The bactericidal effect of vancomycin is not altered by tranexamic acid, adrenalin, dexamethasone, or lidocaine in

Christiane Schwerdt1, Eric Röhner1, Sabrina Böhle1

  • 1Orthopaedic Professorship of the University Hospital Jena, Campus Eisenberg, Klosterlausnitzer Str. 81, 07607, Eisenberg, Germany.

Scientific Reports
|May 25, 2021
PubMed

Insights

Intrawound vancomycin powder is effective against periprosthetic joint infections after knee replacement. Combining vancomycin with tranexamic acid, adrenalin, lidocaine, or dexamethasone does not alter its bactericidal effect in vitro.

Area of Science:

  • Orthopedic Surgery
  • Infectious Diseases
  • Pharmacology

Background:

  • Periprosthetic joint infection (PJI) is a serious complication of total knee arthroplasty (TKA).
  • Intrawound vancomycin powder shows promise for preventing PJI.
  • Other local agents are frequently used in TKA, raising concerns about potential interactions.

Purpose of the Study:

  • To evaluate if tranexamic acid, adrenalin, lidocaine, or dexamethasone inhibit the bactericidal effect of vancomycin.
  • To assess the in vitro efficacy of vancomycin when combined with commonly used local agents in TKA.

Main Methods:

  • Agar diffusion tests were performed using Staphylococcus aureus and Staphylococcus epidermidis.
  • Vancomycin was tested alone, in combination with other agents, and alone with each agent.
  • Zones of inhibition were measured to quantify the bactericidal effect.

Main Results:

  • Vancomycin demonstrated a consistent bactericidal effect against both bacterial strains.
  • No significant alteration in vancomycin's inhibitory zone was observed when combined with tranexamic acid, adrenalin, lidocaine, or dexamethasone.
  • The tested agents alone did not exhibit any bactericidal activity.

Conclusions:

  • Tranexamic acid, adrenalin, lidocaine, and dexamethasone do not inhibit the in vitro bactericidal efficacy of vancomycin against staphylococci.
  • These findings support the concurrent use of vancomycin with these agents in TKA procedures without compromising anti-infective properties.

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