Gynecologic Oncology Reports (Jun 2025)

The effect of intrawound vancomycin powder on surgical site infection in inguinal lymph node dissection: a randomized controlled trial pilot study

  • Jessica B. DiSilvestro,
  • Emily Zitek,
  • Katina Robison,
  • Jasmine Ebott,
  • Corinne Jansen,
  • Katrin Eurich,
  • Cara Mathews,
  • Paul DiSilvestro,
  • Matthew Oliver,
  • Ashley Stuckey,
  • Katherine Miller,
  • Elizabeth Lokich

DOI
https://doi.org/10.1016/j.gore.2025.101765
Journal volume & issue
Vol. 59
p. 101765

Abstract

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Background: Inguinal lymph node dissections are morbid surgeries with high rates of postoperative wound infections. The primary objective of this pilot study was to assess the feasibility of implementing a randomized controlled trial to assess the impact of intrawound vancomycin powder on postoperative complications after inguinal lymph node dissection in patients with vulvar cancer. Secondary objectives included 1) 30-day composite postoperative complication rate, and 2) adverse effects. Methods: This was a single-site, unblinded randomized controlled trial. Patients with vulvar cancer planning to undergo an inguinal lymph node dissection were randomized 1:1 to receive intrawound vancomycin powder at the time of surgery versus standard of care without vancomycin powder. Descriptive statistics and Chi-square were utilized. Results: Between October 2022 to May 2024, 31 patients met eligibility criteria and 30 patients enrolled (97 % recruitment rate). Three patients did not undergo surgery (90 % retention rate). All patients received their correctly assigned arm and all patients completed the postoperative follow-up (100 % adherence rate).One patient in the vancomycin group had a composite postoperative complication (hematoma), while three patients in the control arm had a complication (three inguinal surgical site infections) [8 % vs. 21 %, p = 0.32]. There were no postoperative infections identified in the patients who received intrawound vancomycin powder. No adverse events occurred with the application of vancomycin. Conclusion: This pilot study showed that this was a feasible trial with high recruitment, retention and adherence rates. The data supports proceeding with a larger trial to further elucidate the impact of this low-cost intervention.Trial Registration: ClinicalTrials.gov Identifier: NCT05625373.

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