Airway management

Glucagon-like peptide-1 receptor agonists and impaired gastric emptying: a pharmacovigilance analysis of the US Food and Drug Administration adverse event reporting system

Br J AnaesthPublished Pharmacovigilance study

Authors' conclusion

GLP-1RAs were notably associated with reports of impaired gastric emptying in the FAERS.

Study context

Population
Adverse event reports of impaired gastric emptying (IGE) in the US FDA Adverse Event Reporting System (FAERS), 2004 Q1 to 2024 Q1IGE cases, top 10 drugs
Participants
1,982 participants
Outcome
Association between GLP-1RAs and impaired gastric emptying (IGE) reports
Methodological detailsdisproportionality analysis of the FAERS database, reporting odds ratio, logistic regression, Kaplan-Meier and Weibull shape parameter tests
  • Disproportionality analysis of the FAERS database
  • Reporting odds ratio
  • Logistic regression
  • Kaplan-Meier and Weibull shape parameter tests

Main finding

As reported in the abstract

GLP-1RAs among top 10 drugs linked to IGE reports

GLP-1RAs among top 10 drugs associated with IGE reports

5

Proportion of IGE cases accounted for by GLP-1RAs

49.5%

982/1982

Observational data: associations, not effects.

Further findings

Older age and IGE risk, dulaglutide

OR (95% CI)P value
Older ageLower IGE risk with older age0.97 (0.94–1.00)P = 0.033

Older age and IGE risk, semaglutide

OR (95% CI)P value
Older ageLower IGE risk with older age0.96 (0.94–0.97)P = 0.001

Higher weight and IGE risk, exenatide

OR (95% CI)P value
Higher weightLower IGE risk0.99 (0.98–1.00)P = 0.033

Male sex and IGE risk, exenatide

OR (95% CI)P value
Male sexLower IGE risk0.39 (0.20–0.68)P = 0.033

Median time to IGE onset from initiation of therapy

  • Median time to IGE onset from initiation of therapy: range of median onset times across GLP-1RAs

Weibull shape parameter β

β <1 for all GLP-1RAs, indicating higher IGE risk early in treatment

Original publication

Glucagon-like peptide-1 receptor agonists and impaired gastric emptying: a pharmacovigilance analysis of the US Food and Drug Administration adverse event reporting system. Br J Anaesth. Published 21 November 2024. doi:10.1016/j.bja.2024.10.013

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