GLP-1 medicines before surgery, anesthesia and colonoscopy: what each medical society says

Quick answer. Medical societies do not all say the same thing about GLP-1 medicines around surgery, anesthesia and colonoscopy. A 2024 US multisociety guidance says most people can continue and calls for steps to lower the chance of stomach contents reaching the lungs. An earlier American Society of Anesthesiologists statement from 2023 suggested considering a hold. UK, Australian, New Zealand and Korean statements also favor continuing. FDA labels report rare aspiration cases and say the data cannot show whether stopping would help. This page reports what each says. It does not tell anyone whether to hold or continue, because that is a decision for the person and their own care team.
Why anesthesia and endoscopy teams ask about GLP-1 medicines
GLP-1 medicines slow how fast the stomach empties. That is part of why people feel full for longer. It also means food or liquid can still be in the stomach after the usual fasting time before a procedure. Anesthesia and sedation relax the muscles that normally keep stomach contents down, so there is a small chance that this material travels into the windpipe and lungs. Doctors call that pulmonary aspiration. It is rare.
The same question comes up for upper endoscopy and colonoscopy, where sedation is common and a stomach that has not emptied can block the view or force the team to stop. The bodies below each tried to answer one question: what, if anything, should change around a procedure for someone who uses one of these medicines. They did not all land in the same place.
This page reports what each body says and what the studies under them found. It does not tell anyone to hold, continue or change a medicine. That decision belongs to the person and their own surgical, anesthesia and prescribing teams. For the same reason the page gives no hold schedule beyond what a named body has printed. The semaglutide and tirzepatide page explains how the medicines work, and questions to ask your prescriber has a list for the appointment.
What the FDA labels say
Ozempic, Wegovy, Zepbound and Mounjaro carry the same warning under the heading "Pulmonary aspiration during general anesthesia or deep sedation". In the parts of the labels the Atlas read, it makes four points.
- The medicine delays gastric emptying.
- There have been rare reports after the medicines reached the market of pulmonary aspiration in people having elective surgery or procedures that needed general anesthesia or deep sedation, including cases where stomach contents were still present despite reported adherence to fasting advice.
- The available data are not enough to say how to lower that risk, including whether changing fasting advice or temporarily stopping the medicine would reduce retained stomach contents.
- Prescribers are told to instruct patients to tell their healthcare providers about the medicine before any planned surgery or procedure.
| Medicine | Warnings section | Label version the Atlas read |
|---|---|---|
| Ozempic (semaglutide) | 5.10 | 5/2026 |
| Wegovy (semaglutide) | 5.10 | 6/2026 |
| Zepbound (tirzepatide) | 5.9 | 8/2026 |
| Mounjaro (tirzepatide) | 5.9 | 8/2026 |
The Ozempic and Mounjaro patient-counseling sections add that the medicine may make the stomach empty more slowly, which may lead to complications with anesthesia or deep sedation during planned procedures. The Atlas did not read that section of the Wegovy and Zepbound labels. One Wegovy label covers the injection and the tablets, and this warning names Wegovy without separating the two. In the parts the Atlas read, none of the labels tells patients to stop the medicine or to continue it. Labels change, so check the current text on DailyMed.
What each medical body says
The table runs from oldest to newest. Each row paraphrases the body's own document. Most of the bodies wrote for elective procedures, and the UK statement says its advice may fit less well in emergencies.
