首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Comparison of Crystal Enteric/Nonfermenter system API 20E system and Vitek AutoMicrobic system for identification of gram-negative bacilli.
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Comparison of Crystal Enteric/Nonfermenter system API 20E system and Vitek AutoMicrobic system for identification of gram-negative bacilli.

机译:比较用于鉴定革兰氏阴性杆菌的Crystal Enteric / Nonfermenter系统API 20E系统和Vitek AutoMicrobic系统。

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摘要

A comparative evaluation of the Crystal Enteric/Nonfermenter system (Crystal; Becton Dickinson, Cockeysville, Md.), API 20E (API; bioMérieux Vitek, Inc., Hazelwood, Mo.), and the Vitek GNI card (Vitek; bioMérieux Vitek) was performed with 512 clinical isolates of gram-negative bacilli, including 381 members of the family Enterobacteriaceae and 131 nonenteric bacilli. With supplemental testing, API, Crystal, and Vitek correctly identified to the genus and species level 505 (98.6%), 489 (95.5%), and 494 (96.5%) of the 512 isolates, respectively. Supplemental testing, as specified by the manufacturer, was required to identify 119 (23.2%), 18 (3.5%), and 5 (1.0%) of the isolates with the three systems, respectively. Of the 381 isolates from the family Enterobacteriaceae, API and Crystal correctly identified 90.3 and 91.6% by 18 to 24 h without supplemental testing, respectively, and Vitek identified 92.4 and 96.1% following 10 and 18 h of incubation, respectively. Of the 131 nonenteric organisms, API and Crystal correctly identified 28.2 and 93.9% by 18 to 24 h without supplemental testing, respectively, and Vitek identified 84.0% by 10 h and 93.9% by 18 h. Errors in identification with each system were infrequent and appeared to be randomly distributed among the genera evaluated. The three systems were comparable in accuracy when either a weighted clinical laboratory profile of organisms or a group of selected isolates in a stress test sample was evaluated (P > 0.05). There were no significant differences between the three systems in their ability to identify either the isolates in the weighted group or those in the stress test (P > 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)
机译:晶体肠溶/非发酵剂系统(水晶;马里兰州科基斯维尔的Becton Dickinson),API 20E(API;密苏里州黑泽尔伍德的BioMérieuxVitek,Inc.)和Vitek GNI卡(Vitek;bioMérieuxVitek)的比较评估用512株革兰氏阴性细菌的临床分离株进行检测,包括381个肠杆菌科成员和131个非肠杆菌。通过补充测试,API,Crystal和Vitek分别正确识别了512个分离株中的505个(98.6%),489个(95.5%)和494个(96.5%)的水平。按照制造商的规定,需要进行补充测试,以分别鉴定使用这三种系统的119株(23.2%),18株(3.5%)和5株(1.0%)。在没有补充检测的情况下,在18至24小时内,来自肠杆菌科的381株分离物中,API和Crystal分别正确鉴定出90.3和91.6%,在孵育10和18 h后,Vitek分别鉴定出92.4和96.1%。在131种非肠道生物中,未经补充检测的API和Crystal到18至24 h分别正确地鉴定出28.2%和93.9%,Vitek的10 h和18 h时分别鉴定为84.0%和93.9%。每个系统的识别错误很少见,并且似乎在所评估的属中随机分布。当评估压力测试样品中的生物的加权临床实验室概况或一组选定的分离株时,这三个系统的准确性相当(P> 0.05)。三种系统在加权组和压力测试中的分离株识别能力没有显着差异(P> 0.05)(摘要截短为250字)

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