2016
DOI: 10.1016/j.eimc.2014.11.014
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Antibiograma rápido en Microbiología Clínica

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Cited by 13 publications
(4 citation statements)
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“…It takes approximately 12 hr for a conventional PCR to perform, and this is partitioned into three important steps. The first step is DNA extraction, which is followed by the second step consisting of DNA amplification in a thermocycler, and then the detection of amplified DNA materials in gel electrophoresis (Rosselló & Pérez, 2016). this method is that you need to extract the DNA of so many different bacteria from different environmental sample matrices to be able to compare (Franklin, Aga, et al, 2016).…”
Section: Polymerase Chain Reactionmentioning
confidence: 99%
See 1 more Smart Citation
“…It takes approximately 12 hr for a conventional PCR to perform, and this is partitioned into three important steps. The first step is DNA extraction, which is followed by the second step consisting of DNA amplification in a thermocycler, and then the detection of amplified DNA materials in gel electrophoresis (Rosselló & Pérez, 2016). this method is that you need to extract the DNA of so many different bacteria from different environmental sample matrices to be able to compare (Franklin, Aga, et al, 2016).…”
Section: Polymerase Chain Reactionmentioning
confidence: 99%
“…The MALDI-TOF MS identifies bacteria, yeast, and filamentous molds in a couple of minutes using protein analysis (Rosselló & Pérez, 2016). During antibiogram, MALDI-TOF MS predicts whether a bacteria harbors enzyme that hydrolyzes antibiotics, such as ESBLs and carbapenemases in approximately three hours.…”
Section: Maldi-tof Mass Spectrometrymentioning
confidence: 99%
“…In enterococci, seven Enterococcus faecalis and three Enterococcus faecium were tested against Ampicillin, Vancomycin and Ciprofloxacin at concentrations of 32, 16 The results of susceptibility obtained at 35 • C from colonies grown in culture plates by means of the commercial methods VITEK2 (bioMérieux, Marcy l'Etoile, France), MicroScan (Siemens, Tarrytown, NY, USA) and E-test (Liofilchem, Roseto Degli Abruzzi, Italy), applying the criteria published by the EUCAST, 9 were considered as the gold standard. Finally, results obtained by ATPbioluminescence were compared to the gold standard according to FDA criteria 10 ; agreements and disagreements among the susceptibility values obtained were classified as agreements, very major errors (false susceptibility), major errors (false resistance), or minor errors (susceptible/resistant versus intermediate susceptibility).…”
Section: Validation Proceduresmentioning
confidence: 99%
“…Several AST methods have been established, such as the disk diffusion method based on solid-plate AST, the broth dilution method for liquid AST, and polymerase chain reactionbased methods [7]. Recently, numerous rapid AST methods based on microfluidic systems with microscopic analysis have been developed to reduce the time for AST and to increase the accuracy, but the inoculum effects of those methods have not been studied [8][9][10][11][12].…”
Section: Introductionmentioning
confidence: 99%