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1 y of an isolate allows for strain typing and antimicrobial susceptibility testing).
2 phoresis, extended virulence genotyping, and antimicrobial susceptibility testing.
3 demonstrated an added value for LC-MS/MS in antimicrobial susceptibility testing.
4 ria promulgated by the European Committee on Antimicrobial Susceptibility Testing.
5 Antimicrobial susceptibility testing.
6 t bacilli smears, and microbial cultures and antimicrobial susceptibility testing.
7 nating the need for biochemical analysis and antimicrobial susceptibility testing.
8 ime needed for phenotypic identification and antimicrobial susceptibility testing.
9 gel electrophoresis (PFGE), serotyping, and antimicrobial susceptibility testing.
10 quence typing (MLST), plasmid profiling, and antimicrobial susceptibility testing.
11 ted by the NCCLS Subcommittee for Veterinary Antimicrobial Susceptibility Testing.
12 tion's External Quality Assurance System for Antimicrobial Susceptibility Testing.
13 Agar dilution was used to conduct antimicrobial susceptibility testing.
14 -genome short-read sequencing and additional antimicrobial susceptibility testing.
15 to broth microdilution (BMD) for performing antimicrobial susceptibility testing.
16 and was approved by the CLSI Subcommittee on Antimicrobial Susceptibility Testing.
17 serotyping, multilocus sequence typing, and antimicrobial susceptibility testing.
18 sm identification and automated-system-based antimicrobial susceptibility testing.
19 for broad-based bacterial identification or antimicrobial susceptibility testing.
20 nce of accurate organism identification, and antimicrobial susceptibility testing.
21 bolic profiling provides an avenue for rapid antimicrobial susceptibility testing.
23 tandards Institute and European Committee on Antimicrobial Susceptibility Testing agree that carbapen
24 Typhi strains has emerged worldwide, making antimicrobial susceptibility testing an important functi
26 s of 2004 to 2005 and 2009 to 2010 underwent antimicrobial susceptibility testing and characterizatio
27 or additional characterization that included antimicrobial susceptibility testing and detection of fi
28 pulsed-field gel electrophoresis (PFGE) and antimicrobial susceptibility testing and examined for th
29 ne can expect to see changes in guidance for antimicrobial susceptibility testing and interpretation.
33 istance mechanisms in staphylococci, current antimicrobial susceptibility testing and reporting recom
38 ion between the results of existing in vitro antimicrobial susceptibility tests and clinical outcome
39 ovides an effective quantitative measure for antimicrobial susceptibility testing, and determination
40 e now using WGS for pathogen identification, antimicrobial susceptibility testing, and epidemiologica
41 by the VITEK 2 system for identification and antimicrobial susceptibility testing, and the results we
42 terized with routine identification systems, antimicrobial susceptibility testing, and whole-genome s
45 In January 2015, the CLSI Subcommittee on Antimicrobial Susceptibility Testing approved these rang
46 n methods and the lengthy turnaround time of antimicrobial susceptibility testing are significant bar
47 which were outside of the United States, for antimicrobial susceptibility testing as part of the Worl
48 Our results suggest that a rapid and robust antimicrobial susceptibility test (AST) can be construct
50 icular, the absence of FDA-cleared automated antimicrobial susceptibility test (AST) devices that use
55 y Standards Institute (CLSI) Subcommittee on Antimicrobial Susceptibility Testing (AST SC) is a volun
59 , from 56 patients, classified by phenotypic antimicrobial susceptibility testing (AST) as showing re
60 system for rapid pathogen classification and antimicrobial susceptibility testing (AST) at the single
65 . Food and Drug Administration (FDA)-cleared antimicrobial susceptibility testing (AST) devices compa
71 a identification (ID) and rapid yet reliable antimicrobial susceptibility testing (AST) is developed.
