Peripherally acting μ-opioid receptor antagonists for treatment of opioid-induced constipation in children

Chris Novak1,2, Amanda Hogg1,2, Kyle Sue1,2

  • 1Stollery Children's Hospital, Edmonton, Alberta.

Insights

Peripherally acting mu-opioid receptor antagonists (PAMORAs) like methylnaltrexone and naloxegol effectively treated opioid-induced constipation in hospitalized children. Most patients experienced a bowel movement within 24 hours with no significant adverse events.

Area of Science:

  • Pediatric pharmacology
  • Gastroenterology
  • Palliative care

Background:

  • Opioid-induced constipation (OIC) is a prevalent issue in pediatric critical care, palliative, and postoperative settings.
  • Current OIC treatments are often limited by enteral intake and may be ineffective.
  • Peripherally acting mu-opioid receptor antagonists (PAMORAs), such as methylnaltrexone and naloxegol, offer a novel therapeutic approach.

Purpose of the Study:

  • To evaluate the effectiveness and safety of methylnaltrexone and naloxegol for OIC in hospitalized children.
  • To assess PAMORA efficacy in pediatric patients, including those with critical illness.

Main Methods:

  • A retrospective study was conducted at Stollery Children's Hospital, Edmonton, Canada.
  • Included were all pediatric patients who received methylnaltrexone or naloxegol for OIC.
  • The primary outcome measured was the median time to the first bowel movement (BM) post-PAMORA administration.

Main Results:

  • Twenty-seven pediatric patients were included in the analysis.
  • The median time to the first BM after PAMORA initiation was 15.5 hours.
  • Sixty-three percent of patients achieved laxation within 24 hours; no significant adverse events were reported.

Conclusions:

  • This study represents the largest evaluation of PAMORA efficacy and safety in pediatric patients to date.
  • Findings suggest PAMORAs are a safe and effective treatment option for OIC in hospitalized children.
  • Future research should focus on prospective studies with larger cohorts, particularly for critically ill and postoperative pediatric patients experiencing OIC.
Abstract

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