| Body and date | Who it covers | What it says |
|---|---|---|
| American Society of Anesthesiologists (ASA) consensus guidance, June 29, 2023 | Adults and children having elective procedures, whatever the reason for the medicine | For daily medicines, consider holding on the day of the procedure. For weekly ones, consider holding a week before. If the medicine was not held and there are no symptoms, the guidance calls for full-stomach precautions or says to consider a stomach ultrasound if the clinician is proficient with it. If the scan shows a full stomach or is unclear, it says to consider delaying or to treat the patient as having a full stomach. With stomach symptoms on the day, consider delaying an elective procedure. Urgent cases go ahead and are treated as a full stomach. The ASA page now points to the more recent multisociety guidance below. |
| American Gastroenterological Association (AGA) rapid clinical practice update on endoscopy, published November 2023 | Upper and lower endoscopy | With standard fasting and no nausea, vomiting, indigestion or bloating, the update advises proceeding. If symptoms suggest stomach contents are still there, rapid-sequence intubation can be considered where a delay could cause harm. A liquid diet the day before a sedated procedure may be a more acceptable strategy than stopping the medicine. |
| Multisociety guidance from five societies, October 29, 2024 | Adults having elective surgery or GI endoscopy. One document for diabetes, weight management and heart failure | Use around a procedure should be a shared decision among the patient and the procedural, anesthesia and prescribing teams. Most people can continue the medicine, and the ASA release on the guidance says most patients should continue before elective surgery. Risk is higher during dose increases, at higher doses, with weekly forms and with stomach symptoms. For people judged at higher risk it lists a liquid diet for 24 hours before, a changed anesthesia plan such as rapid-sequence induction, and a stomach ultrasound right before the procedure. Holding is described as an option if the team finds the risk unacceptable, and the length of a hold is called unknown. The authors call the document guidance, not an evidence-based guideline. |
| UK multidisciplinary consensus from eight UK bodies, published January 2025 | Adults having elective surgery. Covers GLP-1 medicines, tirzepatide and SGLT2 inhibitors | Says patients should continue GLP-1 medicines throughout the peri-operative period. The aspiration risk should be discussed using shared decision-making and standard fasting guidance followed. Symptoms alone should not be used to judge what is in the stomach. Regional anesthesia should be considered as the first choice where it suits, and a stomach ultrasound before induction should be considered. The text notes there are no data on the safety or benefit of longer fasting, and that even a week off the medicine is linked with a high risk of leftover contents. |
| UK medicines regulator (MHRA) Drug Safety Update, January 28, 2025 | UK prescribers and patients. Names dulaglutide, exenatide, liraglutide, lixisenatide, semaglutide and tirzepatide | Cites the UK consensus. Asks anesthetists to include aspiration risk in their assessment and to ask about medicines bought privately for weight loss. It sets no pause time and no new fasting rules, and says the evidence was too limited to recommend a specific pause. Its advice to patients is to take their medicine as usual and not stop without first talking to a doctor. |
| Australian and New Zealand recommendations from four bodies, April 2025 | Practitioners giving moderate to deep sedation or anesthesia for surgery and endoscopy | Says elective cessation before a procedure is not recommended, and that leaving out a long-acting dose for one to two weeks is unlikely to change stomach emptying. For daily liraglutide it says to continue, though withholding for three to four days may be considered, without proven added safety. It recommends a 24-hour clear liquid diet followed by standard fasting. Symptoms are not a reliable guide. If these steps are not followed, the patient is treated as non-fasted, with mitigation or deferral. |
| Korean Society of Anesthesiologists consensus, published July 2026 | Patients having anesthesia, including those on GLP-1 based therapy | The authors summarize it as continuing these medicines in most patients with an individual risk assessment, considering a 24-hour clear liquid diet, and using a stomach ultrasound when delayed emptying is suspected. They say the evidence is too thin for a formally graded guideline. |
The multisociety guidance was issued by the ASA, AGA, American Society for Metabolic and Bariatric Surgery, International Society of Perioperative Care of Patients with Obesity and Society of American Gastrointestinal and Endoscopic Surgeons. The UK consensus came from the Association of Anaesthetists, Association of British Clinical Diabetologists, British Obesity and Metabolic Surgery Society, Centre for Perioperative Care, Joint British Diabetes Societies for Inpatient Care, Royal College of Anaesthetists, Society for Obesity and Bariatric Anaesthesia and UK Clinical Pharmacy Association. The Australian and New Zealand recommendations came from the Australian Diabetes Society, National Association of Clinical Obesity Services, Gastroenterological Society of Australia and Australian and New Zealand College of Anaesthetists. Dates are publication or posting dates as the Atlas found them. The Atlas read the multisociety guidance in its journal text. The ASA, AGA and Australian and New Zealand rows come from the bodies' web pages and summaries as the Atlas read them, and the AGA update's advice statements are behind a paywall, so that row follows the AGA's own web summary. The Korean row comes from the published abstract. The ASA page does not call its 2023 guidance withdrawn. It says the ASA later affirmed the value of the more recent multisociety document. The Atlas did not find a separate statement from the metabolic surgery societies or a European anesthesia society.
