Juan Antonio Castillo-Polo, Marta Hernández-García, Ainhize Maruri-Aransolo, María-Isabel Morosini, Patricia Ruiz-Garbajosa, Rafael Cantón
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MIC devices evaluation was performed following ISO 20776-2:2021, calculating essential agreement (EA) and bias. DD results were evaluated following 2023 and 2024-EUCAST-guidelines, calculating major errors (ME) and very major errors. Categorical agreement (CA) was determined for all the methods.</p><p><strong>Results: </strong>Overall, EUMDROXF® and ComASP® showed 81.7% (95% CI = 72.9-88.6) and 88.5% (95% CI = 80.8-93.9) EA, +2.6% and +27.9% bias and 99.0% (95% CI = 94.7-99.9) and 98.1% (95% CI = 93.3-99.8) CA, respectively. Liofilchem MIC-gradient strips exhibited 47.1% (95% CI = 37.2-57.1) EA, +2.9% bias and 93.3% (95% CI = 86.7-97.3) CA. In DD, variability between manufacturers was elevated. CA lowered and ME increased more than 10% with 2024-EUCAST-breakpoints modification.</p><p><strong>Conclusions: </strong>DD performance was insufficient to assess FDC resistance in K. pneumoniae and modification of EUCAST-breakpoints did not solve the problem. ComASP® panel fulfilled ISO criteria and could be used as MIC-confirmatory method, at least in K. pneumoniae. However, EUMDROXF®, even close, did not fulfil the EA criterion. 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Here, we evaluated the performance of different FDC testing methods on Klebsiella pneumoniae isolates around this range.</p><p><strong>Methods: </strong>A challenging collection of 104 K. pneumoniae isolates with different FDC susceptibility was designed, including high representation (70%) of the 2024-ATU (21-23 mm) ± 1 mm. MICs were determined by broth-microdilution (BMD) reference method, commercial BMD (ComASP®, EUMDROXF®), MIC-gradient strips (Liofilchem) and disk-diffusion (DD) (Liofilchem, ThermoFisher). MIC devices evaluation was performed following ISO 20776-2:2021, calculating essential agreement (EA) and bias. DD results were evaluated following 2023 and 2024-EUCAST-guidelines, calculating major errors (ME) and very major errors. 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引用次数: 0
摘要
目的:FDC药敏试验具有挑战性,因为没有一种商业试验已被证明能够准确确定技术不确定区域(ATU)的药敏。在此,我们评估了不同FDC检测方法在该范围内对肺炎克雷伯菌分离株的性能。方法:设计了具有不同FDC敏感性的104株肺炎克雷伯菌,其中2024-ATU (21-23 mm)±1 mm的代表性高(70%)。mic采用微液稀释(BMD)参比法、商用BMD (ComASP®、EUMDROXF®)、mic梯度试纸(Liofilchem)和disk-diffusion (DD) (Liofilchem、ThermoFisher)测定。MIC设备评估按照ISO 20776-2:2021进行,计算基本一致性(EA)和偏差。DD结果按照2023和2024- eucast指南进行评估,计算主要误差(ME)和非常主要误差。所有方法均确定了绝对一致(CA)。结果:总体而言,EUMDROXF®和ComASP®的EA分别为81.7% (95% CI = 72.9 ~ 88.6)和88.5% (95% CI = 80.8 ~ 93.9),偏倚分别为+2.6%和+27.9%,CA分别为99.0% (95% CI = 94.7 ~ 99.9)和98.1% (95% CI = 93.3 ~ 99.8)。Liofilchem mic梯度条带的EA值为47.1% (95% CI = 37.2-57.1),偏倚为+2.9%,CA值为93.3% (95% CI = 86.7-97.3)。在DD中,制造商之间的可变性升高。2024- eucast断点修改后,CA降低,ME增加10%以上。结论:DD性能不足以评估肺炎克雷伯菌的FDC耐药,修改eucast断点并不能解决问题。ComASP®面板符合ISO标准,至少在肺炎克雷伯菌中可作为mic验证方法。然而,EUMDROXF®即使接近,也没有达到EA标准。mic梯度条带显示出主要的局限性。
Cefiderocol AST in a real-life Klebsiella pneumoniae collection: challenges in the ATU range.
Objectives: FDC susceptibility testing is challenging as none of the commercial tests have been proven to accurately determine the susceptibility in the area of technical uncertainty (ATU). Here, we evaluated the performance of different FDC testing methods on Klebsiella pneumoniae isolates around this range.
Methods: A challenging collection of 104 K. pneumoniae isolates with different FDC susceptibility was designed, including high representation (70%) of the 2024-ATU (21-23 mm) ± 1 mm. MICs were determined by broth-microdilution (BMD) reference method, commercial BMD (ComASP®, EUMDROXF®), MIC-gradient strips (Liofilchem) and disk-diffusion (DD) (Liofilchem, ThermoFisher). MIC devices evaluation was performed following ISO 20776-2:2021, calculating essential agreement (EA) and bias. DD results were evaluated following 2023 and 2024-EUCAST-guidelines, calculating major errors (ME) and very major errors. Categorical agreement (CA) was determined for all the methods.
Results: Overall, EUMDROXF® and ComASP® showed 81.7% (95% CI = 72.9-88.6) and 88.5% (95% CI = 80.8-93.9) EA, +2.6% and +27.9% bias and 99.0% (95% CI = 94.7-99.9) and 98.1% (95% CI = 93.3-99.8) CA, respectively. Liofilchem MIC-gradient strips exhibited 47.1% (95% CI = 37.2-57.1) EA, +2.9% bias and 93.3% (95% CI = 86.7-97.3) CA. In DD, variability between manufacturers was elevated. CA lowered and ME increased more than 10% with 2024-EUCAST-breakpoints modification.
Conclusions: DD performance was insufficient to assess FDC resistance in K. pneumoniae and modification of EUCAST-breakpoints did not solve the problem. ComASP® panel fulfilled ISO criteria and could be used as MIC-confirmatory method, at least in K. pneumoniae. However, EUMDROXF®, even close, did not fulfil the EA criterion. MIC-gradient strips exhibited major limitations.
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.