GLP-1 agonists

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Background

  • Synthetic glucagon-like peptide-1 (GLP-1) receptor agonists
  • Released by L-cells of the small intestine in response to the presence of nutrients
  • Stimulate insulin release from pancreatic islet cells. It does this by stimulating glucose-dependent insulin release in the islet cells of the pancreas
  • Slows gastric emptying times
  • Increases satiety, which decreases drive for food intake

GLP-1 Agonist Types

Drug (Brand) Class Dose Route Frequency Key Indications
Daily Dosing
Exenatide (Byetta) GLP-1 RA (exendin-4 based) 5-10 mcg SC BID T2DM
Lixisenatide (Adlyxin) GLP-1 RA (exendin-4 based) 10-20 mcg SC Daily T2DM
Liraglutide (Victoza) GLP-1 RA (human GLP-1 based) 0.6-1.8 mg SC Daily T2DM, CV risk reduction
Liraglutide (Saxenda) GLP-1 RA (human GLP-1 based) 3.0 mg SC Daily Obesity/overweight
Weekly Dosing
Semaglutide (Ozempic) GLP-1 RA (human GLP-1 based) 0.25-2 mg SC Weekly T2DM, CV risk reduction, CKD
Semaglutide (Wegovy) GLP-1 RA (human GLP-1 based) 0.25-2.4 mg SC Weekly Obesity/overweight, CV risk reduction
Semaglutide (Rybelsus) GLP-1 RA (human GLP-1 based) 3-14 mg PO Daily T2DM
Semaglutide (Wegovy Pill) GLP-1 RA (human GLP-1 based) 1.5-25 mg PO Daily Obesity/overweight
Dulaglutide (Trulicity) GLP-1 RA (human GLP-1 based) 0.75-4.5 mg SC Weekly T2DM, CV risk reduction
Tirzepatide (Mounjaro) Dual GLP-1/GIP RA 2.5-15 mg SC Weekly T2DM
Tirzepatide (Zepbound) Dual GLP-1/GIP RA 2.5-15 mg SC Weekly Obesity/overweight, OSA
  • Albiglutide (Tanzeum) — discontinued 2017 (commercial reasons, not safety); removed from table
  • Exenatide ER (Bydureon BCise) — discontinued 2023; brand Byetta discontinued 2024 (generic exenatide available)

ED-Relevant Considerations

  • Delayed gastric emptying — all GLP-1 RAs slow gastric motility; important for:
    • Aspiration risk during procedural sedation and intubation (consider NPO status unreliable)
    • Altered absorption of co-administered oral medications
    • 2023 ASA guidance recommends holding GLP-1 RAs prior to elective procedures requiring anesthesia
  • Pancreatitis — rare but serious; discontinue if pancreatitis confirmed
  • Hypoglycemia — low risk as monotherapy; increased risk when combined with sulfonylurea or insulin
  • Nausea/vomiting — most common adverse effect; dose-dependent, typically improves with time
  • Injection site reactions — generally mild
  • Cholelithiasis/cholecystitis — increased incidence reported
  • Contraindicated in personal/family history of medullary thyroid carcinoma or MEN type 2

Indication

Adverse Reactions

  • Nausea, vomiting, diarrhea
  • Acute pancreatitis
  • Exenatide should not be used in patients with creatinine clearance below 30mL/min
  • Should not be used if personal of family history of medullary thyroid cancer or MEN 2A/2B

See Also

References

  1. Epocrates
  2. http://www.uptodate.com/contents/glucagon-like-peptide-1-receptor-agonists-for-the-treatment-of-type-2-diabetes-mellitus?source=see_link&sectionName=GLUCAGON-LIKE+PEPTIDE-1&anchor=H2#H619400