Evidence map›Paper›PMID 42405290›Full record

ArticleGastro hep advances2026

The Effect of Glucagon-Like Peptide-1 Receptor Agonists on Pain Management in Chronic Pancreatitis: A Real-World Cohort Study.

Arkadeep Dhali, Rick Maity, Fayaz Khan, Abdul Rafae Faisal, Jyotirmoy Biswas, Adnan Bhat, Sushobhon Ghosh

Abstract read
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Article in Gastro hep advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Arkadeep DhaliAcademic Unit of Gastroenterology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Rick MaitySchool of Medical Science and Technology, Indian Institute of Technology Kharagpur, Kharagpur, India.
Fayaz KhanDepartment of Palliative Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, New York.
Abdul Rafae FaisalDepartment of General Medicine, CMH Multan Institute of Medical Sciences, Multan, Pakistan.
Jyotirmoy BiswasDepartment of General Medicine, Barasat Government Medical College and Hospital, Kolkata, India.
Adnan BhatDepartment of Hospital Medicine, University of Florida, Gainesville, Florida.
Sushobhon GhoshDepartment of General Medicine, Dhaka Medical College and Hospital, Dhaka, Bangladesh.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Chronic pancreatitis (CP) is a debilitating inflammatory condition characterized by irreversible glandular destruction and intractable pain. Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) have demonstrated anti-inflammatory properties in preclinical models, yet their impact on clinical outcomes in CP remains unexplored. Methods: In this retrospective cohort study, adult patients (≥18 years) with CP were identified from the TriNetX US Collaborative Network. Patients were stratified into the following two cohorts: those prescribed GLP-1 RAs and a control group without such prescriptions. 1:1 propensity score matching was performed to balance cohorts for age, sex, race, and key comorbidities. Primary outcomes were assessed over a 3-year observation period. Hazard ratios (HRs) were estimated using Kaplan-Meier survival analysis. Results: After matching, 10,625 patients were included in each cohort (mean age 59.6 ± 13.1 years; 53.7% female). GLP-1 RA users had a 41% lower hazard of initiating chronic opioids (HR 0.59, 95% confidence interval [CI] 0.52-0.67; Conclusion: GLP-1 RA use was associated with a substantial reduction in new opioid prescriptions and invasive pancreatic interventions in CP. These findings suggest that GLP-1 RAs may be helpful in symptom control and multidisciplinary management of selected cases.

Indexed as

Abdominal PainAnalgesicChronic PancreatitisGLP-1 Receptor AgonistsOpioid

Identifiers

PMID42405290
PMCPMC13330660

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.