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Antibiotic Prophylaxis in High-Risk Arthroplasty Patients

Primary Purpose

Infections Joint Prosthetic, Overweight or Obesity, MSSA Colonization

Status
Enrolling by invitation
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Cephalexin
Doxycycline
Cefadroxil
Sponsored by
Mayo Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Active Comparator

No Intervention

Arm Label

Additional Antibiotic Group

Control Group - No Additional Antibiotic

Arm Description

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.

Outcomes

Primary Outcome Measures

Periprosthetic joint infections
Defined by Musculoskeletal Infection Society (MSIS) criteria
Periprosthetic joint infections
Defined by Musculoskeletal Infection Society (MSIS) criteria

Secondary Outcome Measures

Wound complication
Defined by at least one of the following: surgical wound dehiscence, skin necrosis at the surgical site, persistent surgical wound drainage (fluid extrusion from the operative site occurring beyond 72 hours from index surgery), superficial surgical site infection treated with new prescription of antibiotics or a change in study antibiotics but not meeting criteria for periprosthetic joint infection.

Full Information

First Posted
March 3, 2020
Last Updated
June 26, 2023
Sponsor
Mayo Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT04297592
Brief Title
Antibiotic Prophylaxis in High-Risk Arthroplasty Patients
Official Title
Antibiotic Prophylaxis in High-Risk Arthroplasty Patients
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Enrolling by invitation
Study Start Date
June 11, 2020 (Actual)
Primary Completion Date
June 2025 (Anticipated)
Study Completion Date
June 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
To determine the effectiveness of a 7-day course of an oral, prophylactic antibiotic on the incidence of periprosthetic joint infection and wound complications following primary total hip and knee arthroplasty in a high-risk patient population.
Detailed Description
The purpose of this research study is to investigate whether a 7-day course of an oral, prophylactic antibiotic following elective, primary total hip and knee arthroplasty effectively decreases the risk of periprosthetic joint infection or wound complications following surgery in a patient population that is high-risk for these complications. Patient with one or more of the following risk factors are considered high-risk for periprosthetic joint infection and/or wound complications: body mass index over 35kg/m^2, diagnosis of diabetes, chronic kidney disease, active tobacco user, nasal colonization of methicillin-resistant Staphylococcus aureus and/or methicillin-sensitive Staphylococcus aureus, or autoimmune/inflammatory disease. Study participants will be randomized to either a 7-day course of an oral, prophylactic antibiotic following surgery or no additional antibiotic. All other standard perioperative total joint arthroplasty care will remain the same for both groups, including 24-hours of perioperative antibiotics. Outcomes assessed will include surgical wound complications occurring within 90-day of surgery and periprosthetic joint infection occurring within 90-day and 1-year of surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infections Joint Prosthetic, Overweight or Obesity, MSSA Colonization, MRSA, Chronic Kidney Diseases, Diabetes, Autoimmune Diseases, Inflammatory Disease, Tobacco Use
Keywords
total hip arthroplasty, total knee arthroplasty, hip replacement, knee replacement, periprosthetic joint infection, prophylaxis, antibiotics

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
4618 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Additional Antibiotic Group
Arm Type
Active Comparator
Arm Description
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.
Arm Title
Control Group - No Additional Antibiotic
Arm Type
No Intervention
Arm Description
Patients will receive standard perioperative antibiotics following primary hip or knee arthroplasty and no additional antibiotics.
Intervention Type
Drug
Intervention Name(s)
Cephalexin
Other Intervention Name(s)
Keflex
Intervention Description
500 mg oral tablet, 4 times daily for 7 days
Intervention Type
Drug
Intervention Name(s)
Doxycycline
Intervention Description
100 mg oral tablet, 2 times daily for 7 days
Intervention Type
Drug
Intervention Name(s)
Cefadroxil
Other Intervention Name(s)
Duricef
Intervention Description
500 mg oral tablet, 2 times daily for 7 days
Primary Outcome Measure Information:
Title
Periprosthetic joint infections
Description
Defined by Musculoskeletal Infection Society (MSIS) criteria
Time Frame
Within 90-days primary hip or knee arthroplasty
Title
Periprosthetic joint infections
Description
Defined by Musculoskeletal Infection Society (MSIS) criteria
Time Frame
Within 1-year of primary hip or knee arthroplasty
Secondary Outcome Measure Information:
Title
Wound complication
Description
Defined by at least one of the following: surgical wound dehiscence, skin necrosis at the surgical site, persistent surgical wound drainage (fluid extrusion from the operative site occurring beyond 72 hours from index surgery), superficial surgical site infection treated with new prescription of antibiotics or a change in study antibiotics but not meeting criteria for periprosthetic joint infection.
Time Frame
Within 90 days of primary hip or knee arthroplasty

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient is a candidate for elective, primary total hip arthroplasties (THA) or total knee arthroplasties (TKA). Patient is considered high-risk for developing Periprosthetic joint infections (PJI) based on having at least one of the following criteria: Body mass index (BMI) > 35 kg/m^2; Diagnosis of diabetes mellitus; Active tobacco smoker; Chronic kidney disease; Autoimmune disease; Nasal colonization with methicillin-resistant Staphylococcus aureus (MRSA) or methicillin-sensitive Staphylococcus aureus (MSSA). Exclusion Criteria: Inability to consume oral antibiotics. Allergy to antibiotic alternatives in the protocol. History of clostridium difficile colitis. Revision hip or knee arthroplasty procedure. Non-elective surgery. Hemiarthroplasty. Unicompartmental knee arthroplasty. Simultaneous bilateral THA or TKA. Will have subsequent THA or TKA within 12 weeks of the index study procedure. Pregnant.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicholas Bedard, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Iowa Hospitals & Clinics
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55902
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30562290
Citation
Inabathula A, Dilley JE, Ziemba-Davis M, Warth LC, Azzam KA, Ireland PH, Meneghini RM. Extended Oral Antibiotic Prophylaxis in High-Risk Patients Substantially Reduces Primary Total Hip and Knee Arthroplasty 90-Day Infection Rate. J Bone Joint Surg Am. 2018 Dec 19;100(24):2103-2109. doi: 10.2106/JBJS.17.01485.
Results Reference
background
PubMed Identifier
28722231
Citation
Li B, Webster TJ. Bacteria antibiotic resistance: New challenges and opportunities for implant-associated orthopedic infections. J Orthop Res. 2018 Jan;36(1):22-32. doi: 10.1002/jor.23656. Epub 2017 Aug 11.
Results Reference
background
PubMed Identifier
22554729
Citation
Kurtz SM, Lau E, Watson H, Schmier JK, Parvizi J. Economic burden of periprosthetic joint infection in the United States. J Arthroplasty. 2012 Sep;27(8 Suppl):61-5.e1. doi: 10.1016/j.arth.2012.02.022. Epub 2012 May 2.
Results Reference
background
Links:
URL
https://www.mayo.edu/research/clinical-trials
Description
Mayo Clinic Clinical Trials

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Antibiotic Prophylaxis in High-Risk Arthroplasty Patients

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