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肺炎链球菌肉汤微量稀释法和纸片扩散法抗菌药物敏感性试验的解释标准及质量控制限度的制定

Development of interpretive criteria and quality control limits for broth microdilution and disk diffusion antimicrobial susceptibility testing of Streptococcus pneumoniae.

作者信息

Jorgensen J H, Swenson J M, Tenover F C, Ferraro M J, Hindler J A, Murray P R

机构信息

Department of Pathology, University of Texas Health Science Center, San Antonio 78284-7750.

出版信息

J Clin Microbiol. 1994 Oct;32(10):2448-59. doi: 10.1128/jcm.32.10.2448-2459.1994.

DOI:10.1128/jcm.32.10.2448-2459.1994
PMID:7814481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC264082/
Abstract

A five-center collaborative study was undertaken to develop quality control and specific interpretive criteria for susceptibility testing of Streptococcus pneumoniae against 12 antimicrobial agents. MICs were determined for 248 pneumococcal clinical isolates (with an emphasis on resistant strains) by use of the National Committee for Clinical Laboratory Standards (NCCLS)-recommended broth microdilution procedure incorporating lysed horse blood-supplemented Mueller-Hinton broth. NCCLS disk diffusion testing was also performed for each isolate by using Mueller-Hinton sheep blood agar incubated in 5% CO2. Repetitive testing of S. pneumoniae ATCC 49619 with different sources and lots of media and disks allowed development of quality control ranges which encompassed approximately 95% of MIC and zone size values observed in the study. Good intra- and interlaboratory reproducibilities were seen with these testing methods and all of the drugs examined. On the basis of the results of this study, MIC interpretive criteria are proposed for 11 agents. Comparisons of MICs and disk diffusion zone sizes allowed disk diffusion zone size interpretive criteria to be proposed for five drugs and confirmed the use of the oxacillin disk test for prediction of penicillin susceptibility among pneumococci. Excessive numbers of minor-category interpretive errors precludes recommendation at this time of the disk diffusion method for testing of pneumococci against five of the drugs. Use of these proposed quality control and interpretive criteria should provide for reproducible test results and allow recognition of recently emerging resistance among pneumococcal clinical isolates.

摘要

开展了一项五中心合作研究,以制定肺炎链球菌对12种抗菌药物药敏试验的质量控制和具体解释标准。使用美国国家临床实验室标准委员会(NCCLS)推荐的肉汤微量稀释程序,在添加了溶解马血的Mueller-Hinton肉汤中,对248株肺炎链球菌临床分离株(重点是耐药菌株)测定了最低抑菌浓度(MIC)。还对每株分离株进行了NCCLS纸片扩散试验,使用在5%二氧化碳环境中孵育的Mueller-Hinton羊血琼脂。对不同来源和批次的培养基及纸片,用肺炎链球菌ATCC 49619进行重复试验,从而确定了质量控制范围,该范围涵盖了研究中观察到的约95%的MIC和抑菌圈大小值。这些检测方法和所有检测的药物在实验室内和实验室间都具有良好的重复性。基于本研究结果,针对11种药物提出了MIC解释标准。通过比较MIC和纸片扩散抑菌圈大小,针对5种药物提出了纸片扩散抑菌圈大小解释标准,并证实了用苯唑西林纸片试验预测肺炎链球菌对青霉素的敏感性。由于小类解释错误数量过多,目前不推荐使用纸片扩散法检测肺炎链球菌对其中5种药物的敏感性。使用这些提议的质量控制和解释标准应能提供可重复的检测结果,并有助于识别肺炎链球菌临床分离株中最近出现的耐药性。

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