| Literature DB >> 22493336 |
Melissa K Deck1, Erica S Anderson, Rebecca J Buckner, Georgia Colasante, James M Coull, Benjamin Crystal, Phyllis Della Latta, Martin Fuchs, Deanna Fuller, Will Harris, Kevin Hazen, Lisa L Klimas, Daniel Lindao, Michelle C Meltzer, Margie Morgan, Janeen Shepard, Sharon Stevens, Fann Wu, Mark J Fiandaca.
Abstract
A novel rapid peptide nucleic acid fluorescence in situ hybridization (FISH) method, Staphylococcus QuickFISH, for the direct detection of Staphylococcus species from positive blood culture bottles was evaluated in a multicenter clinical study. The method utilizes a microscope slide with predeposited positive- and negative-control organisms and a self-reporting 15-min hybridization step, which eliminates the need for a wash step. Five clinical laboratories tested 722 positive blood culture bottles containing gram-positive cocci in clusters. The sensitivities for detection of Staphylococcus aureus and coagulase-negative staphylococci (CoNS) were 99.5% (217/218) and 98.8% (487/493), respectively, and the combined specificity of the assay was 89.5% (17/19). The combined positive and negative predictive values of the assay were 99.7% (696/698) and 70.8% (17/24), respectively. Studies were also performed on spiked cultures to establish the specificity and performance sensitivity of the method. Staphylococcus QuickFISH has a turnaround time (TAT) of <30 min and a hands-on time (HOT) of <5 min. The ease and speed of the method have the potential to improve the accuracy of therapeutic intervention by providing S. aureus/CoNS identification simultaneously with Gram stain results.Entities:
Mesh:
Year: 2012 PMID: 22493336 PMCID: PMC3372102 DOI: 10.1128/JCM.00225-12
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948