Quantified Metrics of Gastric Emptying Delay by Glucagon-Like Peptide-1 Agonists: A Systematic Review and Meta-Analysis With Insights for Periprocedural Management

Author:

Hiramoto Brent12ORCID,McCarty Thomas R.345ORCID,Lodhia Nayna A.12,Jenkins Andrew12,Elnaiem Ahmed26ORCID,Muftah Mayssan12ORCID,Flanagan Ryan12,Chan Walter W.12ORCID

Affiliation:

1. Center for Gastrointestinal Motility, Division of Gastroenterology, Hepatology and Endoscopy, Brigham and Women's Hospital, Boston, Massachusetts, USA;

2. Harvard Medical School, Boston, Massachusetts, USA;

3. Underwood Center for Digestive Disorders, Houston Methodist Hospital, Houston, Texas, USA;

4. Weill Cornell Medical College, New York, New York, USA;

5. Texas A&M University, School of Medicine, Bryan College Station, Texas, USA;

6. Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Abstract

INTRODUCTION: Divergent recommendations for periprocedural management of glucagon-like peptide-1 (GLP-1) receptor agonist (GLP-1 RA) medications rely on limited evidence. We performed a systematic review and meta-analysis to provide quantitative measures of gastric emptying relevant to mechanisms of weight loss and to periprocedural management of GLP-1 RA. We hypothesized that the magnitude of gastric emptying delay would be low and of limited clinical significance to procedural sedation risks. METHODS: A protocolized search identified studies on GLP-1 RA that quantified gastric emptying measures. Pooled estimates using random effects were presented as a weighted mean difference with 95% confidence intervals (CIs). Univariate meta-regression was performed to assess the influence of GLP-1 RA type, short-acting vs long-acting mechanism of action, and duration of treatment on gastric emptying. RESULTS: Fifteen studies met the inclusion criteria. Five studies (n = 247) utilized gastric emptying scintigraphy. Mean T1/2 was 138.4 minutes (95% CI 74.5–202.3) for GLP-1 RA vs 95.0 minutes (95% CI 54.9–135.0) for placebo, with a pooled mean difference of 36.0 minutes (95% CI 17.0–55.0, P < 0.01, I 2 = 79.4%). Ten studies (n = 411) utilized the acetaminophen absorption test, with no significant delay in gastric emptying measured by Tmax, area under the curve (AUC)4hr, and AUC5hr with GLP-1 RA (P > 0.05). On meta-regression, the type of GLP-1 RA, mechanism of action, and treatment duration did not impact gastric emptying (P > 0.05). DISCUSSION: While a gastric emptying delay of ∼36 minutes is quantifiable on GLP-1 RA medications, it is of limited magnitude relative to standard periprocedural fasting periods. There were no substantial differences in gastric emptying on modalities reflective of liquid emptying (acetaminophen absorption test), particularly at time points relevant to periprocedural care.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Ovid Technologies (Wolters Kluwer Health)

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