Where the statements split
A 2024 review read the statements of 14 anesthesia, endocrine and gastroenterology societies and found considerable variation on whether to withhold, for how long, on fasting and on rapid-sequence induction. Its authors tied the variation to a lack of high-quality data. The newer statements narrowed some of those gaps and left others open.
| Topic | ASA 2023 | Multisociety 2024 | UK consensus 2025 | Australia and New Zealand 2025 |
|---|---|---|---|---|
| Holding the medicine before an elective procedure | Consider holding: the day of for daily, a week before for weekly | An option if the team finds the risk unacceptable. Length of a hold unknown. Most can continue | Continue throughout | Elective cessation not recommended |
| Liquid diet beforehand | Follow standard fasting guidance. No evidence for a longer fast | Considered for higher-risk people, 24 hours | Standard fasting. No data on longer fasting | 24-hour clear liquid diet, then standard fasting |
| Stomach ultrasound | Consider it if the clinician is proficient and the medicine was not held | Suggested right before the procedure for the highest-risk people | Should be considered before induction | Can be used at the bedside |
| Anesthesia plan | Full-stomach precautions, or consider delaying or treating as a full stomach if the scan is full or unclear | Adjust the plan, for example rapid-sequence induction | Regional anesthesia first where it suits, plus airway steps | Mitigate or defer if not fasted |
| Stomach symptoms | Consider delaying an elective procedure | Wait until symptoms settle | Symptoms alone should not be used to judge stomach contents | Symptoms are not a reliable indicator |
| Tirzepatide and similar medicines | Written for GLP-1 receptor agonists | Authors say the text may need changes for dual and triple agonists | Named in the statement | Named in the statement |
Cells paraphrase the documents and compress them, so read the source for the full wording. The labels use the same warning text for semaglutide and tirzepatide products.
The one randomized trial: OCULUS
OCULUS, published in JAMA Internal Medicine in 2026, randomized adults who took a GLP-1 or GLP-1/GIP medicine at a stable dose and were having elective upper endoscopy under moderate sedation or monitored anesthesia care. One group held a single dose before the procedure and the other continued as usual. People with planned general anesthesia, chronic opioid use or documented gastroparesis were left out.
The trial measured "clinically significant residual gastric volume": stomach contents that stopped the exam, forced an early stop or a breathing tube, or led to an aspiration event that needed extra monitoring or treatment. It was planned for 120 people and stopped at a preplanned halfway analysis of 60, when the difference crossed its stopping boundary.
| Group | Held one dose | Continued | Difference (90% confidence interval) |
|---|---|---|---|
| Everyone in the interim analysis (60 people) | 3.1% | 25.0% | 21.9 points (7.0 to 36.7) |
| Upper endoscopy alone (35 people) | 5.0% | 46.7% | 41.7 points (17.9 to 65.4) |
| Upper endoscopy plus colonoscopy, clear liquids the day before (25 people) | 0% | 0% | No events in either group |
Source: OCULUS, JAMA Internal Medicine 2026 (NCT06533527). Every case was stomach contents that prevented an adequate exam. No unplanned intubation, aspiration or hospital admission occurred, but the authors say the trial was not powered for rare events and that no observed events should not be read as proof of safety. The liquid-diet finding comes from a subgroup the trial was not powered to test. Upper GI symptoms did not predict who had retained contents, only one dose was held, and glucose control was not evaluated. The confidence intervals are 90%, as the paper reports them.
What the observational studies found
Most other evidence comes from comparing people who used GLP-1 medicines with people who did not, often from hospital or insurance records. These studies cannot show cause, and they disagree with one another.
