Bassetti Matteo, Vitale Francesco, Melica Giovanna, Righi Elda, Di Biagio Antonio, Molfetta Luigi, Pipino Francesco, Cruciani Mario, Bassetti Dante
Infectious Diseases Department, University of Genoa School of Medicine, San Martino Hospital, Genoa, Italy.
J Antimicrob Chemother. 2005 Mar;55(3):387-90. doi: 10.1093/jac/dki016. Epub 2005 Feb 10.
To investigate the clinical efficacy and safety of linezolid in the treatment of Gram-positive prosthetic hip and knee infections.
A retrospective evaluation of patients hospitalized in the Department of Infectious Diseases of San Martino Hospital in Genoa with the diagnosis of Gram-positive prosthetic joint infection and treated with intravenous and/or oral linezolid. Primary end points were the patient clinical outcome at the end of treatment and at long-term follow-up (up to 12 months after the end of treatment).
Between May 1999 and September 2003, 20 patients with prosthetic joint infection were treated with linezolid. Pathogens isolated were: methicillin-resistant Staphylococcus aureus (MRSA), 14 strains; methicillin-resistant coagulase-negative staphylococci, five strains; and Enterococcus spp., one strain. The overall duration of treatment was 7.2 +/- 2 weeks (range 6-10 weeks). Patients were given intravenous therapy for 3-7 days as inpatients, then were changed as outpatients to oral therapy under weekly laboratory testing. At long-term follow-up (1 year), we observed four cases of failure due to relapsing infections. The other 16 patients treated with linezolid did not need further surgical substitution of prosthesis or surgical joint revision. Linezolid was well tolerated, and no drug-related events leading to discontinuation of treatment were recorded.
Our data indicate that linezolid may be an effective alternative therapy for orthopaedic infections caused by Gram-positive resistant pathogens and that a prospective and comparative evaluation of linezolid in this setting is necessary.
探讨利奈唑胺治疗革兰阳性菌所致人工髋关节和膝关节感染的临床疗效及安全性。
对热那亚圣马蒂诺医院传染病科收治的诊断为革兰阳性菌人工关节感染并接受静脉和/或口服利奈唑胺治疗的患者进行回顾性评估。主要终点为治疗结束时及长期随访(治疗结束后长达12个月)时的患者临床结局。
1999年5月至2003年9月,20例人工关节感染患者接受了利奈唑胺治疗。分离出的病原体为:耐甲氧西林金黄色葡萄球菌(MRSA),14株;耐甲氧西林凝固酶阴性葡萄球菌,5株;肠球菌属,1株。总体治疗时间为7.2±2周(范围6 - 10周)。患者住院时接受3 - 7天的静脉治疗,然后转为门诊患者,在每周实验室检查的情况下接受口服治疗。在长期随访(1年)时,我们观察到4例因感染复发导致治疗失败的病例。其他16例接受利奈唑胺治疗的患者无需进一步手术更换假体或进行手术关节翻修。利奈唑胺耐受性良好,未记录到导致治疗中断的药物相关事件。
我们的数据表明,利奈唑胺可能是治疗革兰阳性耐药病原体所致骨科感染的一种有效替代疗法,并且有必要对利奈唑胺在这种情况下进行前瞻性和对比性评估。