Global evaluation of the antibacterial activity of Ceftolozane/Tazobactam against ESBLs-producing Escherichia coli and Klebsiella pneumoniae: a systematic review and meta-analysis.

IF 3.8 Q2 INFECTIOUS DISEASES
Therapeutic Advances in Infectious Disease Pub Date : 2023-11-17 eCollection Date: 2023-01-01 DOI:10.1177/20499361231212074
Marzieh Rahim Khorasani, Soodabeh Rostami, Arash Bakhshi, Raheleh Sheikhi
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引用次数: 0

Abstract

Background: Ceftolozane/Tazobactam is a β-lactam/β-lactamase inhibitor combination with a high range of efficacy and broad-spectrum action against multidrug-resistant bacterial strains.

Objectives: The present study aimed to analyze the in vitro activity of Ceftolozane/Tazobactam against extended-spectrum β-lactamases (ESBLs)-producing Escherichia coli (ESBLs-EC) and Klebsiella pneumonia (ESBLs-KP) in the published literature to provide international data on the antimicrobial stewardship programs.

Design: Systematic review and meta-analysis.

Methods: A systematic literature search was conducted on the Web of Science, Embase, PubMed, Scopus, and Google Scholar electronic databases from the beginning of databases to December 2022 to cover all published articles relevant to our scope.

Results: At last, 31 publications that met our inclusion criteria were selected for data extraction and analysis by Comprehensive Meta-Analysis Software. The pooled prevalence of Ceftolozane/Tazobactam susceptibility for ESBLs-EC and ESBLs-KP was estimated at 91.3% [95% confidence interval (CI): 90.1-92.5%] and 65.6% (95% CI: 60.8-70.2%), respectively. There was significant heterogeneity among the 31 studies for ESBLs-EC (χ2 = 91.621; p < 0.001; I2 = 67.256%) and ESBLs-KP (χ2 = 348.72; p < 0.001; I2 = 91.4%). Most clinical isolates of ESBLs-EC had MIC50 and MIC90 at a concentration of 0.5 and 2 µg/mL [minimum inhibitory concentration (MIC) at which 50% and 90% of isolates were inhibited], respectively. In contrast, most clinical isolates of ESBLs-KP had MIC50 and MIC90 at a concentration of 1 and 32 µg/mL, respectively.

Conclusion: Based on the meta-analysis results, Ceftolozane/Tazobactam has a more promising in vitro antibacterial activity against ESBLs-EC isolates from different clinical sources than ESBLs-KP isolates. Therefore, Ceftolozane/Tazobactam can be a useful therapeutic drug as an alternative to carbapenems. Randomized clinical trials are needed to provide clinical evidence to support these observations.

头孢唑烷/他唑巴坦对产esbls的大肠杆菌和肺炎克雷伯菌抗菌活性的全球评价:系统综述和荟萃分析。
背景:头孢洛桑/他唑巴坦是一种联合β-内酰胺/β-内酰胺酶抑制剂,对多药耐药菌株具有高效域和广谱作用。目的:本研究旨在分析头孢唑烷/他唑巴坦对广谱β-内酰胺酶(ESBLs)产生的大肠杆菌(ESBLs- ec)和肺炎克雷伯菌(ESBLs- kp)的体外活性,为抗菌药物管理计划提供国际数据。设计:系统回顾和荟萃分析。方法:系统检索Web of Science、Embase、PubMed、Scopus、Google Scholar等电子数据库自建库之初至2022年12月的所有与我们研究范围相关的已发表文章。结果:最终选取符合纳入标准的31篇文献,通过综合meta分析软件进行数据提取和分析。ESBLs-EC和ESBLs-KP对头孢唑烷/他唑巴坦的总易感率估计分别为91.3%[95%置信区间(CI): 90.1-92.5%]和65.6% (95% CI: 60.8-70.2%)。31项ESBLs-EC研究间存在显著异质性(χ2 = 91.621;p 2 = 67.256%)和ESBLs-KP (χ2 = 348.72;p I2 = 91.4%)。大多数ESBLs-EC临床分离株在0.5µg/mL和2µg/mL[最低抑制浓度(MIC), 50%和90%的分离株被抑制]时的MIC50和MIC90分别为。相比之下,大多数ESBLs-KP临床分离株的MIC50和MIC90浓度分别为1和32µg/mL。结论:综合meta分析结果,头孢唑烷/他唑巴坦对不同临床来源的ESBLs-EC菌株的体外抗菌活性均优于ESBLs-KP菌株。因此,头孢唑烷/他唑巴坦可以作为碳青霉烯类的一种有用的替代治疗药物。需要随机临床试验来提供临床证据来支持这些观察结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.30
自引率
8.80%
发文量
64
审稿时长
9 weeks
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