Department of Clinical Pharmacology, Chinese People's Liberation Army General Hospital, 28 Fuxing Road, Beijing 100853, PR China.
BMC Infect Dis. 2009 Dec 2;9:193. doi: 10.1186/1471-2334-9-193.
Ertapenem, a new carbapenem with a favorable pharmacokinetic profile, has been approved for the treatment of complicated intra-abdominal Infections (cIAIs), acute pelvic infections (APIs) and complicated skin and skin-structure infections (cSSSIs). The aim of this study is to compare the efficacy and safety of ertapenem with piperacillin/tazobactam, which has been reported to possess good efficacy for the treatment of these complicated infections.
We performed a meta-analysis of randomized controlled trials identified in PubMed, Cochrane library and Embase that compared the efficacy and safety of ertapenem with piperacillin/tazobactam for the treatment of complicated infections including cIAIs, APIs, cSSSIs. The primary efficacy outcome was clinical treatment success assessed at the test-of-cure visit. The primary safety outcome was drug related clinical and laboratory adverse events occurred during the treatment and the post-treatment period.
Six RCTs, involving 3161 patients, were included in our meta-analysis. Ertapenem was associated similar clinical treatment success with piperacillin/tazobactam for complicated infections treatment (clinically evaluable population, 1937 patients, odds ratios: 1.15, 95% confidence intervals: 0.89-1.49; modified intention to treat population, 2855 patients, odds ratios: 1.03, 95% confidence intervals: 0.87-1.22). All of secondary efficacy outcomes analysis obtained similar findings with clinical treatment success. No difference was found about the incidence of drug related adverse events between ertapenem and piperacillin/tazobactam groups.
This meta-analysis provides evidence that ertapenem 1 g once a day can be used as effectively and safely as recommended dose of piperacillin/tazobactam, for the treatment of complicated infections, particularly of mild to moderate severity. It is an appealing option for the treatment of these complicated infections.
厄他培南是一种新的碳青霉烯类抗生素,具有良好的药代动力学特性,已被批准用于治疗复杂性腹腔内感染(cIAI)、急性盆腔感染(API)和复杂性皮肤和皮肤结构感染(cSSSI)。本研究旨在比较厄他培南与哌拉西林/他唑巴坦的疗效和安全性,后者已被报道对这些复杂感染具有良好的疗效。
我们对在 PubMed、Cochrane 图书馆和 Embase 中检索到的比较厄他培南与哌拉西林/他唑巴坦治疗复杂性感染(包括 cIAI、API、cSSSI)的随机对照试验进行了荟萃分析。主要疗效终点是在治愈期评估的临床治疗成功率。主要安全性终点是治疗和治疗后期间发生的与药物相关的临床和实验室不良事件。
纳入了 6 项 RCT,共 3161 例患者,我们的荟萃分析结果显示,厄他培南与哌拉西林/他唑巴坦治疗复杂感染的临床治疗成功率相似(临床可评估人群,1937 例患者,优势比:1.15,95%置信区间:0.89-1.49;意向治疗人群,2855 例患者,优势比:1.03,95%置信区间:0.87-1.22)。所有次要疗效终点分析均获得了与临床治疗成功率相似的结果。厄他培南组与哌拉西林/他唑巴坦组之间药物相关不良事件的发生率无差异。
本荟萃分析提供了证据,表明厄他培南 1 g 每日 1 次可与推荐剂量的哌拉西林/他唑巴坦一样有效和安全地用于治疗复杂性感染,特别是轻至中度感染。对于这些复杂感染的治疗,它是一种有吸引力的选择。