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Evaluation of the Blue-Carba test for rapid detection of carbapenemases in gram-negative bacilli.评估Blue-Carba试验用于快速检测革兰氏阴性杆菌中的碳青霉烯酶。
J Clin Microbiol. 2015 Jun;53(6):1996-8. doi: 10.1128/JCM.03026-14. Epub 2015 Mar 25.
3
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CarbAcineto NP test for rapid detection of carbapenemase-producing Acinetobacter spp.用于快速检测产碳青霉烯酶不动杆菌属的CarbAcineto NP试验
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Isolation of NDM-producing Providencia rettgeri in Brazil.在巴西分离出产新德里金属β-内酰胺酶的雷氏普罗威登斯菌。
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J Clin Microbiol. 2013 Sep;51(9):3097-101. doi: 10.1128/JCM.00965-13. Epub 2013 Jul 3.
7
Evaluation of the Carba NP test for rapid detection of carbapenemase-producing Enterobacteriaceae and Pseudomonas aeruginosa.碳青霉烯酶快速检测试验(Carba NP 试验)用于检测产碳青霉烯酶肠杆菌科细菌和铜绿假单胞菌的评价。
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Isolation of genetically unrelated bla(NDM-1)-positive Providencia rettgeri strains in Israel.在以色列分离出基因不相关的bla(NDM - 1)阳性雷氏普罗威登斯菌菌株。
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Rapid detection of carbapenemase-producing Enterobacteriaceae.产碳青霉烯酶肠杆菌科的快速检测。
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用于直接从细菌培养物中增强检测碳青霉烯酶产生菌的简化Carba NP试验方案

Simplified Protocol for Carba NP Test for Enhanced Detection of Carbapenemase Producers Directly from Bacterial Cultures.

作者信息

Pasteran Fernando, Tijet Nathalie, Melano Roberto G, Corso Alejandra

机构信息

Servicio Antimicrobianos, Laboratorio Nacional y Regional de Referencia en Antimicrobianos, Instituto Nacional de Enfermedades Infecciosas (INEI), ANLIS Dr. Carlos G. Malbrán, Ministerio de Salud de la Nación, Buenos Aires, Argentina.

Public Health Ontario Laboratories (PHOL), Toronto, Ontario, Canada.

出版信息

J Clin Microbiol. 2015 Dec;53(12):3908-11. doi: 10.1128/JCM.02032-15. Epub 2015 Sep 30.

DOI:10.1128/JCM.02032-15
PMID:26424841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4652111/
Abstract

We compared carbapenemase detection among 266 Gram-negative bacilli (161 carbapenemase producers) using the Carba NP tests issued by the CLSI (CNPt-CLSI) and a novel protocol (CNPt-direct) designed for carbapenemase detection direct from bacterial cultures (instead of bacterial extracts required by the CLSI tests). The specificities were comparable (100%), but the CNPt-direct was more sensitive (98% versus 84%). The CNPt-direct was easier to perform due to the direct use of colonies and offered a more robust detection of carbapenemase producers.

摘要

我们使用美国临床和实验室标准协会(CLSI)发布的碳青霉烯酶检测方法(CNPt-CLSI)和一种专为直接从细菌培养物中检测碳青霉烯酶而设计的新方法(CNPt-direct,而非CLSI检测方法所要求的细菌提取物),对266株革兰氏阴性杆菌(161株碳青霉烯酶产生菌)进行了碳青霉烯酶检测比较。两种方法的特异性相当(均为100%),但CNPt-direct更敏感(98%对84%)。由于直接使用菌落,CNPt-direct操作更简便,且对碳青霉烯酶产生菌的检测更可靠。