.L syndrome, resulting in a novel acronym V.A.C.TE.R.L.S.

Authors:  Aymeric Amelot; Célia Cretolle; Timothée de Saint Denis; Sabine Sarnacki; Martin Catala; Michel Zerah
Journal:  Eur J Pediatr       Date:  2020-02-13       Impact factor: 3.183

Review 4.  Current knowledge on esophageal atresia.

Authors:  Paulo Fernando Martins Pinheiro; Ana Cristina Simões e Silva; Regina Maria Pereira
Journal:  World J Gastroenterol       Date:  2012-07-28       Impact factor: 5.742

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

Authors:  Saeid Aslanabadi; Kamyar Ghabili; Mohsen Rouzrokh; Mohammad Bagher Hosseini; Masoud Jamshidi; Farzad Hami Adl; Mohammadali M Shoja
Journal:  Int J Gen Med       Date:  2011-06-23

6.  Efficacy and Safety of Endoscopic Esophageal Dilatation in Pediatric Patients with Esophageal Strictures.

Authors:  Hasan M A Isa; Khadija A Hasan; Husain Y Ahmed; Afaf M Mohamed
Journal:  Int J Pediatr       Date:  2021-09-24
  6 in total

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