What are the latest recommendations for managing Glucagon-like peptide-1 (GLP-1) receptor agonists, such as liraglutide (Victoza) and semaglutide (Ozempic), in patients undergoing anesthesia and surgery?

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Last updated: November 6, 2025View editorial policy

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Latest Recommendations for GLP-1 Receptor Agonists and Anesthesia

Primary Recommendation

For patients taking GLP-1 receptor agonists undergoing elective surgery, hold the medication for at least three half-lives before the procedure (approximately 3 weeks for weekly semaglutide, 3 days for daily liraglutide) to minimize aspiration risk, with specific management strategies based on whether this timeline can be achieved. 1, 2

Preoperative Assessment and Documentation

Before any procedure requiring anesthesia or deep sedation, document the following 1:

  • Specific GLP-1 agent, dose, and indication (diabetes vs. weight loss)
  • Date commenced, last dose taken, and any recent dose changes
  • Presence of gastrointestinal symptoms (nausea, vomiting, abdominal distention)
  • Concomitant medications that delay gastric emptying (opioids, proton pump inhibitors, tricyclic antidepressants)
  • Recent recreational drug use (alcohol, cannabis) that affects gastric motility

Medication Holding Periods by Half-Life

The three half-life rule clears approximately 88% of the drug from the system 1:

  • Weekly agents (semaglutide/Ozempic): Hold for 3 weeks (approximately 21 days) 2
  • Daily agents (liraglutide/Victoza): Hold for 3 days 1

Management Based on Indication

For Weight Loss Patients

Hold GLP-1 receptor agonists for at least three half-lives before elective procedures without exception, as the risks of continuing outweigh benefits in this population 1, 2

For Diabetes Patients

Consult with the treating endocrinologist to weigh glycemic control benefits against aspiration risk 1, 2. This consultation should address:

  • Risks and benefits of holding the drug for three half-lives
  • Bridging diabetic therapy recommendations if the GLP-1 agent must be held longer than the next scheduled dose 1

Risk Stratification and High-Risk Scenarios

Consider patients at high risk for retained gastric contents if they have 1, 2:

  • Unable to hold medication for three half-lives before the procedure
  • Recently started the medication or increased dose (within 12 weeks)
  • Active gastrointestinal symptoms (nausea, vomiting, abdominal distention)

Aspiration Risk Reduction Strategies

For High-Risk Patients

Implement the following evidence-based interventions 1, 2:

  1. Preprocedural diet modification: 24-hour clear fluid diet followed by standard 6-hour fasting 3

  2. Prokinetic medication: Administer metoclopramide or erythromycin preoperatively 1, 2

  3. Point-of-care gastric ultrasound: Assess for residual gastric contents (volume >1.5 ml/kg indicates high risk) 1, 2

  4. Rapid sequence intubation: Use this technique to reduce aspiration risk during induction 1, 2

  5. Pre-emptive gastric decompression: Consider in very high-risk patients 1

  6. Procedure postponement: Reschedule elective cases when possible to allow adequate drug clearance 1

Standard Fasting Times

Standard preoperative fasting times (6 hours for solids, 2 hours for clear liquids) are insufficient for patients on GLP-1 receptor agonists, even after proper fasting, due to delayed gastric emptying 2, 4. The 24-hour clear fluid diet is now recommended 3.

Day of Procedure Algorithm

On the day of surgery, follow this decision pathway 1:

  • If GLP-1 withheld for three half-lives AND no high-risk features: Perform gastric ultrasound

    • If gastric volume <1.5 ml/kg with no solid matter: Proceed with standard anesthetic technique
    • If gastric volume >1.5 ml/kg or solids present: Treat as high-risk (see below)
  • If GLP-1 NOT withheld for three half-lives OR high-risk features present:

    • Administer prokinetic medication
    • Perform gastric ultrasound
    • Use rapid sequence intubation
    • Consider delaying procedure

Evidence Quality and Controversies

The recommendation to hold GLP-1 agents represents a significant shift from earlier guidance 5. Prior to 2023, guidelines recommended continuing these medications perioperatively 1. This change was driven by:

  • Case reports of aspiration events despite proper fasting 2
  • Endoscopic evidence of retained gastric contents in patients on GLP-1 agents 1
  • FDA acknowledgment that available data are insufficient to inform specific recommendations, but pulmonary aspiration has been reported 4

However, one large retrospective study found no increased risk of perioperative complications in GLP-1 users compared to non-users 6. Despite this, the preponderance of mechanistic evidence (delayed gastric emptying) and case reports supports a cautious approach 1, 2.

The Australian/New Zealand 2025 guidelines diverge slightly, recommending continuation of GLP-1 agents with 24-hour clear fluid diet modification rather than cessation 3. However, the three half-life cessation approach from the Anaesthesia journal guidelines represents the most conservative and widely adopted international standard 1, 2.

Critical Pitfalls to Avoid

  • Do not rely on absence of gastrointestinal symptoms to rule out retained gastric contents; aspiration has occurred in asymptomatic patients 2, 3
  • Do not assume standard fasting times are adequate even if the medication was held for only 1 week (the older ASA recommendation) 2
  • Do not forget to inform patients preoperatively to notify healthcare providers about GLP-1 use before any planned procedures 4
  • Do not discontinue GLP-1 agents in diabetic patients without endocrinology consultation regarding bridging therapy 1, 2

Shared Decision-Making

Use a transparent discussion approach with patients to explain the aspiration risk, the rationale for holding medications, and alternative management strategies, allowing informed consent for the chosen approach 1.

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Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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