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· DOS Abstracts

Bone, Subcutaneous Tissue and Plasma

Pharmacokinetics of Vancomycin in Total Knee

Replacement Patients

Mats Bue, Mikkel Tøttrup, Pelle Hanberg, Otto Langhoff, Hanne Birke-Sørensen,

Kjeld Søballe

Department of Orthopaedic Surgery, Horsens Regional Hospital; Department

of Orthopaedic Surgery, Randers Regional Hospital; Orthopaedic Research

Unit, Aarhus University Hospital; Department of Orthopaedic Surgery, Horsens

Regional Hospital; Orthopaedic Research Unit, Aarhus University Hospital;

Department of Orthopaedic Surgery, Aarhus University Hospital

Background:

High treatment failure rates and the need for prolonged anti-

microbial therapy for osteomyelitis and implant-associated infections suggest

that antimicrobial bone penetration may be incomplete. Assessment of the bone

pharmacokinetics of antimicrobials is challenged by a lack of validated methods.

Purpose / Aim of Study:

The objective of this study was to compare and de-

scribe plasma, subcutaneous tissue and bone pharmacokinetics of vancomycin

in patients.

Materials and Methods:

Postoperatively, 1,000 mg of vancomycin was ad-

ministered to ten male patients undergoing total knee replacement as a single

dose over 100 min. Plasma, subcutaneous tissue and bone pharmacokinetics

were investigated over 8 hours. Microdialysis catheters were applied for collec-

tion of samples in bone and subcutaneous tissue. Venous samples were drawn

from a venous catheter. The vancomycin concentration in microdialysates was

determined using ultra-high performance liquid chromatography, whilst the free

plasma concentration was determined using Cobas c501.

Findings / Results:

For all extravascular tissue, an impaired penetration was

demonstrated. Area under the concentration- time curve (AUC) were found

lower for bone and subcutaneous tissue when compared to free plasma. The

lowest AUC was found in cortical bone.

Conclusions:

Bone penetration of vancomycin was found to be incomplete and

delayed. Future studies should further focus on validating the applicability of

microdialysis for assessment of antimicrobial bone pharmacokinetics.

No conflicts of interest reported

49.