Abstract
Background
Prophylactic antibiotics reduce the risk of deep infection after primary TKA. However, conventional systemic dosing may not provide adequate tissue concentrations against more resistant organisms such as coagulase-negative staphylococci. Regional intravenous administration of antibiotics after tourniquet inflation achieves far higher tissue concentrations but requires foot vein cannulation. The intraosseous route may offer a rapid and reliable method of regional administration.
Questions/Purposes
We compared tissue concentrations of cefazolin achieved with systemic versus regional intraosseous administration.
Methods
Twenty-two patients undergoing primary TKA were randomized into two groups. Group 1 received 1 g cefazolin systemically 10 minutes before tourniquet inflation. Group 2 received 1 g cefazolin intraosseously in 200 mL of normal saline through a tibial cannula after tourniquet inflation and before skin incision. Subcutaneous fat and femoral bone samples were taken at set intervals during the procedure and antibiotic concentrations measured using a validated technique involving high-performance liquid chromatography.
Results
The overall mean tissue concentration of cefazolin in subcutaneous fat was 186 ug/g in the intraosseous group and 11 ug/g in the systemic group. The mean tissue concentration in bone was 130 ug/g in the intraosseous group and 11 ug/g in the systemic group. These differences were consistent across all sample time points throughout the procedure.
Conclusions
Intraosseous regional administration can achieve concentrations of antibiotic in tissue an order of magnitude higher than systemic administration. Further work is required to determine if this translates into increased efficacy in preventing infection, particularly against coagulase-negative staphylococci.
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Acknowledgments
We thank Irene Zeng, MSc (Hons), for her assistance with statistical analysis, Grant Moore, BSc (Hons), for his assistance with laboratory analysis, and the charitable trust Clinical Research and effective practice (CCRep) for their funding support. We also thank Vidicare (San Antonio, TX, USA) for supplying the intraosseous needles without charge.
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The institution of one of the authors (MZ) received funding from the Centre for Clinical Research and effective practice (CCRep), a charitable trust with no relationship to the subject of this article.
All ICMJE Conflict of Interest Forms for authors and Clinical Orthopaedics and Related Research editors and board members are on file with the publication and can be viewed on request.
Each author certifies that his or her institution approved the human protocol for this investigation, that all investigations were conducted in conformity with ethical principles of research, and that informed consent for participation in the study was obtained.
Clinical Orthopaedics and Related Research neither advocates nor endorses the use of any treatment, drug, or device. Readers are encouraged to always seek additional information, including FDA-approval status, of any drug or device prior to clinical use.
Procedures and sample collection were performed at Middlemore Hospital, Auckland, New Zealand. Sample analysis was performed at Canterbury Health Laboratories, Christchurch, New Zealand.
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Young, S.W., Zhang, M., Freeman, J.T. et al. Higher Cefazolin Concentrations with Intraosseous Regional Prophylaxis in TKA. Clin Orthop Relat Res 471, 244–249 (2013). https://doi.org/10.1007/s11999-012-2469-2
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DOI: https://doi.org/10.1007/s11999-012-2469-2