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2012-2016 年头孢他啶/阿维巴坦对肠杆菌科的体外活性的纵向分析。

Longitudinal analysis of the in vitro activity of ceftazidime/avibactam versus Enterobacteriaceae, 2012-2016.

机构信息

Hospital Infante D. Pedro, Av. Universidade, Aveiro 3814-501, Portugal.

Pfizer Inc., Groton, CT, USA.

出版信息

J Glob Antimicrob Resist. 2019 Dec;19:106-115. doi: 10.1016/j.jgar.2019.07.003. Epub 2019 Jul 8.

Abstract

OBJECTIVES

The in vitro activities of ceftazidime/avibactam and comparator antimicrobial agents were analysed against 59 828 Enterobacteriaceae isolates collected by 190 centres from all global regions except North America from 2012-2016 as part of the International Network for Optimal Resistance Monitoring (INFORM) global surveillance programme.

METHODS

Antimicrobial susceptibility testing was performed using Clinical and Laboratory Standards Institute broth microdilution panels at a central reference laboratory, except for isolates collected in China that were tested using frozen, dehydrated broth microdilution panels at a central laboratory in China. The presence of extended-spectrum β-lactamases (ESBLs) was confirmed by multiplex PCR assays.

RESULTS

Ceftazidime/avibactam was the most active agent against all Enterobacteriaceae (MIC, ≤1mg/L, ≥98.4% susceptibility). High rates of susceptibility (>88%) were observed amongst Citrobacter freundii, Citrobacter spp., Enterobacter spp., Escherichia coli, Klebsiella pneumoniae and Klebsiella oxytoca to colistin, meropenem, amikacin and tigecycline. Ceftazidime/avibactam showed consistent in vitro activity against ESBL-positive isolates of E. coli (n=5674; MIC, 0.5mg/L, 99.5% susceptible), K. pneumoniae (n=7097; MIC, 2mg/L, 97.0% susceptible) and K. oxytoca (n = 565; MIC, 1mg/L, 96.8% susceptible). Isolates identified as metallo-β-lactamase-positive (n=242) were not susceptible to ceftazidime/avibactam but were susceptible to tigecycline (76.9%) and colistin (n=194 isolates tested; 92.8%).

CONCLUSIONS

Clinical Enterobacteriaceae isolates, including ESBL-positive phenotypes, collected globally (excluding North America) from 2012-2016 were highly susceptible to ceftazidime/avibactam, suggesting it is a useful agent for serious infections caused by multidrug-resistant organisms belonging to the family Enterobacteriaceae when therapeutic options are limited.

摘要

目的

分析头孢他啶/阿维巴坦和比较抗菌药物对来自全球除北美地区以外的 190 个中心在 2012-2016 年期间收集的 59828 株肠杆菌科细菌的体外活性。

方法

采用临床和实验室标准协会肉汤微量稀释板进行抗菌药物敏感性测试,除中国收集的分离株外,这些分离株在中国的一个中心实验室采用冷冻、脱水肉汤微量稀释板进行测试。通过多重 PCR 检测确认是否存在超广谱β-内酰胺酶(ESBLs)。

结果

头孢他啶/阿维巴坦对所有肠杆菌科细菌(MIC,≤1mg/L,敏感性≥98.4%)最具活性。在弗氏柠檬酸杆菌、柠檬酸杆菌属、肠杆菌属、大肠埃希菌、肺炎克雷伯菌和产酸克雷伯菌中,多黏菌素、美罗培南、阿米卡星和替加环素的敏感性率(>88%)较高。头孢他啶/阿维巴坦对 ESBL 阳性大肠埃希菌(n=5674;MIC,0.5mg/L,99.5%敏感)、肺炎克雷伯菌(n=7097;MIC,2mg/L,97.0%敏感)和产酸克雷伯菌(n=565;MIC,1mg/L,96.8%敏感)的体外活性一致。鉴定为金属β-内酰胺酶阳性(n=242)的分离株对头孢他啶/阿维巴坦无敏感性,但对替加环素(76.9%)和多黏菌素(n=194 株测试;92.8%)敏感。

结论

2012-2016 年期间从全球(不包括北美)收集的临床肠杆菌科细菌,包括 ESBL 阳性表型,对头孢他啶/阿维巴坦高度敏感,表明在治疗选择有限的情况下,当治疗严重的多药耐药菌感染时,头孢他啶/阿维巴坦是一种有用的药物。

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