In vitro activity of imipenem/relebactam and ceftazidime/avibactam against carbapenem-resistant Klebsiella pneumoniae from blood cultures in a University hospital in Serbia.

IF 1.3 4区 医学 Q4 IMMUNOLOGY
Acta microbiologica et immunologica Hungarica Pub Date : 2023-08-03 Print Date: 2023-09-21 DOI:10.1556/030.2023.02108
Sanja Zornic, Ivana Petrovic, Bojana Lukovic
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引用次数: 1

Abstract

The study aimed to investigate prevalence of carbapenem-resistant Klebsiella pneumoniae (CRKP) blood culture isolates and their susceptibility to two new antibiotics, imipenem/relebactam and ceftazidime/avibactam. Out of 765 isolates recovered from blood cultures in a tertiary care hospital in Serbia between 2020 and 2023, 143 non-repetitive K. pneumoniae strains were included in this study. Minimum inhibitory concentration (MIC) values of the examined antimicrobial drugs was determined by VITEK 2 system, MIC test strip (imipenem/relebactam and ceftazidime/avibactam), and broth microdilution method (tigecycline and colistin). Carbapenemase-encoding genes (blaKPC, blaOXA-48-like, blaNDM, blaVIM, blaIMP) were detected using a multiplex-PCR assay, the BioFire-Blood Culture Identification 2-panel. This closed molecular assay is designed for the BioFire® FilmArray® system, enabling automated sample preparation, amplification, detection, and analysis (bioMérieux, France). Results revealed that K. pneumoniae was the most common isolate from blood cultures in 2022. The prevalence of K. pneumoniae was about 11.6% in 2020 and 2021, while in 2022 it raised to over 30%. Also, the frequency of CRKP increased from 11.76% in 2020, through 15.29% in 2021 to 72.94% in 2022. The majority of CRKP carried blaOXA-48-like (60.0%), followed by blaKPC (16.47%), and blaNDM (8.24%) genes, while 14.12% harboured both blaOXA-48-like and blaNDM genes. Only 25.88% of CRKP isolates were resistant to ceftazidime/avibactam, while 51.76% were resistant to imipenem/relebactam and colistin. The rapid spread of CRKP is particularly concerning because therapeutic options are limited to a few antibiotics. While imipenem/relebactam and colistin showed similar antimicrobial activity against CRKP clinical isolates, ceftazidime/avibactam proved to be the most effective antibiotic.

在塞尔维亚一所大学医院的血液培养中,亚胺培南/雷巴坦和头孢他啶/阿维巴坦对碳青霉烯耐药性肺炎克雷伯菌的体外活性。
本研究旨在调查耐碳青霉烯肺炎克雷伯菌(CRKP)血液培养分离株的流行率及其对两种新抗生素亚胺培南/雷巴坦和头孢他啶/阿维巴坦的易感性。2020年至2023年间,在塞尔维亚一家三级护理医院从血液培养中回收的765株分离株中,143株非重复性肺炎克雷伯菌被纳入本研究。用VITEK-2系统、MIC试纸条(亚胺培南/雷巴坦和头孢他啶/阿维巴坦)和肉汤微量稀释法(替加环素和粘菌素)测定受试抗菌药物的最小抑菌浓度(MIC)值。碳青霉烯酶编码基因(blaKPC、blaOXA-48-样、blaNDM、blaVIM、blaIMP)使用多重PCR检测,即BioFire血液培养鉴定2-面板进行检测。这种封闭分子分析是为BioFire®FilmArray®系统设计的,能够实现自动化的样品制备、扩增、检测和分析(bioMérieux,法国)。结果显示,肺炎克雷伯菌是2022年血液培养中最常见的分离株。肺炎克雷伯菌的患病率在2020年和2021年约为11.6%,而在2022年上升到30%以上。此外,CRKP的频率从2020年的11.76%、2021年的15.29%增加到2022年的72.94%。大多数CRKP携带blaOXA-48样基因(60.0%),其次是blaKPC(16.47%)和blaNDM(8.24%),而14.12%同时携带blaOXA-48样和blaNDM基因。只有25.88%的CRKP分离株对头孢他啶/阿维巴坦具有耐药性,而51.76%的分离株对亚胺培南/雷巴坦和粘菌素具有耐药性。CRKP的快速传播尤其令人担忧,因为治疗选择仅限于几种抗生素。亚胺培南/雷巴坦和粘菌素对CRKP临床分离株显示出相似的抗菌活性,而头孢他啶/阿维巴坦被证明是最有效的抗生素。
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
2.30
自引率
13.30%
发文量
36
审稿时长
>12 weeks
期刊介绍: AMIH is devoted to the publication of research in all fields of medical microbiology (bacteriology, virology, parasitology, mycology); immunology of infectious diseases and study of the microbiome related to human diseases.
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