Antibiotic Prophylaxis in High-Risk Arthroplasty Patients
Infections Joint Prosthetic, Overweight or Obesity, MSSA Colonization
About this trial
This is an interventional prevention trial for Infections Joint Prosthetic focused on measuring total hip arthroplasty, total knee arthroplasty, hip replacement, knee replacement, periprosthetic joint infection, prophylaxis, antibiotics
Eligibility Criteria
Inclusion Criteria:
- Undergoing elective, primary total hip or total knee arthroplasty
- Between the ages of 18-99
- Has one or more of the following high risk criteria: body mass index (BMI) greater than 35kg/m^2, diagnosis of diabetes, active tobacco user, chronic kidney disease (estimated glomerular filtration (eGFR) < 60 mL/min/1.73 m2), nasal colonization of MRSA and/or MSSA or autoimmune/inflammatory disease.
Exclusion Criteria:
- Younger than 18 years old
- Undergoing a revision hip or knee arthroplasty
- Will have a subsequent total joint arthroplasty performed within 12 weeks of study enrollment
- Patient is discharged the same day as primary THA or TKA
- History of clostridium difficile colitis
- Undergoing non-elective procedure
- Hemiarthroplasty
- Unicompartmental knee arthroplasty
- Simultaneous bilateral total hip or knee arthroplasty
- Pregnant
- Unable to provide written consent
Sites / Locations
- University of Iowa Hospitals & Clinics
- Mayo Clinic
Arms of the Study
Arm 1
Arm 2
Active Comparator
No Intervention
Additional Antibiotic Group
Control Group - No Additional Antibiotic
Patients will receive an oral antibiotic to be started after completion of standard perioperative antibiotics following primary hip or knee arthroplasty. Oral antibiotic will either be a first-generation cephalosporin (Cefadroxil or Cephalexin) or Doxycycline based upon patient allergies, kidney function and result of nasal colonization testing for MRSA.
Patients will receive standard perioperative antibiotics following primary hip or knee arthroplasty and no additional antibiotics.