| Study | Design | Result | Limits |
|---|---|---|---|
| Chang and colleagues, 2024 | Scoping review of 24 studies through March 2024 | Of 8 studies comparing users with non-users, 7 found more leftover stomach contents in users (19% to 56% against 5% to 20%). Three retrospective studies of aspiration events found no significant difference. | Many included studies were case reports or small single-hospital studies. No pooled estimate. |
| Tarar and colleagues, 2025 | Meta-analysis of 12 retrospective endoscopy studies | Retained stomach contents in 14% of users and 2.34% of others (odds ratio 6.30, 95% CI 5.30 to 7.49). Aspiration in 0.73% against 0.35% (odds ratio 1.26, 95% CI 0.86 to 1.87). | Certainty rated very low to low. 95% of users had diabetes against 58% of others. The paper prints two slightly different patient totals. |
| Garza and colleagues, 2024 | Matched case-control at one center, medicine not held | Solid stomach residue at endoscopy in 14% of users against 4% of matched controls. | Retrospective. The Atlas read the abstract only. |
| Barlowe and colleagues, 2024 | US insurance claims, 6.8 million outpatient upper endoscopies in adults 18 to 64 with type 2 diabetes | Lung complications within 14 days were rare, 6 to 25 per 10,000 procedures. Aspiration risk compared with DPP-4 inhibitors: relative risk 0.67 (95% CI 0.25 to 1.75). | Billing codes, crude comparison, people with diabetes under 65 only. |
| Chhabra and colleagues, 2025 | Electronic records (TriNetX), colonoscopy, 126,663 people per group after matching | Aspiration pneumonia: risk ratio 0.70 (95% CI 0.50 to 0.98). | Retrospective record data. |
| Chen and colleagues, 2026 | Electronic records (TriNetX), general anesthesia, 21,948 matched people | Lung complications: hazard ratio 0.682 (95% CI 0.496 to 0.938). Gastrointestinal complications: 1.034 (1.003 to 1.067). | Retrospective record data, published October 2026. |
| Potter and colleagues, 2026 | UK national prospective cohort, 47,039 adults at 119 sites, elective and emergency procedures | Aspiration and/or regurgitation in 1.41% of users (19 of 1,348) and 0.12% of others (57 of 45,691). Odds ratio 11.39 (95% CI 6.47 to 20.05), mostly at the end of anesthesia. | Observational, with aspiration and regurgitation counted together. Management around the procedure varied. |
These studies point in different directions. The UK cohort followed patients forward in time and found a large excess. Several large record-based studies found no excess or a lower risk of lung complications. Outcomes, procedures and designs differ, and none of the studies is a randomized comparison. The Atlas read the Garza, Barlowe, Chhabra, Chen and Potter studies as abstracts.
Colonoscopy and bowel preparation
For colonoscopy the practical question is whether the bowel is clean enough to see. Three meta-analyses of observational studies looked at it and did not agree.
| Analysis | What it pooled | Inadequate bowel prep, users against others | Average bowel prep score (BBPS) difference |
|---|---|---|---|
| Abdulraheem and colleagues, 2026 | 12 observational studies, 123,858 people in all | From 10 of the studies (6,317 users and 14,779 others): 10.86% against 6.39%. Odds ratio 1.55 (95% CI 1.11 to 2.16) | From 5 of the studies: -0.68 (95% CI -0.77 to -0.58) |
| Ahmed and colleagues, 2025 | 6 studies | Odds ratio 1.00 (95% CI 0.73 to 1.37) | From 3 of the 6 studies: -0.36 (95% CI -0.44 to -0.28) |
| Chiu and colleagues, 2025 | 6 studies, 8,778 users and 8,290 others | Risk difference 0.06 (95% CI 0.05 to 0.08) | -0.31 (95% CI -0.39 to -0.23) |
BBPS is the Boston Bowel Preparation Scale, a standard score of how clean the bowel looks, where higher is cleaner. All three analyses agree that scores were slightly lower in users, and they disagree on whether more people had an inadequate prep. None pooled polyp or adenoma detection. The Chiu abstract says two studies found higher detection in users and one found no difference. The Atlas read the Ahmed and Chiu analyses as abstracts. A separate chart review at one hospital, Ghazanfar and colleagues in 2024, compared diets only among people on a GLP-1 medicine and found leftover food at upper endoscopy in 1.5% on a liquid or low-residue diet and 10% on a regular diet. It was retrospective and could not check whether patients followed the diet or took the medicine as prescribed.
Trials still running
ClinicalTrials.gov lists a randomized trial of a 24-hour clear liquid diet before upper endoscopy in people using GLP-1 medicines (NCT06654219, University of Texas Health Science Center at Houston, 136 people planned, recruiting when the Atlas looked). It also lists a randomized trial of a medicine that speeds stomach emptying before elective surgery in people using GLP-1 medicines for weight loss (NCT07100691, Mater Misericordiae University Hospital, 80 people planned). The registry still shows it as not yet recruiting, although its listed start and completion dates have passed. Neither has posted results.
