ISO. First edition. Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation. ISO () Clinical laboratory testing and in vitro diagnostic test systems – Susceptibility testing of infectious agents and evaluation of performance of. Buy ISO , Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices, Part 1, at CLSI.
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Stock solutions and microdilution wells were tested for concentration of antifungal agent using high-performance liquid chromatography HPLC methods previously described 125. Breakpoints for short incubation Expert rules and intrinsic resistance Resistance mechanisms Guidance documents Consultations – New! International Organization for Standards.
Development and validation of a high-performance liquid chromatographic assay for the determination of fluconazole in human whole blood using solid phase extraction. Single-step iao of fluconazole from plasma by ultra-filtration for the measurement of its free concentration by high performance liquid chromatography.
In summary, our data suggest that microdilution trays for hydrophilic drugs such as FLC can be accurately prepared following the ISO recommendations or the serial 2-fold dilution schemes. All statistical analyses were done with the statistical package PAWS statistics Reference method for testing the in vitro activity of io agents against rapidly growing aerobic bacteria involved in infectious diseases.
Selective high-performance liquid chromatographic assay for itraconazole and hydroxyitraconazole in plasma from human immunodeficiency virus-infected patients. Journal List J Clin Microbiol v. These documents are available for purchase from ISO or national standards organisations.
Reference method for broth dilution antifungal susceptibility testing of yeast, 3rd ed. ECDC documents of relevance to antimicrobial susceptibility testing. Simultaneous quantification of voriconazole and posaconazole in human plasma by high-performance liquid chromatography with ultra-violet detection.
Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing anaerobic bacteria involved in infectious diseases. While this is the gold standard for preparation of dilution series, the question has risen if modern pipettes are sufficiently precise to allow dilution series to be prepared as serial dilutions without a loss of accuracy.
Sitemap Search close sitemap. Furthermore, previous studies have demonstrated a much higher interlaboratory variation in MIC results for quality control strains for itraconazole than for flucytosine and fluconazole 6 – 8. Microtiter plates were prepared according to the ISO standard and by serial dilution procedures recommended for preparation of trays of both hydrophilic and hydrophobic drugs 9 Example of a quick liquid chromatographic assay of itraconazole in serum.
ECDC roadmap for integration of molecular typing and genomic typing into European-level surveillance and epidemic preparedness — Version 2. The greatest discrepancy was observed for the lowest concentrations and for the dilutions prepared outside Spain and shipped for concentration determinations.
EUCAST: External documents
Precision of itraconazole dilution series by procedure and laboratory a. Evaluation of performance of antimicrobial susceptibility test devices. Splitting wild type distributions. Quality control procedures of AST should be implemented in order to minimize izo inaccuracy of dilution methods and lack of reproducibility when hydrophobic compounds such as ITC are tested.
Relevant external documents
ISO Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 2: Acknowledgments We have no conflict of interest to declare.