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首页> 外文期刊>International journal of antimicrobial agents >Moxifloxacin monotherapy versus β-lactam-based standard therapy for community-acquired pneumonia: A meta-analysis of randomised controlled trials
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Moxifloxacin monotherapy versus β-lactam-based standard therapy for community-acquired pneumonia: A meta-analysis of randomised controlled trials

机译:莫西沙星单一疗法与以β-内酰胺为基础的标准疗法治疗社区获得性肺炎的随机对照试验的荟萃分析

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The aim of this study was to compare more conclusively the efficacy and safety of moxifloxacin, a new respiratory fluoroquinolone antibiotic, with β-lactam-based standard therapy, which has been reported to possess good efficacy for community-acquired pneumonia (CAP). A meta-analysis of randomised controlled trials (RCTs) identified in PubMed, the Cochrane Library and Embase was performed. Seven RCTs, involving 3903 patients, were included in the meta-analysis. Moxifloxacin monotherapy was associated with similar clinical treatment success rates [clinically evaluable population, odds ratio (OR)=1.15, 95% confidence interval (CI) 0.81-1.64; intention-to-treat population, OR=1.11, 95% CI 0.86-1.42] and similar mortality (OR=0.98, 95% CI 0.66-1.46) compared with β-lactam-based standard therapy for CAP. Microbiological treatment success rates in the moxifloxacin group were significantly higher than in the β-lactam-based therapy group with a statistical margin (OR=1.69, 95% CI 1.02-2.80). No difference was found regarding the incidence of adverse events and serious adverse events between moxifloxacin and β-lactam-based standard therapy. This meta-analysis provides evidence that moxifloxacin not only can be used as effectively and safely as β-lactam-based standard therapy for CAP but also possesses a favourable pathogen eradication rate. The once-daily dosing of moxifloxacin monotherapy may be a useful alternative for β-lactam-based standard therapy.
机译:这项研究的目的是更确切地比较一种新型呼吸道氟喹诺酮类抗生素莫西沙星与基于β-内酰胺的标准疗法的疗效和安全性,据报道该疗法对社区获得性肺炎(CAP)具有良好的疗效。对在PubMed,Cochrane文库和Embase中鉴定的随机对照试验(RCT)进行了荟萃分析。荟萃分析包括七个涉及3903名患者的RCT。莫西沙星单药治疗与相似的临床治疗成功率相关[临床可评估人群,优势比(OR)= 1.15,95%置信区间(CI)0.81-1.64;与基于β-内酰胺的CAP标准疗法相比,意向性治疗人群OR = 1.11,95%CI 0.86-1.42]和相似的死亡率(OR = 0.98,95%CI 0.66-1.46)。莫西沙星组的微生物学治疗成功率显着高于基于β-内酰胺的治疗组,具有统计学上的优势(OR = 1.69,95%CI 1.02-2.80)。在莫西沙星和基于β-内酰胺的标准疗法之间,不良事件和严重不良事件的发生率没有差异。这项荟萃分析提供的证据表明,莫西沙星不仅可以像基于β-内酰胺的CAP标准疗法一样安全有效地使用,而且具有良好的病原体清除率。莫西沙星单一疗法的每日一次剂量可能是基于β-内酰胺的标准疗法的有用替代方法。

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