77 ds and guidelines (among other products) for antimicrobial susceptibility testing (AST) methods and r
80 ating an urgent need for rapid and sensitive antimicrobial susceptibility testing (AST) methods to gu
83 oenix system for the identification (ID) and antimicrobial susceptibility testing (AST) of 251 isolat
86 Sparks, MD) for the identification (ID) and antimicrobial susceptibility testing (AST) of challenge
88 signed for the rapid identification (ID) and antimicrobial susceptibility testing (AST) of clinically
95 id and reliable bacterial identification and antimicrobial susceptibility testing (AST) remain challe
99 rovide rapid species identification (ID) and antimicrobial susceptibility testing (AST) results for t
101 culture with microbial growth accompanied by antimicrobial susceptibility testing (AST) results in th
102 Concurrently, species, temporal trends, and antimicrobial susceptibility testing (AST) results of Le
103 ast majority of bacterial identification and antimicrobial susceptibility testing (AST) results were
104 stem (AXDX) provides identification (ID) and antimicrobial susceptibility testing (AST) results withi
106 boring MRSA, including three (semi)automated antimicrobial susceptibility testing (AST) systems and f
109 stance has prompted the development of rapid antimicrobial susceptibility testing (AST) technologies
110 sistant Klebsiella pneumoniae demands faster antimicrobial susceptibility testing (AST) to guide anti
111 atory practice in the preanalytical phase of antimicrobial susceptibility testing (AST) was evaluated
112 report form was completed for each case and antimicrobial susceptibility testing (AST) was performed
113 determining the optimal frequency of repeat antimicrobial susceptibility testing (AST) when an organ
116 ISA (hVISA) are pathogens for which accurate antimicrobial susceptibility testing (AST) would rule ou
117 harmacokinetics (PK), pharmacodynamics (PD), antimicrobial susceptibility testing (AST), and how thes
119 k of a rapid pathogen identification (ID) or antimicrobial susceptibility testing (AST), resulting in
120 phokinetic bacterial analysis for phenotypic antimicrobial susceptibility testing (AST), with promisi
130 is an urgent need to develop simple and fast antimicrobial susceptibility tests (ASTs) that allow inf
131 n and facilitates rapid bacterial growth for antimicrobial susceptibility testing at the point of car
132 large surface-to-volume ratio, toward rapid antimicrobial susceptibility testing at the point of car
133 dy were approved by the CLSI Subcommittee on Antimicrobial Susceptibility Testing at their June 2015
134 simple microfluidic device that can perform antimicrobial susceptibility testing automatically via a
135 with an MIC above the European Committee on Antimicrobial Susceptibility Testing breakpoint) when ac
136 ndards Institute revised the fluoroquinolone antimicrobial susceptibility testing breakpoints for bot
139 All isolates were identified and underwent antimicrobial susceptibility testing by broth microdilut
141 through 10 May 2016 underwent routine Etest antimicrobial susceptibility testing by the Hawaii Depar
142 enotypic analysis, including biochemical and antimicrobial susceptibility testing, cellular fatty aci
144 em, were determined by the dielectrophoretic antimicrobial susceptibility testing (dAST) and by the c
145 ical clustering results for MS, genomic, and antimicrobial susceptibility test data to hierarchical c
146 important implications for interpretation of antimicrobial susceptibility testing data and may be imp
148 support from technical representatives from antimicrobial susceptibility testing device manufacturer
150 or =1 microg/ml by the European Committee on Antimicrobial Susceptibility Testing]; disk diffusion br
151 tion's External Quality Assurance System for Antimicrobial Susceptibility Testing (EQAS-AST) from Jan
152 ed in this article, the CLSI Subcommittee on Antimicrobial Susceptibility Testing established new bre
153 ptibility testing, the European Committee on Antimicrobial Susceptibility Testing (EUCAST) and the Cl
154 s Institute (CLSI) and European Committee on Antimicrobial Susceptibility Testing (EUCAST) are 2 glob
155 ntly, clinical FDA and European Committee on Antimicrobial Susceptibility Testing (EUCAST) breakpoint
156 When evaluated using European Committee on Antimicrobial Susceptibility Testing (EUCAST) breakpoint
157 s Institute (CLSI) and European Committee on Antimicrobial Susceptibility Testing (EUCAST) broth micr
158 s Institute (CLSI) and European Committee on Antimicrobial Susceptibility Testing (EUCAST) epidemiolo
159 stitute (CLSI)-FDA and European Committee on Antimicrobial Susceptibility Testing (EUCAST) interpreti
160 s Institute (CLSI) and European Committee of Antimicrobial Susceptibility Testing (EUCAST) methodolog
161 k breakpoints, and the European Committee on Antimicrobial Susceptibility Testing (EUCAST) S. pseudin
162 on (BMD) method of the European Committee on Antimicrobial Susceptibility Testing (EUCAST) was compar
163 stitute (CLSI) and the European Committee on Antimicrobial Susceptibility Testing (EUCAST), respectiv
169 ionization-time of flight mass spectrometry, antimicrobial susceptibility testing followed European C
170 ew method developed and evaluated as a rapid antimicrobial susceptibility test for B. anthracis This
171 enterococci following a laboratory change in antimicrobial susceptibility testing from disk diffusion
175 ofluidic device provides a simple method for antimicrobial susceptibility testing in an automated for
176 ds were approved by the CLSI Subcommittee on Antimicrobial Susceptibility Testing in January 2015 and
177 to 0.5/4 mug/mL) by the CLSI Subcommittee on Antimicrobial Susceptibility Testing in January 2022.
