Local Application of Vancomycin in One-Stage Revision of Prosthetic Joint Infection Caused by Methicillin-Resistant Staphylococcus aureus
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Published on: March 14, 2019
Jian Wei1, Yinxian Wen1, Kai Tong1
1Department of Joint Surgery and Sports Medicine, Zhongnan Hospital of Wuhan Universitygrid.413247.7, Wuhan, China.
Abstract:
The rate of eradication of periprosthetic joint infection (PJI) caused by methicillin-resistant Staphylococcus aureus (MRSA) is still not satisfactory with systemic vancomycin administration after one-stage revision arthroplasty. This study aimed to explore the effectiveness and safety of intraarticular (IA) injection of vancomycin in the control of MRSA PJI after one-stage revision surgery in a rat model. Two weeks of intraperitoneal (IP) and/or IA injection of vancomycin was used to control the infection after one-stage revision surgery. The MRSA PJI rats treated with IA injection of vancomycin showed better outcomes in skin temperature, bacterial counts, biofilm on the prosthesis, serum α1-acid glycoprotein levels, residual bone volume, and inflammatory reaction in the joint tissue, compared with those treated with IP vancomycin, while the rats treated with IP and IA administration showed the best outcomes. However, only the IP and IA administration of vancomycin could eradicate MRSA. Minimal changes in renal pathology were observed in the IP and IP plus IA groups but not in the IA group, while no obvious changes were observed in the liver or in levels of serum markers, including creatinine, alanine aminotransferase, and aspartate aminotransferase. Therefore, IA use of vancomycin is effective and safe in the MRSA PJI rat model and is better than systemic administration, while IA and systemic vancomycin treatment could eradicate the infection with a 2-week treatment course.
Insights
Intraarticular vancomycin injections improve outcomes for methicillin-resistant Staphylococcus aureus periprosthetic joint infections in rats. Combined intraarticular and systemic vancomycin eradicated infection with minimal side effects.
Area of Science:
- Orthopedics
- Infectious Diseases
- Pharmacology
Background:
- Periprosthetic joint infection (PJI) caused by methicillin-resistant Staphylococcus aureus (MRSA) presents a significant challenge.
- Current systemic vancomycin treatment for MRSA PJI after one-stage revision arthroplasty has unsatisfactory eradication rates.
Purpose of the Study:
- To evaluate the efficacy and safety of intraarticular (IA) vancomycin injection compared to intraperitoneal (IP) vancomycin for controlling MRSA PJI in a rat model.
- To determine the optimal vancomycin administration route for MRSA PJI eradication.
Main Methods:
- A rat model of MRSA PJI was established following one-stage revision surgery.
- Animals received two weeks of either IP vancomycin, IA vancomycin, or a combination of both IP and IA vancomycin.
- Outcomes were assessed by measuring skin temperature, bacterial counts, biofilm formation, serum inflammatory markers, bone volume, and joint tissue inflammation.
Main Results:
- IA vancomycin treatment demonstrated superior outcomes in reducing infection markers compared to IP vancomycin alone.
- Combined IP and IA vancomycin administration yielded the best overall results.
- Only the combination therapy achieved complete MRSA eradication.
- Minimal renal pathology was observed in the IP and combined IP/IA groups, with no significant liver or serum marker changes.
Conclusions:
- Intraarticular vancomycin is an effective and safe adjunctive treatment for MRSA PJI in a rat model, outperforming systemic administration.
- Combined intraarticular and systemic vancomycin administration is necessary for complete MRSA eradication within a 2-week treatment course.
- This approach offers a promising strategy for managing challenging MRSA PJI cases.
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