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Drug Interactions between exenatide and sevoflurane

This report displays the potential drug interactions for the following 2 drugs:

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Interactions between your drugs

Major

sevoflurane exenatide

Applies to: sevoflurane and exenatide

Consumer information for this interaction is not currently available.

ADJUST DOSING INTERVAL: Treatment with a glucagon-like peptide-1 (GLP-1) receptor agonist or a dual glucose-dependent insulinotropic polypeptide (GIP) and GLP-1 receptor agonist may increase the risk of regurgitation and pulmonary aspiration of gastric contents in patients undergoing general anesthesia due to delayed gastric emptying caused by stimulation of central nervous system GLP-1 receptors and vagal nerve activation. Pulmonary aspiration of regurgitated gastric contents during anesthesia may result in pneumonitis, aspiration pneumonia, other lung injury, and even death. Cases associated with the use of GLP-1 agonists, particularly for the treatment of weight loss, have been documented in the medical literature. There have also been reports of aborted procedures in patients treated with these agents due to the presence of significant residual gastric contents despite adherence to preoperative fasting protocols prior to anesthesia. The effects on gastric emptying may be reduced with long-term use, most likely through rapid tachyphylaxis at the level of vagal nerve activation. Therefore, patients who have recently started treatment with these agents may be at greater risk of delayed gastric emptying and pulmonary aspiration than those who have been taking them for a longer period. Additionally, patients experiencing gastrointestinal (GI) symptoms from these agents, including nausea, vomiting or abdominal distension, have a greater risk of increased residual gastric contents regardless of fasting.

MANAGEMENT: Although data are limited, caution and close monitoring are advisable when general anesthesia or deep sedation is required in patients receiving GLP-1 agonists or dual GIP/GLP-1 agonists. Consideration should be given to withholding these medications prior to the scheduled procedure whenever possible, although the optimal duration of treatment interruption has not been established. The benefits of these medications on glycemic control should also be weighed against the risk of regurgitation and pulmonary aspiration in determining if and for how long these medications should be withheld. For elective procedures, the American Society of Anesthesiologists (ASA) Task Force on Preoperative Fasting suggests pausing the GLP-1 agonist or dual GIP/GLP-1 agonist on the day of the procedure for patients on daily dosing and a week prior to the procedure for patients on weekly dosing. This recommendation is irrespective of the indication (type 2 diabetes mellitus or weight loss) or the type of procedure or surgery. If treatment is suspended for longer than the dosing schedule in patients with diabetes, consult with an endocrinologist on bridging the antidiabetic therapy to avoid hyperglycemia. On the day of the procedure, if GI symptoms such as severe nausea/vomiting/retching, abdominal bloating, or abdominal pain are present, consider delaying elective procedure; otherwise, proceed as usual if the GLP-1 agonist or dual GIP/GLP-1 agonist has been held as advised. If no GI symptoms are present, but the GLP-1 agonist or dual GIP/GLP-1 agonist was not held as advised, proceed with "full stomach" precautions or consider evaluating gastric volume by ultrasound. Patients whose stomach is empty can proceed as usual. For patients whose stomach is full or gastric ultrasound is inconclusive or not possible, consider delaying the procedure or treat the patient as "full stomach" and manage accordingly. Likewise, patients requiring urgent or emergent procedures should be treated as "full stomach" and managed accordingly. Similar guidelines have been provided by the Canadian Anesthesiologists' Society, the main difference being its recommendation that GLP-1 agonists and dual GIP/GLP-1 agonists be held for 3 half-lives (approximately 88% clearance of the drug) in patients receiving these agents for weight management.

Drug and food interactions

Moderate

exenatide food

Applies to: exenatide

You should take exenatide twice a day, at any time within the 60 minutes (1 hour) before your morning and evening meals, or before the two main meals of the day, and at least 6 hours or more apart. You may experience decreased absorption of exenatide in the presence of food or other medications. Your other medications should be administered at least 1 hour before or 2 hours after your exenatide injection.

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Therapeutic duplication warnings

No warnings were found for your selected drugs.

Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.


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Drug Interaction Classification

These classifications are only a guideline. The relevance of a particular drug interaction to a specific individual is difficult to determine. Always consult your healthcare provider before starting or stopping any medication.
Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan.
Unknown No interaction information available.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.