首页> 外文期刊>Journal of Internal Medicine >Levofloxacin does not decrease mortality in Staphylococcus aureus bacteraemia when added to the standard treatment: a prospective and randomized clinical trial of 381 patients.
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Levofloxacin does not decrease mortality in Staphylococcus aureus bacteraemia when added to the standard treatment: a prospective and randomized clinical trial of 381 patients.

机译:当将左氧氟沙星加入标准治疗后,不会降低金黄色葡萄球菌菌血症的死亡率:这是一项针对381例患者的前瞻性随机临床试验。

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OBJECTIVES: To study whether levofloxacin, added to standard treatment, could reduce the high mortality and complication rates in Staphylococcus aureus bacteraemia. DESIGN: A prospective randomized multicentre trial from January 2000 to August 2002. SETTING: Thirteen tertiary care or university hospitals in Finland. SUBJECTS: Three hundred and eighty-one adult patients with S. aureus bacteraemia. Patients with meningitis, and those with fluoroquinolone- or methicillin-resistant S. aureus were excluded. INTERVENTIONS: Standard treatment (mostly semisynthetic penicillin) (n = 190) or that combined with levofloxacin (n = 191). Supplementary rifampicin was recommended if deep infection was suspected. MAIN OUTCOME MEASURES: Primary end-points were mortality at 28 days and at 3 months. Clinical and laboratory parameters were analysed as secondary end-points. RESULTS: Adding levofloxacin to the standard treatment offered no survival benefit. Case fatality rates were 14% in both groups at 28 days, and 21% in the standard treatment and 18% in the levofloxacin group at 3 months. Levofloxacin combination did not differ from the standard treatment in the number of complications, time to defervescence, decrease in serum C-reactive protein concentration or length of antibiotic treatment. Deep infection was found in 84% of patients within 1 week following randomization with no difference between the treatment groups. At 3 months, the case fatality rate for patients with deep infection was 17% amongst those who received rifampicin versus 38% for those without rifampicin (P < 0.001, odds ratio = 3.06, 95% confidence intervals = 1.69-5.54). CONCLUSIONS: Levofloxacin combined with standard treatment in S. aureus bacteraemia did not decrease mortality or the incidence of deep infections, nor did it speed up recovery. Interestingly, deep infections in S. aureus bacteraemia appeared to be more common than previously reported.
机译:目的:研究左氧氟沙星加标准治疗是否可以降低金黄色葡萄球菌菌血症的高死亡率和并发症发生率。设计:2000年1月至2002年8月的一项前瞻性随机多中心试验。地点:芬兰的13家三级护理或大学医院。受试者:381名成年金黄色葡萄球菌菌血症患者。脑膜炎患者和耐氟喹诺酮或耐甲氧西林金黄色葡萄球菌的患者被排除在外。干预措施:标准治疗(主要为半合成青霉素)(n = 190)或与左氧氟沙星联合治疗(n = 191)。如果怀疑有深层感染,建议补充利福平。主要观察指标:主要终点是28天和3个月时的死亡率。临床和实验室参数作为次要终点进行分析。结果:在标准治疗中添加左氧氟沙星无生存益处。两组在28天时的病死率为14%,在标准治疗中3个月时的病死率为21%,在左氧氟沙星组中为18%。左氧氟沙星组合与标准治疗在并发症发生次数,退热时间,血清C反应蛋白浓度降低或抗生素治疗时间方面无差异。随机分配后1周内,在84%的患者中发现了深部感染,治疗组之间无差异。在3个月时,接受利福平治疗的深层感染患者的病死率为17%,而未接受利福平治疗的患者的病死率为38%(P <0.001,优势比= 3.06,95%置信区间= 1.69-5.54)。结论:左氧氟沙星联合标准治疗金黄色葡萄球菌菌血症未降低死亡率或深层感染的发生率,也未加快恢复速度。有趣的是,金黄色葡萄球菌菌血症的深部感染似乎比以前报道的更为普遍。

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