Multicenter Evaluation of the New Etest Gradient Diffusion Method for Piperacillin-Tazobactam Susceptibility Testing of Enterobacterales, Pseudomonas aeruginosa, and Acinetobacter baumannii Complex

被引:19
|
作者
Garcia-Fernandez, Sergio [1 ,2 ,8 ]
Bala, Yohann [3 ]
Armstrong, Tom [4 ]
Garcia-Castillo, Maria [1 ,2 ,8 ]
Burnham, Carey-Ann D. [5 ]
Wallace, Meghan A. [5 ]
Hardy, Dwight [6 ]
Zambardi, Gilles [7 ]
Canton, Rafael [1 ,2 ,8 ]
机构
[1] Hosp Univ Ramon & Cajal, Serv Microbiol, Madrid, Spain
[2] IRYCIS, Madrid, Spain
[3] BioMerieux Global Clin Affairs, Marcy Letoile, France
[4] BioMerieux Global Clin Affairs, Hazelwood, MO USA
[5] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[6] Univ Rochester, Med Ctr, Rochester, NY 14642 USA
[7] BioMerieux, La Balme Les Grottes, France
[8] REIPI, Madrid, Spain
关键词
piperacillin-tazobactam; Etest; antimicrobial susceptibility testing; gradient diffusion; Enterobacterales; Pseudomonas aeruginosa; Acinetobacter baumannii complex; ESCHERICHIA-COLI; LACTAMASE;
D O I
10.1128/JCM.01042-19
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Piperacillin-tazobactam (P/T) is a beta-lactam-beta-lactamase inhibitor combination frequently used in the hospital setting. Etest is a gradient diffusion method that represents an alternative to broth microdilution (BMD) for performing antimicrobial susceptibility testing. We conducted a multicenter evaluation of the performance of the new P/T Etest compared to that of BMD following U.S. Food and Drug Administration (FDA) and International Standards Organization (ISO) standard ISO 20776-2 criteria using Clinical and Laboratory Standards Institute (CLSI)-FDA and European Committee on Antimicrobial Susceptibility Testing (EUCAST) interpretive breakpoints, respectively. A total of 977 isolates (775 Enterobacterales isolates, 119 Pseudomonas aeruginosa isolates, and 83 Acinetobacter baumannii complex isolates) were tested. Overall essential agreement (EA) was 96.4% and 96.6% for Enterobacterales when FDA and ISO 20776-2 criteria, respectively, were followed. EA was 98.3% for P. aeruginosa and 91.6% for the A. baumannii complex when both the FDA and ISO criteria were followed. Applying CLSI-FDA breakpoints, categorical agreement (CA) reached 93.0%, 93.3%, and 89.2% for the Enterobacterales, P. aeruginosa, and the A. baumannii complex, respectively. Two very major errors (VMEs; 1.1%) were found among the Enterobacterales (for 2 Klebsiella pneumoniae isolates). No additional major errors (MEs) or VMEs were found. Applying EUCAST breakpoints, CA was 94.8% and 95.8% for Enterobacterales and P. aeruginosa, respectively (no breakpoints are currently available for the A. baumannii complex). No VMEs were observed among the Enterobacterales, but 2 (0.4%) MEs were found. Among the P. aeruginosa isolates, 2 (6.9%) VMEs and 3 (33%) MEs were observed. These errors resulted when P/T Etest MICs were 1 doubling dilution apart from the BMD MICs. In conclusion, the new P/T Etest represents an accurate tool for performing antimicrobial susceptibility testing of Enterobacterales, P. aeruginosa, and A. baumannii complex isolates with limited category errors.
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页数:9
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