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舒巴坦-哌拉西林药敏纸片的研制、质量控制范围及与分离株 MIC 与纸片结果的相关性。

Sulopenem Disk Development, Quality Control Range, and MIC to Disk Result Correlation for Isolates.

机构信息

Iterum Therapeutics, Old Saybrook, Connecticut, USA.

Laboratory Specialists, Inc., Westlake, Ohio, USA.

出版信息

J Clin Microbiol. 2023 Jul 20;61(7):e0024623. doi: 10.1128/jcm.00246-23. Epub 2023 Jun 26.

Abstract

Sulopenem disk masses of 2, 5, 10, and 20 μg were evaluated by susceptibility testing isolates by broth microdilution and disk diffusion. A 2-μg disk was chosen, and error-rate bounding analysis in accordance with Clinical and Laboratory Standards Institute (CLSI) guideline M23 was conducted using a proposed sulopenem susceptible/intermediate/resistant (S/I/R) interpretive criterion of ≤0.5/1/≥2 μg/mL. Among the evaluated ( = 2,856), very few interpretive errors were observed (no very major errors and only one major error). An eight-laboratory quality control (QC) study was performed using the 2-μg disk, and 99.0% (470/475) of results were within a 7-mm range of 24 to 30 mm. Results were similar by disk lot and media, and no outlier sites were observed. A sulopenem 2-μg disk QC range for Escherichia coli 29522 of 24 to 30 mm was established by the CLSI. A 2-μg sulopenem disk performs accurately and reproducibly for testing of .

摘要

Sulopenem 药敏试验采用肉汤微量稀释法和纸片扩散法对 2、5、10 和 20μg 药敏纸片进行评估。选用 2μg 药敏纸片,参照临床和实验室标准协会(CLSI)M23 指南,用提议的 sulopenem 敏感/中介/耐药(S/I/R)解释标准(≤0.5/1/≥2μg/mL)进行误差界限分析。在所评估的 ( = 2856)中,观察到的解释错误很少(没有非常大的错误,只有一个大的错误)。用 2μg 药敏纸片进行了 8 个实验室质量控制(QC)研究,99.0%(470/475)的结果在 24 到 30mm 的 7mm 范围内。药敏纸片批次和培养基的结果相似,没有观察到异常点。CLSI 建立了大肠埃希菌 29522 的 sulopenem 2μg 药敏纸片 QC 范围为 24 到 30mm。用于检测 的 2μg sulopenem 药敏纸片的准确性和重现性良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acd9/10358168/8efb5f2151cd/jcm.00246-23-f001.jpg

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