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本文引用的文献

1
Detection of extended-spectrum beta-lactamases among Enterobacteriaceae by use of semiautomated microbiology systems and manual detection procedures.使用半自动微生物系统和手工检测程序检测肠杆菌科细菌中的超广谱β-内酰胺酶
J Clin Microbiol. 2007 Apr;45(4):1167-74. doi: 10.1128/JCM.01988-06. Epub 2007 Feb 7.
2
Prevalence of newer beta-lactamases in gram-negative clinical isolates collected in the United States from 2001 to 2002.2001年至2002年在美国收集的革兰氏阴性临床分离株中新型β-内酰胺酶的流行情况。
J Clin Microbiol. 2006 Sep;44(9):3318-24. doi: 10.1128/JCM.00756-06.
3
Evaluation of the new VITEK 2 extended-spectrum beta-lactamase (ESBL) test for rapid detection of ESBL production in Enterobacteriaceae isolates.新型VITEK 2超广谱β-内酰胺酶(ESBL)检测法用于快速检测肠杆菌科分离株中ESBL产生情况的评估。
J Clin Microbiol. 2006 Sep;44(9):3257-62. doi: 10.1128/JCM.00433-06.
4
Extended-spectrum beta-lactamases: a clinical update.超广谱β-内酰胺酶:临床最新进展
Clin Microbiol Rev. 2005 Oct;18(4):657-86. doi: 10.1128/CMR.18.4.657-686.2005.
5
Emergence of KPC-possessing Klebsiella pneumoniae in Brooklyn, New York: epidemiology and recommendations for detection.纽约布鲁克林产肺炎克雷伯菌碳青霉烯酶(KPC)的肺炎克雷伯菌的出现:流行病学及检测建议
Antimicrob Agents Chemother. 2005 Jul;49(7):3018-20. doi: 10.1128/AAC.49.7.3018-3020.2005.
6
Detection of KPC carbapenem-hydrolyzing enzymes in Enterobacter spp. from Brooklyn, New York.纽约布鲁克林地区肠杆菌属中KPC碳青霉烯水解酶的检测。
Antimicrob Agents Chemother. 2005 Feb;49(2):776-8. doi: 10.1128/AAC.49.2.776-778.2005.
7
Outbreak of Klebsiella pneumoniae producing a new carbapenem-hydrolyzing class A beta-lactamase, KPC-3, in a New York Medical Center.纽约一家医疗中心爆发产新型碳青霉烯水解酶A类β-内酰胺酶KPC-3的肺炎克雷伯菌感染。
Antimicrob Agents Chemother. 2004 Dec;48(12):4793-9. doi: 10.1128/AAC.48.12.4793-4799.2004.
8
Emergence of carbapenem-resistant Klebsiella species possessing the class A carbapenem-hydrolyzing KPC-2 and inhibitor-resistant TEM-30 beta-lactamases in New York City.纽约市出现携带A类碳青霉烯水解酶KPC - 2和抑制剂耐药性TEM - 30β-内酰胺酶的耐碳青霉烯克雷伯菌属细菌。
Clin Infect Dis. 2004 Jul 1;39(1):55-60. doi: 10.1086/421495. Epub 2004 Jun 14.
9
Characterization of clinical isolates of Enterobacteriaceae from Italy by the BD Phoenix extended-spectrum beta-lactamase detection method.采用BD Phoenix超广谱β-内酰胺酶检测方法对来自意大利的肠杆菌科临床分离株进行鉴定。
J Clin Microbiol. 2003 Apr;41(4):1463-8. doi: 10.1128/JCM.41.4.1463-1468.2003.
10
Plasmid-mediated, carbapenem-hydrolysing beta-lactamase, KPC-2, in Klebsiella pneumoniae isolates.肺炎克雷伯菌分离株中质粒介导的碳青霉烯水解β-内酰胺酶KPC-2
J Antimicrob Chemother. 2003 Mar;51(3):711-4. doi: 10.1093/jac/dkg124.

用于分析具有明确特征β-内酰胺酶的大肠杆菌和克雷伯菌分离株的Phoenix和VITEK 2超广谱β-内酰胺酶检测试验的比较

Comparison of Phoenix and VITEK 2 extended-spectrum-beta-lactamase detection tests for analysis of Escherichia coli and Klebsiella isolates with well-characterized beta-lactamases.

作者信息

Thomson Kenneth S, Cornish Nancy E, Hong Seong G, Hemrick Kim, Herdt Christian, Moland Ellen S

机构信息

Department of Medical Microbiology and Immunology, Creighton University School of Medicine, Omaha, Nebraska 68178, USA.

出版信息

J Clin Microbiol. 2007 Aug;45(8):2380-4. doi: 10.1128/JCM.00776-07. Epub 2007 Jun 27.

DOI:10.1128/JCM.00776-07
PMID:17596369
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1951213/
Abstract

The VITEK 2 and Phoenix extended-spectrum beta-lactamase (ESBL) detection systems, which comprise confirmatory tests and expert systems, were evaluated for their ability to discriminate between 102 well-characterized strains of ESBL-positive or -negative Escherichia coli, Klebsiella pneumoniae, and Klebsiella oxytoca. At least 38 distinct ESBLs were included. The strains were chosen to include some known to cause false-positive and false-negative CLSI ESBL confirmatory test results. Therefore, enzyme characterizations, rather than CLSI tests, were the reference methods for the Phoenix and VITEK 2 evaluations. A third arm of the study was conducted with the Phoenix test using two normally inactive expert rules intended to enhance ESBL detection, in addition to using the currently available software. The Phoenix ESBL confirmatory test and unmodified expert system exhibited 96% sensitivity and 81% specificity for ESBL detection. Activation of the two additional rules increased sensitivity to 99% but reduced the specificity to 58%. The VITEK 2 ESBL confirmatory test exhibited 91% sensitivity, which was reduced to 89% sensitivity by its expert system, while its specificity was 85%. Many of the expert system interpretations of both instruments were helpful, but some were suboptimal. The VITEK 2 expert system was potentially more frustrating because it provided more inconclusive interpretations of the results. Considering the high degree of diagnostic difficulty posed by the strains, both ESBL confirmatory tests were highly sensitive. The expert systems of both instruments require modification to update and enhance their utility.

摘要

对VITEK 2和Phoenix超广谱β-内酰胺酶(ESBL)检测系统进行了评估,这两个系统包括确证试验和专家系统,用于鉴别102株特征明确的ESBL阳性或阴性大肠杆菌、肺炎克雷伯菌和产酸克雷伯菌。其中至少包括38种不同的ESBL。选择这些菌株是为了纳入一些已知会导致CLSI ESBL确证试验出现假阳性和假阴性结果的菌株。因此,酶特性鉴定而非CLSI试验是Phoenix和VITEK 2评估的参考方法。该研究的第三个分支使用Phoenix试验,除了使用现有的软件外,还使用了两条通常不活跃的专家规则来增强ESBL检测。Phoenix ESBL确证试验和未修改的专家系统在ESBL检测中表现出96%的灵敏度和81%的特异性。激活另外两条规则可将灵敏度提高到99%,但特异性降至58%。VITEK 2 ESBL确证试验的灵敏度为91%,其专家系统将灵敏度降至89%,而其特异性为85%。两种仪器的专家系统对许多结果的解释都有帮助,但有些并不理想。VITEK 2专家系统可能更令人沮丧,因为它对结果提供了更多不确定的解释。考虑到这些菌株带来的高度诊断困难,两种ESBL确证试验都具有很高的灵敏度。两种仪器的专家系统都需要改进,以更新和增强其效用。