178 terobacteriaceae family poses a challenge to antimicrobial susceptibility testing in the clinical lab
180 tandards Institute and European Committee on Antimicrobial Susceptibility Testing interpretative stan
191 f identification to bacterial species level, antimicrobial susceptibility testing, macrolide resistan
192 health, we advocate for the use of stringent antimicrobial susceptibility test method evaluation proc
193 atory Standards Institute (CLSI) revised the antimicrobial susceptibility testing method for telavanc
194 should consider using a second, independent antimicrobial susceptibility testing method to validate
195 Each organism was tested by the routine antimicrobial susceptibility testing method used by each
198 up organisms on the selection of appropriate antimicrobial susceptibility testing methods and interpr
202 ploying accurate, reproducible, and feasible antimicrobial susceptibility testing methods to guide ap
203 achieved 95% overall agreement with standard antimicrobial susceptibility testing methods, with the h
205 me geographic area using broth microdilution antimicrobial susceptibility testing, multilocus sequenc
209 uld be developed, and the optimal method for antimicrobial susceptibility testing of A. xylosoxidans
212 tion and the agar disk diffusion methods for antimicrobial susceptibility testing of Campylobacter we
213 t represents an accurate tool for performing antimicrobial susceptibility testing of Enterobacterales
215 as been used to reduce the time required for antimicrobial susceptibility testing of Mycobacterium tu
216 s for the performance and quality control of antimicrobial susceptibility testing of Mycoplasma pneum
217 methods decrease the time to identification/antimicrobial susceptibility testing of S. aureus and de
218 ods take several days for identification and antimicrobial susceptibility testing of staphylococcal i
219 in S. aureus, Vitek 2 performed reliably for antimicrobial susceptibility testing of staphylococci an
220 It appears to be an acceptable method for antimicrobial susceptibility testing of staphylococci an
222 control limits and interpretive criteria for antimicrobial susceptibility testing of Streptococcus pn
226 onas maltophilia at this time, and, as such, antimicrobial susceptibility testing of these organisms
227 lity control (QC) standards for the in vitro antimicrobial susceptibility testing of two fastidious v
231 A bloodstream isolates were characterized by antimicrobial susceptibility testing, PCR analysis of vi
233 e isolates were characterized by serotyping, antimicrobial-susceptibility testing, phage typing, and
237 ble S. aureus isolates were characterized by antimicrobial-susceptibility testing, pulsed-field gel e
239 ysis interpretation, culture thresholds, and antimicrobial susceptibility testing, require special co
240 ) CD-ROM on AST, and (iv) the CDC Multilevel Antimicrobial Susceptibility Testing Resource website.
241 pes and correlated with available phenotypic antimicrobial susceptibility test results and genotypic
244 cultures, and BD Phoenix identification and antimicrobial susceptibility test results were comparabl
245 tes, and show that cAST can deliver accurate antimicrobial susceptibility test results within 4-8 h.
246 high degree of correlation of serotyping and antimicrobial susceptibility testing results between fou
247 increased the importance of having accurate antimicrobial susceptibility testing results for guiding
249 logical testing, including interpretation of antimicrobial susceptibility testing results using curre
251 NS category, the organism identification and antimicrobial-susceptibility test results should be conf
254 tant but clindamycin susceptible by in vitro antimicrobial susceptibility testing should be tested fo
255 Based on these findings, we recommend that antimicrobial susceptibility testing should not be routi
257 al and Laboratory Standards Institute (CLSI) Antimicrobial Susceptibility Testing Subcommittee evalua
258 ified selection for changes in motility, and antimicrobial susceptibility testing suggested that the
259 ed in conjunction with the VITEK 2 automated antimicrobial susceptibility test system to ascertain th
262 pid quantitative PCR (qPCR)-based phenotypic antimicrobial susceptibility test that utilizes amplific
263 leading organizations that set standards for antimicrobial susceptibility testing, the European Commi
265 apid ID 32 Strep identification methods, and antimicrobial susceptibility testing to determine their
266 d characterization methods, from traditional antimicrobial susceptibility testing to recent deep-lear
267 , relevant interpretations of the results of antimicrobial susceptibility tests to clinicians, clinic
268 esis (PFGE) following SmaI macrorestriction, antimicrobial susceptibility testing, urease production,
269 human clinical specimens, were subjected to antimicrobial susceptibility testing using a MicroScan W
270 We present a method for rapid and scalable antimicrobial susceptibility testing using stationary na
273 by conventional microbiological methods, and antimicrobial susceptibility test was done by disc diffu
277 lobacter spp. and E. coli were isolated, and antimicrobial susceptibility testing was conducted using
278 e and SCCmec typing were assessed by PCR and antimicrobial susceptibility testing was done according
289 ngoing national surveillance, serotyping and antimicrobial susceptibility testing were done on all pn
290 culture, manual speciation, serotyping, and antimicrobial susceptibility testing were performed at M
292 apid ID 32 Strep identification methods; and antimicrobial susceptibility testing were performed on t
294 Culture-based identification methods and antimicrobial susceptibility testing were used as the re
298 i clinical strain WCHEC13-8 was subjected to antimicrobial susceptibility tests, whole genome sequenc
299 od, Mo.), an established automated method of antimicrobial susceptibility testing with the ability to
300 c device that was capable of executing rapid antimicrobial susceptibility tests with one, two, or eve