Post-operative colonic manometry in children with Hirschsprung disease: A systematic review

Hannah M E Evans-Barns1,2,3, Justina Swannjo3, Misel Trajanovska1,2,3

  • 1Department of Paediatric Surgery, The Royal Children's Hospital, Melbourne, Victoria, Australia.

Insights

Children with Hirschsprung disease (HD) often have bowel issues after surgery. This review found limited evidence on colonic manometry for assessing motility problems in these patients.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Medical Device Technology

Background:

  • A significant number of children experience persistent bowel dysfunction, including constipation and fecal incontinence, after surgical repair of Hirschsprung disease (HD).
  • Underlying colonic and/or anorectal dysmotility is suspected as the cause of these ongoing symptoms.
  • Colonic manometry is a potential diagnostic tool to investigate gastrointestinal motility patterns in this patient population.

Purpose of the Study:

  • To evaluate the equipment and protocols used for colonic manometry in assessing children post-operative Hirschsprung disease.
  • To summarize existing evidence on colonic motility patterns in children with repaired Hirschsprung disease.

Main Methods:

  • A systematic review of multiple databases (Cochrane Library, Embase, MEDLINE, PubMed) was conducted from January 1, 1980, to March 9, 2020.
  • Studies involving post-operative assessment of children with Hirschsprung disease using colonic manometry were included, adhering to PRISMA guidelines.
  • Data extraction was performed independently by two authors.

Main Results:

  • Five studies met the inclusion criteria, encompassing a total of 496 children, with 184 undergoing colonic manometry.
  • Significant heterogeneity was observed in study populations, manometry equipment, and protocols, limiting direct comparisons.
  • All included studies utilized low-resolution colonic manometry.

Conclusions:

  • There is a notable lack of evidence regarding colonic dysmotility in children following surgical repair of Hirschsprung disease.
  • Current research is constrained by variable methodologies, diverse patient cohorts, and the absence of high-resolution manometry techniques.
Abstract

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