Razonable Raymund R, Osmon Douglas R, Steckelberg James M
Division of Infectious Diseases and Internal Medicine, Mayo Clinic College of Medicine, Rochester, Minn 55905, USA.
Mayo Clin Proc. 2004 Sep;79(9):1137-44. doi: 10.4065/79.9.1137.
To assess the clinical and bacteriological efficacy and the safety and tolerability profile of linezolid when used as the primary component of a combined surgical and antimicrobial treatment strategy for orthopedic infections.
We retrospectively reviewed medical records to obtain clinical, bacteriological, and safety outcomes of 20 consecutive patients who took linezolid for the treatment of orthopedic infections between April 1, 2000, and November 30, 2002.
Twenty patients received linezolid therapy for microbiologically confirmed orthopedic infections due to gram-positive cocci during the 32-month study period. Fifteen patients (75%) had infections involving orthopedic hardware; in 10 of these patients, the hardware was removed. All 20 patients underwent surgical débridement. At a mean follow-up of 276 days, 11 patients (55%) achieved clinical cure, 7 (35%) had clinical improvement but received long-term antimicrobial suppressive therapy, 1 (5%) had clinical relapse after discontinuing linezolid treatment, and 1 (5%) died of a cause unrelated to linezolid treatment. Bacterial persistence was documented in 3 patients (15%), all of whom were Infected with methicillin-resistant Staphylococcus aureus. Eight patients (40%) developed reversible myelosuppression, 1 (5%) had irreversible peripheral neuropathy, and 2 (10%) discontinued linezolid treatment because of pancytopenia or urticaria.
Oral linezolid may be an effective alternative therapy for orthopedic infections due to linezolid-susceptible gram-positive bacteria in patients who are unable to take other antimicrobial drugs because of drug allergy or Intolerance or antimicrobial resistance.
评估利奈唑胺作为骨科感染手术及抗菌联合治疗策略的主要组成部分时的临床和细菌学疗效以及安全性和耐受性。
我们回顾性分析了2000年4月1日至2002年11月30日期间连续20例服用利奈唑胺治疗骨科感染患者的病历,以获取临床、细菌学及安全性结果。
在32个月的研究期间,20例患者因革兰氏阳性球菌引起的经微生物学确诊的骨科感染接受了利奈唑胺治疗。15例患者(75%)的感染涉及骨科植入物;其中10例患者的植入物被取出。所有20例患者均接受了手术清创。平均随访276天时,11例患者(55%)实现临床治愈,7例(35%)有临床改善但接受了长期抗菌抑制治疗,1例(5%)在停用利奈唑胺治疗后出现临床复发,1例(5%)死于与利奈唑胺治疗无关的原因。3例患者(15%)出现细菌持续存在,所有这些患者均感染耐甲氧西林金黄色葡萄球菌。8例患者(40%)出现可逆性骨髓抑制,1例(5%)出现不可逆性周围神经病变,2例(10%)因全血细胞减少或荨麻疹而停用利奈唑胺治疗。
对于因药物过敏、不耐受或抗菌药物耐药而无法使用其他抗菌药物的患者,口服利奈唑胺可能是治疗对利奈唑胺敏感的革兰氏阳性菌引起的骨科感染的有效替代疗法。