Small intestinal bacterial overgrowth in children with intestinal failure on home parenteral nutrition

Kathleen H McGrath1,2, James Pitt3,4, Julie E Bines1,2,3

  • 1Department of Gastroenterology and Clinical Nutrition The Royal Children's Hospital Melbourne Victoria Australia.

Insights

Children with intestinal failure (IF) on home parenteral nutrition (PN) frequently experience small intestinal bacterial overgrowth (SIBO). Symptoms vary by IF cause, and diagnosis is challenging, necessitating further research into surrogate markers.

Area of Science:

  • Pediatric Gastroenterology
  • Intestinal Failure Research
  • Microbiome Studies

Background:

  • Children with intestinal failure (IF) exhibit altered gut anatomy/function, predisposing them to small intestinal bacterial overgrowth (SIBO).
  • Home parenteral nutrition (PN) is a common supportive therapy for IF, but may influence SIBO risk.
  • Accurate diagnosis of SIBO in this vulnerable population presents significant challenges.

Purpose of the Study:

  • To describe clinical features of clinically suspected SIBO in children with IF on home PN.
  • To review diagnostic testing challenges for SIBO in pediatric IF.
  • To explore potential novel diagnostic surrogate markers for SIBO in this cohort.

Main Methods:

  • A single-center, retrospective chart review of all clinically suspected SIBO episodes over 33 months.
  • Data collection included clinical symptoms and diagnostic tests performed.
  • Patient characteristics, including IF etiology (short bowel syndrome vs. non-SBS IF), were recorded.

Main Results:

  • 71% of children on home PN experienced at least one episode of clinically suspected SIBO.
  • Short bowel syndrome (SBS) and non-SBS IF each accounted for 50% of cases.
  • Diarrhea was the most frequent symptom, particularly in SBS patients, with non-SBS IF patients reporting more symptoms per episode.

Conclusions:

  • Children with IF on home PN represent a high-risk group for SIBO.
  • SIBO clinical presentations are variable and can overlap with underlying IF symptoms.
  • Clinical suspicion is crucial due to diagnostic test limitations; further research into surrogate markers like urinary metabolite screens is warranted.
Abstract

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