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Review
. 2017 Nov 25;19(12):65.
doi: 10.1007/s11894-017-0605-6.

How to Care for Patients with EA-TEF: The Known and the Unknown

Affiliations
Review

How to Care for Patients with EA-TEF: The Known and the Unknown

Hayat Mousa et al. Curr Gastroenterol Rep. .

Abstract

Purpose of review: Guidelines were recently published highlighting why esophageal atresia (EA) patients are prone to complication risks, and the need for long-term follow-up. In this review, we will focus on how to investigate and treat potential complications, as well as the pros and cons of different investigative and treatment modalities, and what areas continue to need further research.

Recent findings: EA patients are at high risk for gastroesophageal reflux and esophageal strictures, and the sequela that result. Extraintestinal manifestations of gastroesophageal reflux disease (GERD) can appear similar to other pathologic diagnoses commonly found in EA patients, such as congenital stricture, eosinophilic esophagitis, esophageal dysmotility, tracheomalacia, recurrent fistula, aspiration, etc. Therefore, it is important to have a standardized way to monitor for these issues. pH impedance allows for detection of nonacid reflux and the height of reflux, which are important in correlating symptoms with reflux episodes. A multidisciplinary approach is beneficial in evaluating and monitoring EA patients in the long term.

Keywords: Anastamotic strictures; Complications; Eosinophilic esophagitis; Esophageal atresia; Gastroesophageal reflux disease; Long-term follow-up; Multichannel intraluminal impedance; Review; Tracheoesophageal fistula.

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References

    1. Shaw-Smith C, Oesophageal atresia, tracheo-oesophageal fistula, and the VACTERL association: review of genetics and epidemiology. J Med Genet, 2006. 43(7): p. 545–54. - PMC - PubMed
    1. Demikova NS, et al., Prevalence and descriptive epidemiology of esophageal atresia in the Russian Federation. Birth Defects Res A Clin Mol Teratol, 2016. 106(10): p. 854–859. - PubMed
    1. Nassar N, et al., Prevalence of esophageal atresia among 18 international birth defects surveillance programs. Birth Defects Res A Clin Mol Teratol, 2012. 94(11): p. 893–9. - PMC - PubMed
    1. Cassina M, et al., Prevalence, characteristics, and survival of children with esophageal atresia: A 32-year population-based study including 1,417,724 consecutive newborns. Birth Defects Res A Clin Mol Teratol, 2016. 106(7): p. 542–8. - PubMed
    1. Donoso F, et al., Outcome and management in infants with esophageal atresia - A single centre observational study. J Pediatr Surg, 2016. 51(9): p. 1421–5. - PubMed

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