DOI: 10.1097/brs.0000000000005773 ISSN: 0362-2436

Long-Term Mechanical Complications After Lumbar Fusion in Patients Receiving Tirzepatide vs Other GLP-1 Receptor Agonists

Ryan Wang, Humaira Islam, Arjuna Karikaran, William Zeng, Alexander T. Hong, Hannah Cho, Syed I. Khalid, Ankit I. Mehta

Study Design.

Retrospective cohort study

Objective.

To compare short-term outcomes and long-term mechanical complications following lumbar fusion in patients receiving tirzepatide versus non-tirzepatide glucagon-like peptide-1 receptor agonists (GLP-1 RAs).

Summary of Background Data.

GLP-1 RAs have demonstrated metabolic and anti-inflammatory effects that may influence postoperative recovery. Tirzepatide, a dual GLP-1/ glucose-dependent insulinotropic polypeptide (GIP), has shown greater metabolic efficacy than traditional GLP-1 RAs, though its impact on spinal fusion outcomes remains unclear.

Methods.

A retrospective cohort analysis was performed using the TriNetX Global Collaborative Network for adult patients undergoing lumbar fusion. Exposure was defined by tirzepatide or non tirzepatide GLP-1 RAs prescription within one year before surgery. Propensity score matching (1:1) was conducted using demographic and clinical covariates. Ninety-day complications and mechanical outcomes from 1-3 years were evaluated using risk ratios (RRs) with 95% confidence intervals (CIs).

Results.

After matching, ninety-day medical complications, hospitalizations and emergency department visits were similar between groups ( P >0.05). At one year, pseudoarthrosis (3.0% vs 3.8%), instrumentation failure (1.4% vs 1.7%), and revision surgery (1.3% vs 1.3%) were comparable between groups ( P >0.05). By two years, tirzepatide was associated with significantly lower pseudoarthrosis (3.1% vs 5.5%, RR 0.56, 95% CI 0.35–0.90, P =0.016) and instrumentation failure (1.5% vs 3.5%, RR 0.42, 95% CI 0.22–0.80, P =0.006), with similar revision rates. At three years, pseudoarthrosis (3.1% vs 6.0%, RR 0.51, 95% CI 0.32–0.82, P =0.005) and instrumentation failure (1.6% vs 3.7%, RR 0.43, 95% CI 0.23–0.79, P =0.005) remained significantly lower, while revision surgery remained nonsignificant.

Conclusion.

Tirzepatide was associated with comparable short-term safety and lower rates of long-term mechanical complications after lumbar fusion. These findings suggest differences in mechanical outcomes that emerge over extended follow-up and warrant prospective comparative evaluation.

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