Comparative evaluation of disc diffusion and Liofilchem™ MTS strip methods with broth microdilution for cefepime/enmetazobactam susceptibility testing.

IF 3.6 2区 医学 Q1 INFECTIOUS DISEASES Journal of Antimicrobial Chemotherapy Pub Date : 2025-05-02 DOI:10.1093/jac/dkaf051
Cécile Emeraud, Hippolyte De Swardt, Sandrine Bernabeu, Lena Latour, Alice Pages, Sarah Ronsin, Rémy A Bonnin, Laurent Dortet
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Abstract

Background: Cefepime/enmetazobactam is a newly approved β-lactam/β-lactamase inhibitor combination with promising activity against MDR Gram-negative Enterobacterales, particularly ESBL- and OXA-48-producing isolates. Reliable susceptibility testing methods are essential to guide its clinical use.

Objectives: To evaluate the performance of two commercial cefepime/enmetazobactam susceptibility testing methods, disc diffusion and Liofilchem™ MTS gradient strips, using broth microdilution (BMD) as the gold standard.

Methods: A total of 291 carbapenem-resistant Enterobacterales isolates, including 194 carbapenemase producers, were included. Susceptibility testing was performed using BMD, disc diffusion and Liofilchem™ MTS strips. Results were interpreted following EUCAST and FDA 2025 breakpoints. Essential agreement (EA) and bias were calculated for gradient strip methods according to the ISO 20776-2021 guideline, whereas categorical agreement (CA), very major errors (VMEs) and major errors (MEs) were determined for disc diffusion according to the ISO 20776-2:2007 guideline.

Results: The disc diffusion method demonstrated high CA (93.8% EUCAST, 95.9% FDA). VME rates exceeded acceptable thresholds using EUCAST breakpoints (20.8%) but were within limits for FDA (1.9%). Liofilchem™ MTS strips achieved 88.3% (95% CI: 84.1%-91.5%) EA and a bias of -8.9%. Both methods accurately detected susceptibility in OXA-48-producing isolates but showed limitations for isolates close to the MIC breakpoints.

Conclusions: Disc diffusion and Liofilchem™ MTS strips represent reliable alternatives to BMD for routine cefepime/enmetazobactam testing.

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盘片扩散法与微量肉汤稀释Liofilchem™MTS试纸法对头孢吡肟/恩美唑巴坦药敏试验的比较评价
背景:Cefepime/enmetazobactam是一种新批准的β-内酰胺/β-内酰胺酶抑制剂组合,对耐多药革兰氏阴性肠杆菌,特别是产生ESBL和oxa -48的分离菌具有良好的活性。可靠的药敏试验方法对指导其临床应用至关重要。目的:以微量肉汤稀释(BMD)为金标准,评价两种市售头孢吡肟/恩美他唑巴坦药敏试验方法:圆盘扩散法和Liofilchem™MTS梯度试纸条的性能。方法:共收集耐碳青霉烯类肠杆菌291株,其中碳青霉烯酶产生菌194株。药敏试验采用BMD、椎间盘弥散和Liofilchem™MTS试纸进行。结果按照EUCAST和FDA 2025断点进行解释。根据ISO 20776-2021指南计算梯度条法的基本一致性(EA)和偏倚,而根据ISO 20776-2:2007指南确定圆盘扩散法的绝对一致性(CA)、非常大误差(VMEs)和主要误差(MEs)。结果:碟状扩散法具有较高的CA (EUCAST 93.8%, FDA 95.9%)。使用EUCAST断点,VME率超过可接受阈值(20.8%),但在FDA的限制范围内(1.9%)。Liofilchem™MTS试纸的EA为88.3% (95% CI: 84.1%-91.5%),偏倚为-8.9%。两种方法均能准确检测产生oxa -48的分离株的敏感性,但对接近MIC断点的分离株存在局限性。结论:椎间盘弥散和Liofilchem™MTS试纸是常规头孢吡肟/恩美他唑巴坦测试的可靠替代方法。
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来源期刊
CiteScore
9.20
自引率
5.80%
发文量
423
审稿时长
2-4 weeks
期刊介绍: The Journal publishes articles that further knowledge and advance the science and application of antimicrobial chemotherapy with antibiotics and antifungal, antiviral and antiprotozoal agents. The Journal publishes primarily in human medicine, and articles in veterinary medicine likely to have an impact on global health.
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