Does the reason for taking it matter?
The labels and most statements treat the medicine the same whether it is used for diabetes or for weight. The multisociety guidance is one document for all uses. It says withholding the medicine only from people who take it for weight management could amount to obesity bias, and that for people with diabetes withholding can raise blood sugar, which has to be weighed against the aspiration risk. The UK and Australian and New Zealand statements raise the same blood sugar point. None of them gives a separate rule for weight management.
Terms you may hear on the day
| Term | What it means |
|---|---|
| Pulmonary aspiration | Stomach contents entering the windpipe and lungs during anesthesia or sedation. |
| Residual or retained gastric contents | Food or liquid still in the stomach after the usual fasting time. |
| Gastric ultrasound | A quick bedside scan that looks at what is in the stomach before sedation. |
| Rapid-sequence induction | A way of starting anesthesia that secures the airway quickly to lower the chance of stomach contents reaching the lungs. |
| Full stomach | An anesthesia term for treating a patient as if the stomach may not be empty. |
| Shared decision-making | The patient and the procedural, anesthesia and prescribing teams decide together after weighing the risks. |
| Dose escalation | The first weeks or months of a GLP-1 medicine, when the dose is stepped up. The multisociety guidance names this stage as higher risk for delayed stomach emptying. |
Quick answers
- Do the Ozempic, Wegovy, Zepbound and Mounjaro labels tell people to stop before surgery?
- In the parts the Atlas read, no. The labels report rare cases of aspiration, say the data cannot show whether changing fasting advice or stopping the medicine would lower the risk, and tell prescribers to have patients mention the medicine before any planned procedure.
- Do the medical societies agree on holding the medicine?
- No. The ASA's 2023 guidance said to consider holding. The October 2024 multisociety guidance says most people can continue and describes holding as an option if the team finds the risk unacceptable. The UK, Australian and New Zealand statements advise against routine cessation before elective procedures, and the Korean statement leans toward continuing. A 2024 review of 14 societies found considerable variation.
- Did the ASA change its advice?
- The ASA issued consensus guidance in June 2023 that suggested considering a hold. In October 2024 it was one of five societies behind new guidance, and its 2023 page now says it affirmed the value of that more recent document. This page reports both and does not rank them.
- Has holding the medicine been tested in a randomized trial?
- For upper endoscopy, yes. OCULUS found less retained stomach content in people who held one dose, but it stopped early at 60 people and excluded planned general anesthesia. The Atlas did not find a randomized trial of holding against continuing before surgery under general anesthesia as of October 2026.
- What about colonoscopy?
- The AGA update and the multisociety guidance cover endoscopy as well as surgery. Studies of bowel preparation disagree on whether more users have an inadequate prep, and the evidence on whether polyp detection changes is thin.
- Is tirzepatide treated differently from semaglutide?
- The Mounjaro and Zepbound labels carry the same warning as Ozempic and Wegovy. The UK and Australian and New Zealand statements name tirzepatide alongside semaglutide, and the multisociety authors say their guidance may need changes for dual and triple agonists.
- Does it matter whether the medicine is for diabetes or for weight?
- The statements do not set separate rules by reason. They note that stopping can raise blood sugar in people with diabetes, and the multisociety guidance warns against singling out people who take the medicine for weight.
- What about emergency surgery?
- The 2023 ASA guidance says urgent and emergency cases go ahead and are treated as having a full stomach. The UK statement says its recommendations may be less applicable to emergency surgery and endoscopy.
- Who decides what happens around a procedure?
- The multisociety guidance and the UK consensus both describe it as a shared decision among the patient and the procedural, anesthesia and prescribing teams. The Atlas does not make that decision and cannot know the details of any one person's situation.
Questions to ask
- Who on my team is making the decision about my GLP-1 medicine around this procedure: the surgeon, the anesthesia team, the person who prescribes it, or all three?
- Does the team want to know which medicine I use, my dose, whether I am still increasing the dose and when I last took it?
- Is the plan going to include a diet change the day before, a stomach ultrasound or a change in how anesthesia is given?
- If I use the medicine for diabetes, who will manage my blood sugar around the procedure?
- Is my procedure planned or urgent, and does that change what the team does?
