BACKGROUND Glucagon-like peptide-1 (GLP) receptor agonists have demonstrated anti-inflammatory and wound-healing properties, but their impact on outcomes after dermatologic surgery has not been evaluated. OBJECTIVE This study assessed the one-month risk of postoperative inflammatory complications (IC) in patients taking GLPs. METHODS Patients undergoing Mohs Micrographic Surgery and wide local excisions for melanoma or nonmelanoma skin cancer while taking a GLP were identified using the TriNetx Research Network. GLPs included semaglutide, tirzepatide, liraglutide, dulaglutide, exenatide, albiglutide, and lixisenatide. IC included wound disruption, hematoma, infection of the skin and subcutaneous tissue, infections after a procedure, and other complications of procedures. After accounting for demographics and proinflammatory comorbid conditions, hazard ratios and 95% confidence intervals were used to identify the one-month risk of postoperative complications. RESULTS Compared with patients without GLP use, the GLP cohort was associated with a significantly reduced risk of infection after a procedure, wound disruption, skin and subcutaneous tissue infection, hematoma, and other complications. Among individual drug comparisons, semaglutide and tirzepatide demonstrated the greatest reductions in postoperative complications. CONCLUSION GLP receptor agonists were associated with a significantly reduced risk of postoperative inflammatory complications after dermatologic surgery, supporting their perioperative safety and potential beneficial role in wound healing.
Vu et al. (Mon,) studied this question.