Intraosseous Regional Administration of Vancomycin in Primary Total Knee Arthroplasty Does Not Increase the Risk of Vancomycin-Associated Complications

被引:18
作者
Klasan, Antonio [1 ,2 ,3 ]
Patel, Chetan Kumar [1 ]
Young, Simon William [1 ]
机构
[1] North Shore Hosp, 124 Shakespeare Rd, Auckland 0620, New Zealand
[2] Kepler Univ Hosp GmbH, Dept Orthopaed & Traumatol, Linz, Austria
[3] Johannes Kepler Univ Linz, Linz, Austria
关键词
total knee arthroplasty; periprosthetic joint infection; vancomycin; adverse effects; kidney injury; red man syndrome; RED MAN SYNDROME; HIGHER TISSUE CONCENTRATIONS; PROPHYLACTIC ANTIBIOTICS; INDUCED NEUTROPENIA; INFECTION; HIP; EPIDEMIOLOGY; RESISTANCE; REVISION; TKA;
D O I
10.1016/j.arth.2020.12.034
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: Periprosthetic joint infection (PJI) after total knee arthroplasty (TKA) is a rare but major complication. Owing to an increasing antibiotic resistance in bacteria causing PJI, vancomycin has been investigated as a prophylactic agent. Intraosseous regional administration (IORA) of vancomycin achieves significantly higher local tissue concentrations than systemic administration. There are limited data on IORA of vancomycin with respect to vancomycin-associated complications. Methods: Single-surgeon retrospective review of primary TKA was performed between January 2015 and May 2019. All patients received 500 mg of IORA of vancomycin after tourniquet inflation and 3 x 1 g intravenous cefazolin in 24 hrs. Preoperative data collected included age, gender, body mass index, American Society of Anesthesiologists (ASA) score, diabetes, and chronic kidney disease (CKD). We documented in-hospital complications and complications requiring readmission within 12 months. Primary outcome measures were the incidence of acute kidney injury (AKI), `red man syndrome' (RMS), and neutropenia. The secondary outcome measure was PJI incidence. Results: We identified 631 primary TKAs in 556 patients, of which 331 received IORA. The mean age was 67.7 +/- 8.7 years, and 57.8% were women. CKD was prevalent in 17.2% of the cohort. AKI occurred in 25 (3.9%) cases. After controlling for covariates, CKD was the only significant predictor of AKI (odds ratio = 3.035, P = .023). RMS and neutropenia were not observed in this cohort. The 90-day PJI rate was 0%, and the 1-year PJI rate was 0.2%. Conclusions: Low-dose IORA of vancomycin in addition to standard intravenous systemic cefazolin prophylaxis in TKA is safe without significant adverse effects of vancomycin such as AKI, RMS, or neutropenia. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:1633 / 1637
页数:5
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