- Who do I contact, and when, if I have nausea, vomiting or belly pain close to the procedure date?
What is still unknown
- No randomized trial of holding against continuing before surgery under general anesthesia was found. OCULUS covers upper endoscopy and excluded planned general anesthesia.
- How many doses, if any, would need to be held to change stomach contents, and whether that differs by drug, dose or weekly versus daily forms, has not been tested.
- How often aspiration happens, and whether it differs by procedure, is unclear. The studies use different outcomes and point in different directions.
- Whether the 24-hour liquid diet works comes from one trial subgroup and from observational comparisons. Two registered trials may add data.
- Whether poorer bowel preparation changes polyp detection or the need for repeat colonoscopy is not settled.
- The Atlas did not read the patient-counseling sections of the Wegovy and Zepbound labels, the paywalled text of the AGA update or the full ASA, AGA and ANZCA documents.
Sources
- Ozempic (semaglutide) injection: prescribing information Novo Nordisk, on DailyMed (U.S. National Library of Medicine). Label version 5/2026. Official FDA label on DailyMed
- Wegovy (semaglutide) injection and tablets: prescribing information Novo Nordisk, on DailyMed (U.S. National Library of Medicine). Label version 6/2026. One label covers both the injection and the tablets. Official FDA label on DailyMed
- Zepbound (tirzepatide) injection: prescribing information Eli Lilly and Company, on DailyMed (U.S. National Library of Medicine). Label version 8/2026. Official FDA label on DailyMed
- Mounjaro (tirzepatide) injection: prescribing information Eli Lilly and Company, on DailyMed (U.S. National Library of Medicine). Label version 8/2026. Official FDA label on DailyMed
- American Society of Anesthesiologists consensus-based guidance on preoperative management of patients on GLP-1 receptor agonists American Society of Anesthesiologists news release, June 29, 2023. The ASA page says the society later affirmed the value of the more recent October 2024 multisociety guidance. Professional society statement
- AGA rapid clinical practice update on the management of patients taking GLP-1 receptor agonists prior to endoscopy: communication Hashash JG, Thompson CC, Wang AY. Clin Gastroenterol Hepatol. 2024;22(4):705-707. Published online November 2023. PMID 37944573. Journal article
- AGA guidance on GLP-1 receptor agonists before endoscopy American Gastroenterological Association rapid clinical practice update, published in Clinical Gastroenterology and Hepatology in 2024, as summarized on gastro.org. Professional society statement
- Multisociety clinical practice guidance for the safe use of glucagon-like peptide-1 receptor agonists in the perioperative period Kindel TL, et al. Surg Obes Relat Dis. 2024;20(12):1183-1186. From the American Society of Anesthesiologists, American Gastroenterological Association, American Society for Metabolic and Bariatric Surgery, International Society of Perioperative Care of Patients with Obesity and Society of American Gastrointestinal and Endoscopic Surgeons. Published October 29, 2024. PMID 39482213. Journal article
- New multi-society clinical practice guidance released (GLP-1 receptor agonists before elective surgery) American Society of Anesthesiologists news release, October 29, 2024. Professional society statement
- Elective peri-operative management of adults taking glucagon-like peptide-1 receptor agonists, glucose-dependent insulinotropic peptide agonists and sodium-glucose cotransporter-2 inhibitors: a multidisciplinary consensus statement El-Boghdadly K, et al. Anaesthesia. 2025;80(4):412-424. Consensus statement from the Association of Anaesthetists, Association of British Clinical Diabetologists, British Obesity and Metabolic Surgery Society, Centre for Perioperative Care, Joint British Diabetes Societies for Inpatient Care, Royal College of Anaesthetists, Society for Obesity and Bariatric Anaesthesia and UK Clinical Pharmacy Association. PMID 39781571. Journal article
- GLP-1 and dual GIP/GLP-1 receptor agonists: potential risk of pulmonary aspiration during general anaesthesia or deep sedation Medicines and Healthcare products Regulatory Agency (UK), Drug Safety Update, January 28, 2025. Regulator
