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Cochrane meta-analysis: teicoplanin versus vancomycin for proven or suspected infection

机译:Cochrane荟萃分析:替考拉宁与万古霉素用于已证实或怀疑的感染

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ABSTRACTObjective:To compare efficacy and safety of vancomycin versusteicoplanin in patients with proven or suspected infection.Methods:Data Sources: Cochrane Renal Group's Specialized Register, CENTRAL, MEDLINE, EMBASE, nephrology textbooks and review articles. Inclusion criteria: Randomized controlled trials in any language comparing teicoplanin to vancomycin for patients with proven or suspected infection. Data extraction: Two authors independently evaluated methodological quality and extracted data. Study investigators were contacted for unpublished information. A random effect model was used to estimate the pooled risk ratio (RR) with 95% confidence interval (CI).Results:A total of 24 studies (2,610 patients) were included. The drugs had similar rates of clinical cure (RR: 1.03; 95%CI: 0.98-1.08), microbiological cure (RR: 0.98; 95%CI: 0.93-1.03) and mortality (RR: 1.02; 95%CI: 0.79-1.30). Teicoplanin had lower rates of skin rash (RR: 0.57; 95%CI: 0.35-0.92), red man syndrome (RR: 0.21; 95%CI: 0.08-0.59) and total adverse events (RR: 0.73; 95%CI: 0.53-1.00). Teicoplanin reduced the risk of nephrotoxicity (RR: 0.66; 95%CI: 0.48-0.90). This effect was consistent for patients receiving aminoglycosides (RR: 0.51; 95%CI: 0.30-0.88) or having vancomycin doses corrected by serum levels (RR: 0.22; 95%CI: 0.10-0.52). There were no cases of acute kidney injury needing dialysis.Limitations:Studies lacked a standardized definition for nephrotoxicity.Conclusions:Teicoplanin and vancomycin are equally effective; however the incidence of nephrotoxicity and other adverse events was lower with teicoplanin. It may be reasonable to consider teicoplanin for patients at higher risk for acute kidney injury.
机译:摘要目的:比较万古霉素和替考拉宁在已证实或怀疑感染的患者中的有效性和安全性。方法:数据来源:Cochrane肾病集团的专门登记册,CENTRAL,MEDLINE,EMBASE,肾病学教科书和评论文章。纳入标准:以任何语言进行的随机对照试验,比较替考拉宁和万古霉素对已证实或怀疑感染的患者的影响。数据提取:两位作者独立评估了方法学质量并提取了数据。与研究调查人员联系以获取未发布的信息。结果:共纳入24项研究(2,610例患者),采用随机效应模型评估95%可信区间(CI)的合并风险比(RR)。这些药物的临床治愈率(RR:1.03; 95%CI:0.98-1.08),微生物学治愈率(RR:0.98; 95%CI:0.93-1.03)和死亡率(RR:1.02; 95%CI:0.79- 1.30)。 Teicoplanin的皮疹发生率较低(RR:0.57; 95%CI:0.35-0.92),红皮病综合征(RR:0.21; 95%CI:0.08-0.59)和总不良事件(RR:0.73; 95%CI: 0.53-1.00)。 Teicoplanin降低了肾毒性的风险(RR:0.66; 95%CI:0.48-0.90)。对于接受氨基糖苷类药物(RR:0.51; 95%CI:0.30-0.88)或通过血清水平校正的万古霉素剂量(RR:0.22; 95%CI:0.10-0.52)的患者,这种作用是一致的。局限性:研究缺乏对肾毒性的标准化定义。结论:替考拉宁和万古霉素同等有效。但是替考拉宁的肾毒性和其他不良事件发生率较低。对于有较高急性肾损伤风险的患者考虑替考拉宁可能是合理的。

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