Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractAir ionization as a control technology for off-gas emissions of volatile organic compounds    Next AbstractDefining gu-soo perception in Doenjang (fermented soybean paste) using consumer tests with limited sensory modality and instrumental analysis »

Eur J Clin Microbiol Infect Dis


Title:"Evaluation of a sterile, filter-based, in-house method for rapid direct bacterial identification and antimicrobial susceptibility testing using positive blood culture"
Author(s):Kim KJ; Yun SG; Cho Y; Nam MH; Ko YJ; Lee CK;
Address:"Department of Laboratory Medicine, College of Medicine, Korea University, Seoul, Korea. Department of Laboratory Medicine, College of Medicine, Chosun University, Gwangju, Korea. Department of Laboratory Medicine, College of Medicine, Korea University, Seoul, Korea. cklee5381@gmail.com"
Journal Title:Eur J Clin Microbiol Infect Dis
Year:2023
Volume:20230403
Issue:6
Page Number:691 - 700
DOI: 10.1007/s10096-023-04592-y
ISSN/ISBN:1435-4373 (Electronic) 0934-9723 (Linking)
Abstract:"This study aimed to assess the performance of our in-house method for rapid direct bacterial identification (ID) and antimicrobial susceptibility testing (AST) using a positive blood culture (BC) broth. For Gram-negative bacteria, 4 mL of BC broth was aspirated and passed through a Sartorius Minisart syringe filter with a pore size of 5 microm. The filtrate was then centrifuged and washed. A small volume of the pellet was used for ID, using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, and for AST, using automated broth microdilution. For Gram-positive cocci, 4 mL of BC broth was passed through the Minisart syringe filter. Then, 4 mL of sterile distilled water was injected in the direction opposite to that of the filtration to collect the bacterial residue trapped in the filter. Compared with the conventional method performed with pure colonies on agar plates, 94.0% (234/249) were correctly identified using the in-house method, with rates of 91.4% (127/139) and 97.3% (107/110) for Gram-positive and Gram-negative isolates, respectively. Of 234 correctly identified isolates, 230 were assessed by AST. Categorical agreement and essential agreement were 93.3% and 94.5%, respectively, with a minor error rate of 3.8%, a major error rate of 3.4%, and a very major error rate of 1.6%. Our in-house preparation method showed good performance in rapid direct ID and AST using positive BC broths compared to the conventional method. This simple method can shorten the conventional turnaround time for ID and AST by at least 1 day, potentially contributing to better patient management"
Keywords:"Humans *Anti-Bacterial Agents/pharmacology Blood Culture/methods Microbial Sensitivity Tests Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods Bacteria Gram-Negative Bacteria *Bacteremia/diagnosis/microbiology Antimicrobial susceptib;"
Notes:"MedlineKim, Keun Ju Yun, Seung Gyu Cho, Yunjung Nam, Myung-Hyun Ko, Young Jin Lee, Chang Kyu eng Germany 2023/04/04 Eur J Clin Microbiol Infect Dis. 2023 Jun; 42(6):691-700. doi: 10.1007/s10096-023-04592-y. Epub 2023 Apr 3"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 22-11-2024