Key result
Preoperative GLP-1RA use is linked to ~75% lower 90-day DVT risk after unicompartmental knee arthroplasty.
Why the study?
Does preoperative GLP-1 receptor agonist use reduce postoperative complications in adult patients undergoing primary unicompartmental knee arthroplasty?
Cohort (n=2,276)
Yes
Does preoperative GLP-1 receptor agonist use reduce postoperative complications in adult patients undergoing primary unicompartmental knee arthroplasty?
Effect estimate: RRR 75% (95% CI 15-93)
Absolute Event Rate: 0.4% vs 1.4%
p-value: p=0.013
Preoperative GLP-1 receptor agonist use is associated with significantly lower rates of thromboembolic, infectious, and wound-related complications following unicompartmental knee arthroplasty.
Preoperative GLP-1 use was associated with fewer UKA complications; hypothesis-generating and should not yet change practice.
Background Glucagon-like peptide-1 (GLP-1) receptor agonists have demonstrated benefits in diabetes and obesity management, but their impact on outcomes following unicompartmental knee arthroplasty (UKA) remains unexplored. This study evaluates the influence of preoperative GLP-1 agonist use on postoperative complications following UKA. Methods A national claims database was queried to identify patients undergoing primary UKA between 2010 and 2021. Patients with preoperative GLP-1 prescriptions were 1:1 propensity-matched to non-users based on age, sex, Charlson Comorbidity Index, diabetes, obesity, and tobacco use, yielding two balanced cohorts of 1,138 patients each (mean age 61.1 years, 53% female). Successful matching was confirmed with standardized mean differences <0.001 for all variables. Primary outcomes included 90-day and 2-year complications. Categorical variables were compared using chi-square tests with relative risk reduction (RRR) and 95% confidence intervals. Results At 90 days, GLP-1 users demonstrated significantly lower rates of deep vein thrombosis (0.4% vs. 1.4%; RRR = 75%; 95% CI: 15-93%; P = 0.013), wound complications (0.0% vs. 1.2%; RRR = 100%; P < 0.001), and surgical site infections (0.1% vs. 1.2%; RRR = 93%; 95% CI: 34-99%; P = 0.002) compared to non-users. No significant differences were observed in pulmonary embolism, acute kidney injury, urinary tract infection, hematoma, transfusion requirements, or readmissions. At 2 years, GLP-1 users had significantly lower rates of prosthetic joint infection (0.4% vs. 1.4%; RRR = 75%; 95% CI: 15-93%; P = 0.013). All-cause revision rates showed a favorable trend in GLP-1 users but did not reach statistical significance (2.3% vs. 3.6%; RRR = 37%; P = 0.083). Conclusion Preoperative GLP-1 receptor agonist use was associated with lower rates of thromboembolic, infectious, and wound-related complications following UKA without an observed increase in other adverse events. These findings may reflect both medication-related effects and broader improvements in metabolic optimization. Prospective studies with detailed metabolic data are needed to further evaluate these associations.
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Fuller et al. (2026) conducted a cohort in Unicompartmental knee arthroplasty (n=2,276). Preoperative GLP-1 receptor agonist vs. Non-users was evaluated on 90-day deep vein thrombosis (RRR 75%, 95% CI 15-93, p=0.013). Preoperative GLP-1 receptor agonist use was associated with a 75% relative risk reduction in 90-day deep vein thrombosis and lower rates of infectious and wound-related complications following unicompartmental knee arthroplasty.
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