StayCurrentMD · Esophageal morbidity in patients following repair of esophageal atresia: A systematic review
Article1 min read·Published Oct 2020Older

Esophageal morbidity in patients following repair of esophageal atresia: A systematic review

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Article · Oct 2020 · 1 min read

In brief

In brief

Systematic review of 4,882 patients reveals high complication rates following esophageal atresia repair, with 78% experiencing esophageal dysmotility and nearly half developing GERD or dysphagia. Findings emphasize the need for standardized long-term follow-up protocols given improved survival rates and extended timeframes for morbidity development.

Written by the GCMD Library team from the article.

Abstract

Background

Esophageal atresia (EA) is a life-threatening congenital condition, affecting one in 2600 newborns. Morbidity remains high, with many patients experiencing complications, including anastomotic leak/stricture, and gastro-esophageal reflux disease (GERD). Increased understanding of esophageal motility patterns may help explain the etiology of these complications.

Aims

We aimed to review knowledge regarding esophageal motility and related complications in children with EA, evaluate patients' symptomatology and relate this to esophageal motility.

Methods

We performed a systematic review (PROSPERO: CRD42018092277), according to the PRISMA protocol. Two investigators independently conducted search strategies (OvidMEDLINE, PubMed, Cochrane Review, BMJ BestPractice), identifying complications in patients following EA repair. Rates of esophageal dysmotility, GERD, dysphagia, anastomotic leak, anastomotic stricture, recurrent fistula formation, and esophagitis were sought.

Results

A total of 65 publications met selection criteria (n = 4882). Rates of morbidity were high: esophageal dysmotility (78%), GERD (43%), dysphagia (44%), anastomotic leak (19%), anastomotic stricture (26%), recurrent fistula formation (7%), and esophagitis (47%). No correlation appeared to exist with severity of symptoms.

Conclusions

This systematic review identified high rates of complications in children with EA, with esophageal dysmotility present in the majority of patients. Increasing survival, with resultant longer timeframes to develop morbidities, makes standardized follow-up regimens crucial.

Type of study

Prognosis study.

Level of evidence

Level 3.

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