- Clinical practice recommendations regarding patients taking GLP-1 receptor agonists and dual GLP-1/GIP receptor co-agonists prior to anaesthesia or sedation for surgical and endoscopic procedures Australian Diabetes Society, National Association of Clinical Obesity Services, Gastroenterological Society of Australia and Australian and New Zealand College of Anaesthetists. Dated April 2025. Professional society statement
- Korean consensus-based recommendations for preanesthetic gastric ultrasound and anesthetic considerations for GLP-1 receptor agonist-based therapy Bang YJ, et al., Clinical Practice Guideline Committee of the Korean Society of Anesthesiologists. Korean J Anesthesiol. 2026;79(5):466-487. PMID 42529794. Journal article
- Comparison of societal guidance on perioperative management of glucagon-like peptide-1 receptor agonists: implications for clinical practice and future investigations Chang MG, Bittner EA. Can J Anaesth. 2024;71(9):1302-1315. PMID 39187641. Journal article
- Holding vs continuing GLP-1/GIP agonists before upper endoscopy: the OCULUS randomized clinical trial Ahmad AI, et al. JAMA Intern Med. 2026;186(5):578-584. ClinicalTrials.gov NCT06533527. PMID 41837981. Journal article
- A scoping review of GLP-1 receptor agonists: are they associated with increased gastric contents, regurgitation, and aspiration events? Chang MG, et al. J Clin Med. 2024;13(21):6336. PMID 39518474. Journal article
- Evidence report on the safety of gastrointestinal endoscopy in patients on glucagon-like peptide-1 receptor agonists: a systematic review and meta-analysis Tarar ZI, et al. Diagnostics (Basel). 2025;15(6):770. PMID 40150111. Journal article
- Glucagon-like peptide-1 receptor agonists increase solid gastric residue rates on upper endoscopy especially in patients with complicated diabetes: a case-control study Garza K, et al. Am J Gastroenterol. 2024;119(6):1081-1088. PMID 38534127. Journal article
- Glucagon-like peptide-1 receptor agonists do not increase aspiration during upper endoscopy in patients with diabetes Barlowe TS, et al. Clin Gastroenterol Hepatol. 2024;23(5):739-747. PMID 38759826. Journal article
- Unmasking aspiration risks: a propensity-matched odyssey of GLP-1 receptor agonists and colonoscopy Chhabra P, et al. J Gastroenterol Hepatol. 2025;40(11):2732-2737. PMID 40954421. Journal article
- The impact of glucagon-like peptide-1 receptor agonists on post-anesthetic pulmonary and gastrointestinal adverse events: a target trial emulation using multinational database Chen SS, et al. Am J Med. 2026 (published online October 21, 2026). PMID 42906844. Journal article
- Peri-operative glucagon-like peptide-1 receptor agonist use and outcomes: a national prospective multicentre cohort study Potter TE, et al. Anaesthesia. 2026 (published online September 16, 2026). PMID 42748560. Journal article
- Impact of glucagon-like peptide-1 receptor agonists on colonoscopy outcomes: a systematic review and meta-analysis Abdulraheem A, et al. Clin Endosc. 2026;59(2):211-222. PMID 41943648. Journal article
- Bowel preparation quality in patients using glucagon-like peptide-1 agonists: a systematic review and meta-analysis Ahmed Z, et al. Gastrointest Endosc. 2025;103(2):235-240.e5. PMID 40846241. Journal article
- The impact of glucagon-like peptide-1 receptor agonists on the quality indicators of colonoscopy: a systematic review and meta-analysis Chiu YT, et al. Dig Liver Dis. 2025;57(7):1386-1392. PMID 40121157. Journal article
- Is it necessary to stop glucagon-like peptide-1 receptor agonists prior to endoscopic procedure? A retrospective study Ghazanfar H, et al. World J Gastroenterol. 2024;30(26):3221-3228. PMID 39086638. Journal article
- Protective benefits of a clear liquid diet on residual gastric content in patients taking a GLP-1 receptor agonist prior to anesthesia (NCT06654219) ClinicalTrials.gov record NCT06654219. Sponsor: The University of Texas Health Science Center, Houston. Status when the Atlas looked: recruiting, no posted results. Trial registry
- Preoperative metoclopramide to enhance gastric emptying in patients on GLP-1 receptor agonists for weight loss (NCT07100691) ClinicalTrials.gov record NCT07100691. Sponsor: Mater Misericordiae University Hospital. Status when the Atlas looked: not yet recruiting, no posted results. Trial registry