← Issue №1/ week of Jun 24, 2026/Esophagus/Reflux

Incidence of Gastrointestinal Adverse Events and Healthcare Resource Utilization in Patients Using Glucagon-Like Peptide-1 Analogs: A Real-World Study.

From GI Signals issue №1: what this paper found, what it changes, and where it sits against the current standard of care, reviewed by Simon Mathews, MD.

Esophagus/Reflux retrospective · n=164,987 · Jul 8, 2026 · Dig Dis Sci · IF 2.5

Incidence of Gastrointestinal Adverse Events and Healthcare Resource Utilization in Patients Using Glucagon-Like Peptide-1 Analogs: A Real-World Study.

New evidenceepidemiologyGERDgastroparesisacute pancreatitis
Clinical takeawayCounsel patients with DM or obesity starting GLP-1 analogs about the high likelihood (1 in 3) of GI side effects, particularly nausea, vomiting, and GERD, and monitor for gastroparesis symptoms (early satiety, bloating). Note the reduced bowel obstruction risk and no significant increase in ER visits or hospitalizations despite higher EGD use.
What it foundGLP-1 therapy was associated with a 31.9% rate of GI adverse events at one year (NNH 17.2), including nausea/vomiting (HR 1.24), GERD (HR 1.18), and gastroparesis (HR 1.57), while reducing bowel obstruction risk (HR 0.86).
ContextConfirms and quantifies real-world GI risks of GLP-1 analogs beyond clinical trial data, while challenging assumptions about healthcare utilization (lower admissions despite more EGDs). Prior evidence focused on GLP-1 benefits with less emphasis on AEs.
Emergingsuggested applicable standard· American College of Gastroenterology (ACG), ACG Clinical Guideline for the Diagnosis and Management of Gastroesophageal Reflux Disease (Katz PO, Dunbar KB, Schnoll-Sussman FH, Greer KB, Yadlapati R, Spechler SJ), Am J Gastroenterol 2022;117(1):27-56

No single passage of this standard matched the paper closely enough to quote, so none is shown. The standard is cited above.

Our full summary of this standard

In patients with classic GERD symptoms (heartburn, regurgitation) and no alarm symptoms, give an 8-week trial of empiric PPI ONCE DAILY before a meal (strong, moderate evidence); administer PPI 30-60 minutes before a meal rather than at bedtime (strong, moderate). Endoscopy is the FIRST test in patients presenting with dysphagia or other alarm symptoms, the guideline names weight loss and GI bleeding, and also in patients with multiple risk factors for Barrett's esophagus (strong, low). If classic symptoms respond to the 8-week trial, attempt to discontinue the PPI (conditional, low); for patients without erosive esophagitis or Barrett's whose symptoms resolved, an attempt at discontinuation should be made; patients requiring maintenance should take the lowest effective dose. If symptoms do not respond adequately to the 8-week trial, or return on discontinuation, perform diagnostic endoscopy, ideally after PPIs are stopped for 2-4 weeks (strong, low). Where GERD is suspected but unclear and endoscopy shows no objective evidence, perform reflux monitoring OFF therapy to establish the diagnosis (strong, low); conversely, do NOT perform off-therapy reflux monitoring solely as a diagnostic test in patients already known to have LA grade C or D esophagitis or long-segment Barrett's, because the diagnosis is already established (strong, low). In refractory GERD, optimize PPI therapy first (strong, moderate); then pH monitoring OFF PPIs if GERD was not previously established by pH study, long-segment Barrett's, or LA grade C/D esophagitis, versus impedance-pH ON PPIs where GERD is already established but symptoms persist on twice-daily PPI (both conditional, low). Before antireflux surgery or endoscopic therapy, HRM is recommended to rule out achalasia and absent contractility, with provocative testing (e.g., multiple rapid swallows) to identify contractile reserve in ineffective esophageal motility; on-therapy reflux monitoring is suggested before intervention in patients with prior objective GERD findings who remain symptomatic. Antireflux surgery by an experienced surgeon is an option for patients with OBJECTIVE evidence of GERD, with severe esophagitis (LA C/D), large hiatal hernia, or persistent troublesome symptoms benefiting most; TIF is suggested only for troublesome regurgitation or heartburn in patients who do not wish to undergo antireflux surgery and who are WITHOUT severe esophagitis (LA C/D) or hiatal hernia >2 cm. For extraesophageal symptoms WITHOUT typical GERD symptoms, perform reflux testing BEFORE starting PPI therapy (strong, moderate); with concomitant typical symptoms, consider twice-daily PPI for 8-12 weeks before further testing (conditional, low). Lifestyle: weight loss in overweight/obese patients (strong, moderate); avoid meals within 2-3 hours of bedtime, avoid tobacco, avoid trigger foods, and elevate the head of the bed for nighttime symptoms (all conditional, low).

American College of Gastroenterology (ACG), ACG Clinical Guideline for the Diagnosis and Management of Gastroesophageal Reflux Disease (Katz PO, Dunbar KB, Schnoll-Sussman FH, Greer KB, Yadlapati R, Spechler SJ), Am J Gastroenterol 2022;117(1):27-56 · reviewed 2026-07-23 ↗
Nathani P … Sharma P · Digestive Diseases and Sciences · IF 2.5 · PubMed ↗Permalink
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