Reduced Complications and Improved Survival With Postoperative GLP-1 Receptor Agonist Use Following Lumbar Arthrodesis

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Authors: Emma B. Proffitt, Samuel W. Rice, Ryan M. Schiedo, Michael P. Stauff
Cited by: 1
References: 29

Abstract

Study Design Retrospective propensity-score-matched cohort study. Objectives To evaluate whether postoperative glucagon-like peptide-1 receptor agonist (GLP-1 RA) use is associated with fewer complications, lower pseudarthrosis, and improved survival after lumbar fusion in adults aged 50 years and older. Methods The TriNetX Global Collaborative Network was queried to identify adults ≥50 years who underwent lumbar arthrodesis (2010-2025). GLP-1 RA exposure was defined as an active prescription within 1 to 90 days postoperatively. The comparison group consisted of patients without a GLP-1 RA prescription during this window. Propensity score matching adjusted for demographics, BMI, hemoglobin A1c, preoperative GLP-1 RA use, and comorbidities. Outcomes: 90-day and 1-year infectious, pulmonary, and thromboembolic complications, 1-year pseudarthrosis, and 1-year mortality rates. Survival was assessed with Kaplan Meier and Cox regression. Results Among 169 286 patients who underwent lumbar arthrodesis, 1844 had postoperative GLP-1 RA use and 167 442 did not. After matching, 1816 patients remained in each cohort. Postoperative GLP-1 RA use was associated with lower 90-day pneumonia (Risk Ratio [RR] 0.51), surgical site infection (RR 0.58), sepsis (RR 0.64), urinary tract infection (RR 0.56), wound dehiscence (RR 0.46), and venous thromboembolism (RR 0.54) (all P < 0.05), and 1-year lower hazard of death (HR 0.38; P = 0.018). Conclusion In this large propensity-score-matched cohort, postoperative GLP-1 RA use was associated with fewer early infectious, pulmonary, wound, and thromboembolic complications and improved 1-year survival after lumbar spinal fusion.

Fields of Study & Subjects

Anesthesia and Pain Management Spine and Intervertebral Disc Pathology Diabetes Treatment and Management

Publication details

Journal / source
Global Spine Journal
Publisher
SAGE Publications
Volume
16
Issue
7
Pages
21925682261442187–21925682261442187
Publication date
13 April 2026
Language
EN