Evaluating bowel obstruction and ileus events in patients on GLP-1 receptor agonists: a systematic review and meta-analysis.
Expert Opin Drug Saf · 2025
Last updated 2026-05-28A review of 14 studies involving over 550,000 people found that GLP-1 drugs as a group did not raise the risk of bowel obstruction or ileus compared to controls (odds ratio 1.95, 95% confidence interval 0.43–8.79). However, one specific drug, liraglutide, showed a higher risk (odds ratio 3.0, 95% confidence interval 2.03–4.45) than semaglutide.
AI summary of the abstract below.
| Journal | Expert Opin Drug Saf, 2025 |
|---|---|
| Citations | 5 |
| Relative citation ratio | 2.18 |
| Molecules | — |
Abstract
INTRODUCTION: This research evaluated the association between glucagon-like peptide-1 receptor agonists (GLP-1 RA) and bowel obstruction or ileus.
METHODS: We searched databases, including Medline, Embase, and Cochrane, for studies on adult patients treated with GLP-1 RA. We included randomized control trials (RCT), cohort, case-control studies, and case reports. We used the Cochrane Risk of Bias tool to evaluate the quality of RCTs and the Newcastle-Ottawa Scale for cohort and case-control studies.
RESULTS: Out of 317 records identified, 14 studies were included in the systematic review. The meta-analysis included 6 studies with a combined total of 550,426 participants. The use of GLP-1 RA did not show an incremental risk of bowel obstruction or ileus compared to controls (OR 1.95, 95% CI 0.43-8.79). However, the studies had high heterogeneity (I = 94%). A subgroup analysis by specific medication revealed that liraglutide was associated with a significantly high risk of bowel obstruction or ileus (OR 3.0, 95% CI 2.03-4.45; I = 0%).
CONCLUSIONS: GLP-1 receptor agonists do not significantly increase the risk of bowel obstruction or ileus. However, liraglutide is associated with a higher risk compared to semaglutide. Clinicians should remain aware of these rare events while recognizing the benefits of GLP-1 receptor agonists for glycemic control and cardiovascular health.
PROSPERO REGISTRATION: CRD42024585971.
Verbatim abstract via PubMed 39964295 ↗