ArticleJournal of clinical microbiology2005
Direct identification of major blood culture pathogens, including Pseudomonas aeruginosa and Escherichia coli, by a panel of fluorescence in situ hybridization assays using peptide nucleic acid probes.
Article in Journal of clinical microbiology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
What it found
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The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
17 citing papers in PubMed.
- Quality Control in Diagnostic Fluorescence In Situ Hybridization (FISH) in Microbiology.Methods in molecular biology (Clifton, N.J.) · 2021Article
- Clinical Utility of PNA-FISH for Burn Wound Diagnostics: A Noninvasive, Culture-Independent Technique for Rapid Identification of Pathogenic Organisms in Burn Wounds.Journal of burn care & research : official publication of the American Burn Association · 2019Article
- Evaluation of FISH for Blood Cultures under Diagnostic Real-Life Conditions.European journal of microbiology & immunology · 2018Article
- Identification of pathogenic bacteria in complex samples using a smartphone based fluorescence microscope.RSC advances · 2018Article
- New and developing diagnostic technologies for urinary tract infections.Nature reviews. Urology · 2017Review
- Developments for improved diagnosis of bacterial bloodstream infections.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2014Review
- A new multiplex polymerase chain reaction assay for the identification a panel of bacteria involved in bacteremia.Advanced biomedical research · 2013Article
- Rapid detection of Pseudomonas aeruginosa from positive blood cultures by quantitative PCR.Annals of clinical microbiology and antimicrobials · 2010Article
- Fluorescence in situ hybridization method using a peptide nucleic acid probe for identification of Salmonella spp. in a broad spectrum of samples.Applied and environmental microbiology · 2010Article
- Real-time identification of bacteria and Candida species in positive blood culture broths by matrix-assisted laser desorption ionization-time of flight mass spectrometry.Journal of clinical microbiology · 2010Article
- Rapid identification of bacteria in positive blood culture broths by matrix-assisted laser desorption ionization-time of flight mass spectrometry.Journal of clinical microbiology · 2010Article
- Development and application of a novel peptide nucleic acid probe for the specific detection of Cronobacter genomospecies (Enterobacter sakazakii) in powdered infant formula.Applied and environmental microbiology · 2009Article
- Rapid identification of pathogenic yeast isolates by real-time PCR and two-dimensional melting-point analysis.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2007Article
- First notification of positive blood cultures and the high accuracy of the gram stain report.Journal of clinical microbiology · 2007Article
- Current molecular techniques for the detection of microbial pathogens.Science progress · 2007Review
- Rapid identification of pathogens in blood cultures with a modified fluorescence in situ hybridization assay.Journal of clinical microbiology · 2006Article
- Faster identification of pathogens in positive blood cultures by fluorescence in situ hybridization in routine practice.Journal of clinical microbiology · 2006Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Rapid identification of four major pathogens from 1,231 positive blood cultures by fluorescence in situ hybridization with peptide nucleic acid probes (AdvanDx Inc., Woburn, Mass.) was evaluated. For Escherichia coli, Staphylococcus aureus, and Candida albicans results agreed with conventional identification. The lower sensitivity of the Pseudomonas aeruginosa assay should not compromise the utility of the four assays.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.