Glycopyrrolate Premedication and Procedure-Related Events in Pediatric Upper Endoscopy

Dmitry Tumin1, Daniel A Ladin2, Matthew Ledoux1,3

  • 1Department of Pediatrics, Brody School of Medicine at East Carolina University, Greenville, NC, USA.

Clinical Pediatrics
|October 10, 2024
PubMed

Insights

Glycopyrrolate premedication in pediatric endoscopy did not reduce overall events but was linked to fewer serious adverse events (SAEs). Further trials are needed to confirm its benefit for reducing severe complications.

Area of Science:

  • Pediatric Gastroenterology
  • Anesthesiology
  • Clinical Pharmacology

Background:

  • Glycopyrrolate is used for pediatric upper endoscopy, but evidence for its effectiveness is limited.
  • The study addresses the need for clinical data on glycopyrrolate's role in pediatric procedural safety.

Purpose of the Study:

  • To determine if glycopyrrolate premedication is associated with a reduced incidence of procedure-related events and serious adverse events (SAEs) in pediatric upper endoscopy.
  • To analyze the safety and efficacy of glycopyrrolate in this specific patient population.

Main Methods:

  • Retrospective analysis of 1046 pediatric upper endoscopy procedures from the Pediatric Sedation Research Consortium registry (April 2020 - February 2022).
  • Primary outcome: incidence of any procedure-related events. Secondary outcome: incidence of SAEs.
  • Multivariable analysis was used to assess the association between glycopyrrolate use and outcomes, controlling for patient and procedural factors.

Main Results:

  • The overall event rate was 15%, with 3% of patients experiencing SAEs.
  • Glycopyrrolate was not significantly associated with the overall event rate (OR: 1.08; 95% CI: 0.72, 1.61).
  • Glycopyrrolate use was associated with significantly lower odds of SAEs (OR: 0.34; 95% CI: 0.13, 0.91).

Conclusions:

  • Glycopyrrolate premedication may reduce the risk of serious adverse events during pediatric upper endoscopy.
  • While the study suggests a potential benefit in reducing SAEs, prospective trials are necessary to validate these findings.
  • Further research is recommended to support the routine clinical use of glycopyrrolate for this indication.

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