Literature DB >> 15213904

Long gap esophageal atresia and esophageal replacement: moving toward a separation?

P Bagolan1, B d Iacobelli Bd, P De Angelis, G Federici di Abriola, R Laviani, A Trucchi, M Orzalesi, L Dall'Oglio.   

Abstract

BACKGROUND/
PURPOSE: Treatment of long gap esophageal atresia (EA) is still a major challenge. Gastric transposition and colon interposition are the 2 most popular choices for esophageal replacement, but there is general agreement that the child's own esophagus is the best. The aim of the study was to critically evaluate the feasibility and outcome of primary repair of long gap EA with or without tracheoesophageal fistula (TEF) by direct esophago-esophageal anastomosis as the only technique.
METHODS: Seventy-one neonates with EA+/-TEF were considered. Nineteen cases were classified as long gap (> or =3 cm). All infants underwent either primary or shortly delayed repair. In the latter group, a gastrostomy was performed along with an x-ray evaluation of the gap a few days before surgery (mean age, 46.4 days). To avoid disruptive anastomotic force, all infants were kept paralyzed and mechanically ventilated for an additional 6 days after esophageal anastomosis. Before starting feeding, postoperative esophagogram was done on day 7. Endoscopy was done routinely, starting 1 month after surgery; pH monitoring was conventionally performed at 1 year of age or even earlier, should gastroesophageal reflux disease (GERD) be suspected. Follow-up ranged from 11 months to 7 years.
RESULTS: In all 19 long gap EA infants an esophago-esophageal anastomosis was performed. Six of them (31%) required an anterior esophageal flap to bridge residual gap. Complications included minor anastomotic leak in 2 cases and anastomotic stricture (<5mm) in 12 (80%) cases, which were treated with an average of 5 dilatations (1 of which with resection of the stricture). GERD occurred in 8 cases (53.3%), of which, 3 required fundoplication. None of the patients had esophageal swallowing difficulties or persistent dysphagia. Two children experienced food aversion. Mean hospital stay was 66.2 (22 to 230) days. There were 4 deaths (very low birth weight, 1; associated anomalies, 1; and late sepsis, 2).
CONCLUSIONS: Considering heat gap determination remains imprecise, it seems possible to conclude that in a well-established tertiary care level referral center: (1) long gap EA could be treated successfully with primary repair and anastomosis; (2) strictures and GER represent the most frequent postoperative problem, but additional procedures required seem "acceptable" to maintain the patient's own esophagus and avoid replacement; (3) esophageal substitution in long gap EA should be reserved for cases in which a previous attempt of esophageal reconstruction failed.

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Year:  2004        PMID: 15213904     DOI: 10.1016/j.jpedsurg.2004.03.048

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  16 in total

1.  Retrosternal revision of jejunum interposed in the anterior sternal space for the treatment of esophageal atresia.

Authors:  Chizue Ichijo; Tadaharu Okazaki; Masaaki Oshita; Toshihiro Yanai; Geoffrey J Lane; Atsuyuki Yamataka
Journal:  Pediatr Surg Int       Date:  2007-10       Impact factor: 1.827

Review 2.  Delayed primary anastomosis for management of long-gap esophageal atresia: a meta-analysis of complications and long-term outcome.

Authors:  Florian Friedmacher; Prem Puri
Journal:  Pediatr Surg Int       Date:  2012-09       Impact factor: 1.827

3.  Comparison of outcomes of thoracoscopic primary repair of gross type C esophageal atresia performed by qualified and non-qualified surgeons.

Authors:  Yujiro Tanaka; Takahisa Tainaka; Wataru Sumida; Chiyoe Shirota; Naruhiko Murase; Kazuo Oshima; Ryo Shirotsuki; Kosuke Chiba; Hiroo Uchida
Journal:  Pediatr Surg Int       Date:  2017-08-11       Impact factor: 1.827

4.  Repair of esophageal atresia with proximal fistula using endoscopic magnetic compression anastomosis (magnamosis) after staged lengthening.

Authors:  Robert M Dorman; Kaveh Vali; Carroll M Harmon; Mario Zaritzky; Kathryn D Bass
Journal:  Pediatr Surg Int       Date:  2016-03-24       Impact factor: 1.827

5.  Prognosis of congenital tracheoesophageal fistula with esophageal atresia on the basis of gap length.

Authors:  Vijay D Upadhyaya; A N Gangopadhyaya; D K Gupta; S P Sharma; Vijayendra Kumar; Anand Pandey; Ashish D Upadhyaya
Journal:  Pediatr Surg Int       Date:  2007-06-20       Impact factor: 1.827

6.  Preservation of native esophagus in infants with pure esophageal atresia has good long-term outcomes despite significant postoperative morbidity.

Authors:  Augusto Zani; Giovanni Cobellis; Justyna Wolinska; Priscilla P L Chiu; Agostino Pierro
Journal:  Pediatr Surg Int       Date:  2015-10-31       Impact factor: 1.827

Review 7.  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

8.  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

9.  Comparison of outcomes according to the operation for type A esophageal atresia.

Authors:  Yeon-Ju Huh; Hyun-Young Kim; Seong-Cheol Lee; Kwi-Won Park; Sung-Eun Jung
Journal:  Ann Surg Treat Res       Date:  2014-01-22       Impact factor: 1.859

10.  Repair of long-gap esophageal atresia: gastric conduits may improve outcome-a 20-year single center experience.

Authors:  Catherine J Hunter; Mikael Petrosyan; Meghan E Connelly; Henri R Ford; Nam X Nguyen
Journal:  Pediatr Surg Int       Date:  2009-12       Impact factor: 1.827

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