Long-gap esophageal atresia

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Esophageal atresia is a rare congenital anomaly that occurs in 1 in 4,500 live births. The expected outcome is close to 100% survival, though this varies depending on birth weight, degree of prematurity, and associated anomalies (especially cardiac). Ideal surgical management consists of a primary end-to-end anastomosis between the upper and the lower esophageal remnants and division of a tracheo-esophageal fistula, if one is present. The vast majority can be corrected without difficulty soon after birth. However, this goal is not always easily achievable with all anatomical variants and the management of long-gap esophageal atresia remains a major challenge to the pediatric surgeon. In addition, there is controversy regarding the definition of a long gap and a general lack of consensus regarding which is the best technique. This is perhaps due to the fact that attempts to bridge the gap to allow a delayed anastomosis have led to the introduction of several interesting techniques, none of which are perfect.

Original languageEnglish
Title of host publicationFundamentals of Pediatric Surgery
PublisherSpringer New York
Pages233-246
Number of pages14
ISBN (Print)9781441966421
DOIs
Publication statusPublished - 2011

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ASJC Scopus subject areas

  • Medicine(all)

Cite this

Bagolan, P., & Morini, F. (2011). Long-gap esophageal atresia. In Fundamentals of Pediatric Surgery (pp. 233-246). Springer New York. https://doi.org/10.1007/978-1-4419-6643-8_30