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Ancef Dosage in Knee Arthroplasty : Tourniquet Clinical Trial

Infections Joint Prosthetic

Tourniquet inflation during total knee arthroplasty (TKA) is commonly used to reduce bleeding in the surgical field; thereby facilitating exposure and cementation. However, reducing circulation to the leg may also reduce antibiotic distribution to the peri-incisional tissues. Once inflated, further parenteral addition of antibiotics is not likely to achieve peak concentration. Some studies propose techniques of regional prophylaxis with a tourniquet to achieve higher cefazolin tissue concentrations. To our knowledge, the effect of tourniquet application on antibiotic tissue concentrations during total knee arthroplasty has not been explored. Furthermore, the effect of time from dose to incision, participants weight, and length of surgery on local tissue concentrations of Ancef are poorly understood. Considering that infections remain the leading source of early reoperation and revision surgery, insight and optimization of local tissue antibiotics is of paramount interest.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 to 85

Participation Criteria

Inclusion Criteria:

* Adults ages 18-85 who require a primary total knee replacement
* Any gender
* Osteoarthritis, rheumatoid arthritis, avascular necrosis

Exclusion Criteria:

* Severe allergy to antibiotic used in the study
* Severe renal dysfunction (eGFR \< 30 ml/min)
* Methicillin-resistant Staphylococcus aureus (MRSA) colonization
* participants who require revision surgery

Study Location

Dr, Adam Hart
Dr, Adam Hart
Montréal, Quebec
Canada

Contact Study Team

Backup Contact

Karen Smith

[email protected]
514-934-1934
Primary Contact

Adam Hart, MD

[email protected]
514-934-1934
Study Sponsored By
McGill University Health Centre/Research Institute of the McGill University Health Centre
Participants Required
More Information
Study ID: NCT05604157