Harwood P J, Talbot C, Dimoutsos M, Sunderland G, Shaw D, Wilcox M H, Giannoudis P V
Academic Department of Orthopaedic Trauma Surgery, Leeds University, UK.
Injury. 2006 Sep;37(9):818-26. doi: 10.1016/j.injury.2006.02.007. Epub 2006 Apr 18.
In infections following orthopaedic surgery, isolated staphylococci are reported to be methicillin resistant (MRSA) in up to 50% of cases. Linezolid, the first in a new class of antibiotics, has excellent efficacy against gram positive organisms that are resistant to other therapies and is 100% orally bioavailable. We report early results of its use for the treatment of resistant infections in orthopaedic practice. Infections were characterised according to the UK Nosocomial Infections National Surveillance Service classification of surgical infections as superficial, deep or organ/space. Osteomyelitis, joint sepsis and deep infection involving orthopaedic implants were included into the final category. Outcome was recorded as clinical, microbiological and blood parameter cure or fail. Over the 12-month study period, 54 patients received linezolid therapy, 41% of these had significant co-morbidity that might affect their ability to fight infection. Sixty-seven percent of infections were in association with implanted metal work. The majority of patients were treated with vancomycin for a short period before linezolid was used as oral 'switch' therapy for longer-term administration, allowing early discharge in all cases. MRSA was isolated in 87% of the patients treated. The mean length of linezolid therapy was 39 days (2-151). Clinical success was achieved in 90% of patients overall. Though there were no life-threatening complications, adverse event rates were significantly higher than those recorded in the literature, with 19% of patients needing to cease therapy. Linezolid offers an alternative to traditional treatments for resistant infections and can facilitate early discharge. Patients need to be monitored closely, particularly where long-term therapy is planned.
在骨科手术后的感染中,据报道分离出的葡萄球菌在高达50%的病例中对甲氧西林耐药(MRSA)。利奈唑胺是新型抗生素中的首个药物,对耐其他疗法的革兰氏阳性菌具有出色疗效,且口服生物利用度达100%。我们报告了其在骨科实践中用于治疗耐药感染的早期结果。感染根据英国医院感染国家监测服务机构对手术感染的分类分为表浅、深部或器官/腔隙感染。骨髓炎、关节脓毒症以及涉及骨科植入物的深部感染归入最后一类。结果记录为临床、微生物学和血液参数方面的治愈或未治愈。在为期12个月的研究期间,54例患者接受了利奈唑胺治疗,其中41%有严重合并症,这可能影响其抗感染能力。67%的感染与植入的金属器械有关。大多数患者在使用利奈唑胺作为长期口服“转换”疗法之前短期使用了万古霉素,从而使所有病例均能早期出院。在接受治疗的患者中87%分离出了MRSA。利奈唑胺治疗的平均时长为39天(2 - 151天)。总体上90%的患者取得了临床成功。虽然没有危及生命的并发症,但不良事件发生率显著高于文献记载,19%的患者需要停止治疗。利奈唑胺为耐药感染的传统治疗提供了一种替代方案,并能促进早期出院。需要密切监测患者,尤其是在计划进行长期治疗的情况下。