Vila Andrea, Pagella Hugo, Amadio Claudio, Leiva Alejandro
Department of Infectious Diseases, Hospital Italiano, Mendoza, Argentina.
Department of Microbiology Laboratories, Hospital Italiano, Mendoza, Argentina.
Infect Chemother. 2016 Dec;48(4):324-329. doi: 10.3947/ic.2016.48.4.324. Epub 2016 Nov 8.
Prosthesis retention is not recommended for multidrug-resistant Acinetobacter prosthetic joint infection due to its high failure rate. Nevertheless, replacing the prosthesis implies high morbidity and prolonged hospitalization. Although tigecycline is not approved for the treatment of prosthetic joint infection due to multidrug resistant Acinetobacter baumannii, its appropriate use may preclude prosthesis exchange. Since the area under the curve divided by the minimum inhibitory concentration is the best pharmacodynamic predictor of its efficacy, we used tigecycline at high dose, in order to optimize its efficacy and achieve implant retention in 3 patients who refused prosthesis exchange. All patients with prosthetic joint infections treated at our Institution are prospectively registered in a database. Three patients with early prosthetic joint infection of total hip arthroplasty due to multidrug resistant A. baumannii were treated with debridement, antibiotics and implant retention, using a high maintenance dose of tigecycline (100 mg every 12 hours). The cases were retrospectively reviewed. All patients signed informed consent for receiving off-label use of tigecycline. Tigecycline was well tolerated, allowing its administration at high maintenance dose for a median of 40 days (range 30-60). Two patients were then switched to minocycline at standard doses for a median of 3.3 months in order to complete treatment. Currently, none of the patients showed relapse. Increasing the dose of tigecycline could be considered as a means to better attain pharmacodynamic targets in patients with severe or difficult-to-treat infections. Tigecycline at high maintenance dose might be useful when retention of the implant is attempted for treatment for prosthetic joint infections due to multidrug resistant Acinetobacter. Although this approach might be promising, off-label use of tigecycline should be interpreted cautiously until prospective data are available. Tigecycline is probably under-dosed for the treatment of implant and biofilm associated infections.
由于多药耐药鲍曼不动杆菌所致人工关节感染的假体保留失败率高,故不建议采用。然而,更换假体意味着高发病率和延长住院时间。尽管替加环素未被批准用于治疗多药耐药鲍曼不动杆菌所致人工关节感染,但其合理使用可能避免假体置换。由于曲线下面积除以最低抑菌浓度是其疗效的最佳药效学预测指标,我们对3例拒绝假体置换的患者使用高剂量替加环素,以优化其疗效并实现植入物保留。在我们机构接受治疗的所有人工关节感染患者均前瞻性地登记在一个数据库中。3例因多药耐药鲍曼不动杆菌导致全髋关节置换术后早期人工关节感染的患者,采用清创、抗生素治疗及植入物保留,使用高维持剂量的替加环素(每12小时100mg)。对这些病例进行了回顾性分析。所有患者均签署了接受替加环素超说明书用药的知情同意书。替加环素耐受性良好,允许以高维持剂量给药,中位时间为40天(范围30 - 60天)。然后,2例患者换用标准剂量的米诺环素,中位时间为3.3个月以完成治疗。目前,所有患者均未出现复发。增加替加环素剂量可被视为在重症或难治性感染患者中更好地达到药效学目标的一种方法。高维持剂量的替加环素在尝试保留植入物以治疗多药耐药鲍曼不动杆菌所致人工关节感染时可能有用。尽管这种方法可能很有前景,但在有前瞻性数据可用之前,替加环素的超说明书用药应谨慎解读。替加环素治疗植入物及生物膜相关感染的剂量可能不足。