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BD Phoenix自动化微生物系统用于常见临床分离株鉴定及抗菌药物敏感性试验的评估。

Evaluation of the BD Phoenix Automated Microbiology System for identification and antimicrobial susceptibility testing of common clinical isolates.

作者信息

Liu Z K, Ling T K, Cheng A F

机构信息

Department of Microbiology, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong, China.

出版信息

Med Princ Pract. 2005 Jul-Aug;14(4):250-4. doi: 10.1159/000085744.

Abstract

OBJECTIVE

To evaluate the accuracy and reliability of the BD Phoenix Automated Microbiology System for identification (ID) and antimicrobial susceptibility testing (AST) of Gram-positive and Gram-negative isolates.

MATERIALS AND METHODS

The ID of 291 Gram-negative and 158 Gram-positive clinical isolates were evaluated by the system. The AST of 252 Gram-negative and 151 Gram-positive isolates with correct ID were then evaluated. The results were compared with those of the API ID system and the microbroth dilution method. All discrepant results were repeated for verification.

RESULTS

Over 90% Gram-negative and Gram-positive isolates were correctly identified to species or genus level by the Phoenix system. The minimum inhibitory concentration agreement rates between the Phoenix and the microbroth dilution methods within +/-1 dilution ranged from 87.3 to 97.6% for Gram-negative isolates, and from 50 to 100% for Gram-positive isolates. For Gram-positive isolates, vancomycin had significant low minimum inhibitory concentration agreement rates.

CONCLUSIONS

Overall, the results indicate that the Phoenix system is a reliable system. It could provide accurate ID and AST results for routine clinical laboratories.

摘要

目的

评估BD Phoenix自动化微生物系统对革兰氏阳性和革兰氏阴性分离株进行鉴定(ID)和抗菌药物敏感性试验(AST)的准确性和可靠性。

材料与方法

该系统对291株革兰氏阴性和158株革兰氏阳性临床分离株进行了鉴定。然后对252株革兰氏阴性和151株革兰氏阳性且鉴定正确的分离株进行了抗菌药物敏感性试验。将结果与API ID系统和微量肉汤稀释法的结果进行比较。所有不一致的结果均重复进行验证。

结果

Phoenix系统对90%以上的革兰氏阴性和革兰氏阳性分离株正确鉴定到种或属水平。Phoenix系统与微量肉汤稀释法之间,革兰氏阴性分离株在±1个稀释度内的最低抑菌浓度一致率为87.3%至97.6%,革兰氏阳性分离株为50%至100%。对于革兰氏阳性分离株,万古霉素的最低抑菌浓度一致率显著较低。

结论

总体而言,结果表明Phoenix系统是一个可靠的系统。它可为常规临床实验室提供准确的鉴定和抗菌药物敏感性试验结果。

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