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Serum and Wound Vancomycin Levels After Intrawound Administration in Primary Total Joint Arthroplasty
Jeremiah D Johnson1, Joseph M Nessler2, Ryan D Horazdovsky1
1Department of Orthopaedic Surgery, Regions Hospital, St. Paul, Minnesota; Department of Orthopaedic Surgery, University of Minnesota, Minneapolis, Minnesota.
Background:
Periprosthetic joint infection is the most common cause of readmissions after total joint arthroplasty (TJA). Intrawound vancomycin powder (VP) has reduced infection rates in spine surgery; however, there are no data regarding VP in primary TJA.
Methods:
Thirty-four TJA patients received 2 g of VP intraoperatively to investigate VP's pharmacokinetics. Serum and wound concentrations were measured at multiple intervals over 24 hours after closure.
Results:
All serum concentrations were subtherapeutic (<15μg/mL) and peaked 12 hours after closure (4.7μg/mL; standard deviation [SD], 3.2). Wound concentrations were 922 μg/mL (SD, 523) 3 hours after closure and 207 μg/mL (SD, 317) at 24 hours. VP had a half-life of 7.2 hours (95% confidence interval, 7.0-9.3) in TJA wounds.
Conclusions:
VP produced highly therapeutic intrawound concentrations while yielding low systemic levels in TJA. VP may serve as a safe adjunct in the prevention of periprosthetic joint infection.
Insights
Intrawound vancomycin powder (VP) in total joint arthroplasty (TJA) achieved high wound concentrations and low serum levels. VP may help prevent periprosthetic joint infection after TJA.
Area of Science:
- Orthopedic Surgery
- Infectious Disease
- Pharmacokinetics
Background:
- Periprosthetic joint infection is a leading cause of readmission after total joint arthroplasty (TJA).
- Intrawound vancomycin powder (VP) is effective in reducing infection rates in spinal surgery.
- Limited data exist on VP's efficacy and safety in primary TJA.
Purpose of the Study:
- To investigate the pharmacokinetics of intraoperative VP in patients undergoing primary TJA.
- To determine serum and wound concentrations of VP over 24 hours postoperatively.
- To assess the potential of VP as an adjunct for preventing periprosthetic joint infection.
Main Methods:
- A prospective study involving 34 TJA patients.
- Administration of 2 g of VP intraoperatively.
- Measurement of serum and wound VP concentrations at multiple time points up to 24 hours.
Main Results:
- Serum VP concentrations remained subtherapeutic (<15μg/mL) throughout the study period.
- Peak serum concentration was 4.7μg/mL at 12 hours post-closure.
- Wound VP concentrations were high, measuring 922 μg/mL at 3 hours and 207 μg/mL at 24 hours.
- VP exhibited a half-life of 7.2 hours within TJA wounds.
Conclusions:
- Intraoperative VP in TJA yields therapeutic intrawound concentrations.
- Systemic absorption of VP was minimal, suggesting a favorable safety profile.
- VP may be a valuable adjunct in preventing periprosthetic joint infections in TJA.
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