[Translated article] Complications of intraosseous administration of vancomycin in total hip arthroplasty

W F Martínez1, L Camacho Terceros2, F Garbini2

  • 1Facultad de Medicina, Pontificia Universidad Católica Argentina, Buenos Aires, Argentina; Clínica Privada Hispano Argentina, Buenos Aires, Argentina; Grupo GRECARO, Ciudad Autónoma de Buenos Aires, Argentina.

Abstract

Insights

Intraosseous vancomycin in total hip arthroplasty (THA) is safe for patients at risk of methicillin-resistant Staphylococcus aureus (MRSA) colonization, showing a 0% periprosthetic joint infection (PJI) rate and fewer logistical issues.

Area of Science:

  • Orthopedic Surgery
  • Infectious Disease Prevention
  • Pharmacology

Background:

  • Intravenous antibiotic prophylaxis has reduced periprosthetic joint infection (PJI) rates in hip surgeries.
  • Vancomycin is crucial for patients colonized with methicillin-resistant Staphylococcus aureus (MRSA) or at high risk.
  • Intraosseous vancomycin delivery may improve efficacy in total hip arthroplasty (THA).

Purpose of the Study:

  • To evaluate the safety and efficacy of intraosseous vancomycin administration in primary THA patients at risk for MRSA colonization.
  • To assess the incidence of complications and PJI following intraosseous vancomycin prophylaxis.

Main Methods:

  • Retrospective case series of 53 patients undergoing primary THA between March and December 2023.
  • Patients received 500mg of intraosseous vancomycin into the greater trochanter, alongside standard IV prophylaxis.
  • Complications and PJI rates were monitored during hospitalization and for three months post-surgery.

Main Results:

  • A total of 500mg intraosseous vancomycin was administered per patient.
  • The overall complication incidence was 1.64%.
  • No cases of PJI were reported at the 90-day follow-up.

Conclusions:

  • Intraosseous vancomycin, combined with standard IV prophylaxis, is a safe adjunctive treatment for THA patients at risk of MRSA colonization.
  • This method demonstrated no significant adverse effects and achieved a 0% PJI rate at 90 days.
  • Intraosseous delivery simplifies vancomycin administration logistics.