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Linezolid: a review of its use in the management of serious gram-positive infections.

机译:利奈唑胺:综述其在治疗严重革兰氏阳性感染中的用途。

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摘要

Linezolid is the first of a new class of antibacterial drugs, the oxazolidinones. It has inhibitory activity against a broad range of gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), glycopeptide-intermediate S. aureus (GISA), vancomycin-resistant enterococci (VRE) and penicillin-resistant Streptococcus pneumoniae. The drug also shows activity against certain anaerobes, including Clostridium perfringens, C. difficile, Peptostreptococcus spp. and Bacteroidesfragilis. In controlled phase III studies, linezolid was as effective as vancomycin in the treatment of patients with infections caused by methicillin-resistant staphylococci and also demonstrated efficacy against infections caused by VRE. Further phase III studies have demonstrated that linezolid is an effective treatment for patients with nosocomial pneumonia, for hospitalised patients with community-acquired pneumonia, and for patients with complicated skin or soft tissue infections (SSTIs). In these studies, linezolid was as effective as established treatments, including third-generation cephalosporins in patients with pneumonia, and oxacillin in patients with complicated SSTIs. Oral linezolid 400 or 600mg twice daily was as effective as clarithromycin 250mg twice daily or cefpodoxime proxetil 200mg twice daily in the treatment of patients with uncomplicated SSTIs or community-acquired pneumonia. Linezolid is a generally well tolerated drug. The most frequently reported adverse events in linezolid recipients were diarrhoea, headache, nausea and vomiting. Thrombocytopenia was also documented in a small proportion (about 2%) of patients treated with the drug. CONCLUSIONS: Linezolid has good activity against gram-positive bacteria, particularly multidrug resistant strains of S. aureus (including GISA), Enterococcus faecium and E. faecalis (including VRE). In controlled clinical trials, linezolid was as effective as vancomycin in eradicating infections caused by methicillin-resistant Staphylococcus spp. and has demonstrated efficacy against infections caused by VRE. As the level of resistance to vancomycin increases among S. aureus and enterococci, linezolid is poised to play an important role in the management of serious gram-positive infections.
机译:利奈唑胺是新型抗菌药物中的第一个,恶唑烷酮。它对多种革兰氏阳性细菌具有抑制活性,包括耐甲氧西林的金黄色葡萄球菌(MRSA),糖肽中间的金黄色葡萄球菌(GISA),耐万古霉素的肠球菌(VRE)和耐青霉素的肺炎链球菌。该药还显示出对某些厌氧菌的活性,包括产气荚膜梭状芽孢杆菌,艰难梭菌,Peptostreptococcus spp。和脆弱拟杆菌。在III期对照研究中,利奈唑胺在治疗耐甲氧西林葡萄球菌感染的患者中与万古霉素一样有效,并且还显示出对VRE感染的疗效。进一步的III期研究表明,利奈唑胺对医院内肺炎患者,社区获得性肺炎住院患者以及复杂的皮肤或软组织感染(SSTI)患者有效。在这些研究中,利奈唑胺与已确立的治疗方法一样有效,包括肺炎患者的第三代头孢菌素和复杂SSTI患者的奥沙西林。每日两次口服利奈唑胺400或600mg与单纯性SSTI或社区获得性肺炎的治疗效果一样,每天两次,克拉一次霉素250mg克拉霉素或头孢泊肟肟200mg每天两次。利奈唑胺是一种耐受性良好的药物。利奈唑胺接受者中最常报告的不良事件是腹泻,头痛,恶心和呕吐。在使用该药物治疗的患者中,也有少量(约2%)记录有血小板减少症。结论:利奈唑胺对革兰氏阳性细菌具有良好的活性,特别是对金黄色葡萄球菌(包括GISA),粪肠球菌和粪肠球菌(包括VRE)具有多重耐药性。在对照临床试验中,利奈唑胺在根除耐甲氧西林葡萄球菌引起的感染方面与万古霉素一样有效。并已证明对VRE引起的感染有效。随着金黄色葡萄球菌和肠球菌对万古霉素的耐药性水平提高,利奈唑胺有望在严重的革兰氏阳性感染的治疗中发挥重要作用。

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