Evaluation of the BD Phoenix Automated Microbiology System for identification and antimicrobial susceptibility testing of common clinical isolates
被引:8
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作者:
Liu, ZK
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机构:
Chinese Univ Hong Kong, Prince Wales Hosp, Dept Microbiol, Hong Kong, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Prince Wales Hosp, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
Liu, ZK
[1
]
Ling, TK
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Chinese Univ Hong Kong, Prince Wales Hosp, Dept Microbiol, Hong Kong, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Prince Wales Hosp, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
Ling, TK
[1
]
Cheng, AF
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Chinese Univ Hong Kong, Prince Wales Hosp, Dept Microbiol, Hong Kong, Hong Kong, Peoples R ChinaChinese Univ Hong Kong, Prince Wales Hosp, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
Cheng, AF
[1
]
机构:
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
BD Phoenix Automated Microbiology System;
API system;
microbroth dilution method;
D O I:
10.1159/000085744
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
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 Phonenix and the microbroth dilution methods within 8 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. Copyright (C) 2005 S. Karger AG, Basel.
机构:
Univ Kentucky, Coll Pharm, Lexington, KY USA
Vanderbilt Univ, Med Ctr, 1211 Med Ctr Dr, Nashville, TN USAUniv Kentucky, Coll Pharm, Lexington, KY USA
Haffler, Zachary J.
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机构:
Kulengowski, Brandon
Ribes, Julie A.
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机构:
Univ Kentucky, Albert B Chandler Hosp, Pathol & Lab Med, Lexington, KY USAUniv Kentucky, Coll Pharm, Lexington, KY USA
Ribes, Julie A.
Burgess, David S.
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机构:
Univ Kentucky, Coll Pharm, Dept Pharm Practice & Sci, 789 South Limestone, Lexington, KY 40536 USAUniv Kentucky, Coll Pharm, Lexington, KY USA