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Abstract
No significant risk differences were found for acute pancreatitis or biliary disease in patients treated with glucagon-like peptide-1 receptor agonists (GLP-1 RA) compared to sodium-glucose cotransporter 2 inhibitors (SGLT-2i).
- The hazard ratio for acute pancreatitis in patients treated with GLP-1 RA was 0.56, indicating no increased risk.
- The hazard ratio for biliary disease was 1.12, suggesting no significant difference in risk between the two treatment groups.
- Secondary analyses confirmed the lack of risk differences for both acute pancreatitis and biliary disease.
- Adherence to approved treatment indications and monitoring for adverse events is recommended for patient safety.
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