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氨曲南与阿维巴坦联合用于产NDM菌株的抗菌药物敏感性试验:采用CLSI和EUCAST方法的比较评估

Antimicrobial Susceptibility Testing of the Combination of Aztreonam and Avibactam in NDM-Producing : A Comparative Evaluation Using the CLSI and EUCAST Methods.

作者信息

Chan Linda Mei-Wah, Lok Doris Yui Ling, Wong River Chun Wai, Lee Alfred Lok-Hang, Cheung Ingrid Yu-Ying, Lai Christopher Koon-Chi, Chow Viola C Y

机构信息

Department of Microbiology, Prince of Wales Hospital, Sha Tin, New Territories, Hong Kong SAR, China.

Department of Microbiology, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.

出版信息

Antibiotics (Basel). 2025 Jul 3;14(7):675. doi: 10.3390/antibiotics14070675.

Abstract

: The combination of aztreonam (ATM) and avibactam (AVI) presents an important therapeutic option for carbapenem-resistant , particularly the NDM-producing . In 2024, both the CLSI and EUCAST published their methods in antimicrobial susceptibility testing for this combination of agents. : Forty carbapenem-resistant isolates, including ( = 35), complex ( = 2), complex ( = 2), and complex ( = 1) were included in this study. All isolates harbored the NDM carbapenemase except one, which had no known detected carbapenemases. Four antimicrobial susceptibility testing methods of the combination of ATM and AVI were evaluated on these isolates, including the CLSI broth disk elution (BDE) method, the disk diffusion (DD) method of aztreonam-avibactam (AZA) following the EUCAST breakpoints, the MIC test strip (MTS) method of AZA following the EUCAST breakpoints, and the gradient strip stacking (SS) method. BDE was used as the standard of comparison. : Using BDE as the standard of comparison, the AZA DD, AZA MTS, and SS methods had 100% categorical agreement (CA), 0% very major error (VME), and 0% major error (ME). The essential agreement (EA) between the AZA MTS and SS method was 57.5%. : The AZA DD, AZA MTS, and the SS methods showed complete concordance with the BDE method. However, the MICs obtained from the AZA MTS and SS were not comparable.

摘要

氨曲南(ATM)和阿维巴坦(AVI)联合使用为耐碳青霉烯类细菌,尤其是产NDM的细菌提供了一种重要的治疗选择。2024年,临床和实验室标准协会(CLSI)和欧洲抗菌药物敏感性试验委员会(EUCAST)都公布了针对这种联合用药的抗菌药物敏感性试验方法。本研究纳入了40株耐碳青霉烯类细菌分离株,包括大肠埃希菌(n = 35)、克雷伯菌属复合体(n = 2)、肠杆菌属复合体(n = 2)和沙雷菌属复合体(n = 1)。除1株未检测到已知碳青霉烯酶的分离株外,所有分离株均携带NDM碳青霉烯酶。对这些分离株评估了ATM与AVI联合使用的四种抗菌药物敏感性试验方法,包括CLSI肉汤纸片洗脱(BDE)法、遵循EUCAST折点的氨曲南-阿维巴坦(AZA)纸片扩散(DD)法、遵循EUCAST折点的AZA MIC试验条(MTS)法和梯度条叠加(SS)法。以BDE法作为比较标准。以BDE法作为比较标准,AZA DD法、AZA MTS法和SS法的分类一致性(CA)为100%,极重大误差(VME)为0%,重大误差(ME)为0%。AZA MTS法和SS法之间的基本一致性(EA)为57.5%。AZA DD法、AZA MTS法和SS法与BDE法显示完全一致。然而,从AZA MTS法和SS法获得的MIC不可比。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7660/12291778/88164f017042/antibiotics-14-00675-g001.jpg

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