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头孢地尔检测的问题:在缺铁培养基中比较商业方法与肉汤微量稀释法——根据欧洲药敏试验委员会初始和修订的解释标准对性能、抗菌单位和拖尾效应的分析

Issues with Cefiderocol Testing: Comparing Commercial Methods to Broth Microdilution in Iron-Depleted Medium-Analyses of the Performances, ATU, and Trailing Effect According to EUCAST Initial and Revised Interpretation Criteria.

作者信息

Stracquadanio Stefano, Nicolosi Alice, Marino Andrea, Calvo Maddalena, Stefani Stefania

机构信息

Department of Biomedical and Biotechnological Sciences, University of Catania, 95123 Catania, Italy.

Unit of Infectious Diseases, Department of Clinical and Experimental Medicine, ARNAS Garibaldi Hospital, University of Catania, 95123 Catania, Italy.

出版信息

Diagnostics (Basel). 2024 Oct 18;14(20):2318. doi: 10.3390/diagnostics14202318.

DOI:10.3390/diagnostics14202318
PMID:39451641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11506871/
Abstract

BACKGROUND

The rise of multi-drug-resistant Gram-negative bacteria necessitates the development of new antimicrobial agents. Cefiderocol shows promising activity by exploiting bacterial iron transport systems to penetrate the outer membranes of resistant pathogens.

OBJECTIVES

This study evaluates the efficacy of cefiderocol testing methods and trailing effect impact using a ComASP Cefiderocol panel, disk diffusion (DD), and MIC test strips (MTS) compared to iron-depleted broth microdilution (ID-BMD).

METHODS

A total of 131 Gram-negative strains from clinical samples was tested by commercial methods and the gold standard. Results were interpreted as per 2024 and 2023 EUCAST guidelines.

RESULTS

ID-BMD revealed high cefiderocol susceptibility among Enterobacterales and , with one isolate being resistant. exhibited higher MIC values, particularly considering trailing effects that complicated MIC readings. ComASP showed 97% categorical agreement (CA) and 66% essential agreement (EA) with ID-BMD for Enterobacterales but failed to detect the resistant . DD tests demonstrated variable CA (72% or 93%), and 38% or 34% of strains within the ATU according to EUCAST Breakpoint Tables v13.0 and 14.0, respectively, with major errors only. MTS for had 100% CA but 44% EA, and often underestimated MIC values.

CONCLUSIONS

The study emphasizes the need for standardized criteria to address trailing effects and ATU and highlights the discrepancies between testing methods. While cefiderocol resistance remains rare, accurate susceptibility testing is crucial for its effective clinical use. The findings suggest that current commercial tests have limitations, necessitating careful interpretation and potential supplementary testing to guide appropriate antibiotic therapy.

摘要

背景

多重耐药革兰氏阴性菌的出现使得开发新型抗菌药物成为必要。头孢地尔通过利用细菌铁转运系统穿透耐药病原体的外膜,显示出有前景的活性。

目的

本研究使用ComASP头孢地尔检测板、纸片扩散法(DD)和MIC测试条(MTS),与缺铁肉汤微量稀释法(ID-BMD)相比,评估头孢地尔检测方法的有效性以及拖尾效应的影响。

方法

通过商业方法和金标准对总共131株来自临床样本的革兰氏阴性菌株进行检测。结果根据2024年和2023年欧洲抗菌药物敏感性试验委员会(EUCAST)指南进行解释。

结果

ID-BMD显示肠杆菌科细菌和 对头孢地尔高度敏感,仅有1株分离株耐药。 显示出较高的MIC值,特别是考虑到拖尾效应使MIC读数变得复杂。对于肠杆菌科细菌,ComASP与ID-BMD的分类一致性(CA)为97%,基本一致性(EA)为66%,但未能检测出耐药的 。DD试验显示CA值变化(分别为72%或93%),根据EUCAST断点表v13.0和14.0,ATU内分别有38%或34%的菌株,且仅有主要错误。针对 的MTS的CA为100%,但EA为44%,并且常常低估MIC值。

结论

该研究强调需要标准化标准来解决拖尾效应和ATU问题,并突出了检测方法之间的差异。虽然头孢地尔耐药性仍然罕见,但准确的药敏试验对于其有效的临床应用至关重要。研究结果表明,当前的商业检测存在局限性,需要谨慎解释并可能进行补充检测以指导适当的抗生素治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b2/11506871/d9f616652a3b/diagnostics-14-02318-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b2/11506871/e4fc7dc57f95/diagnostics-14-02318-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b2/11506871/38f279bf7013/diagnostics-14-02318-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b2/11506871/aa04e67a4297/diagnostics-14-02318-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b2/11506871/fdfe8954ec9b/diagnostics-14-02318-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b2/11506871/d9f616652a3b/diagnostics-14-02318-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b2/11506871/e4fc7dc57f95/diagnostics-14-02318-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b2/11506871/38f279bf7013/diagnostics-14-02318-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b2/11506871/aa04e67a4297/diagnostics-14-02318-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b2/11506871/fdfe8954ec9b/diagnostics-14-02318-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49b2/11506871/d9f616652a3b/diagnostics-14-02318-g005.jpg

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