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Rapid qualitative urinary tract infection pathogen identification by SeptiFast real-time PCR

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BORIS DOI
10.7892/boris.6055
Date of Publication
2011
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Author
Lehmann, Lutz Ericorcid-logo
Universitätsklinik für Anästhesiologie und Schmerztherapie
Hauser, Stefan
Malinka, Thomas
Klaschik, Sven
Weber, Stefan U
Schewe, Jens-Christian
Stüber, Frank
Universitätsklinik für Anästhesiologie und Schmerztherapie
Book, Malte
Universitätsklinik für Anästhesiologie und Schmerztherapie
Series
PLoS ONE
ISSN or ISBN (if monograph)
1932-6203
Publisher
Public Library of Science
Language
English
Publisher DOI
10.1371/journal.pone.0017146
PubMed ID
21359187
Description
Background

Urinary tract infections (UTI) are frequent in outpatients. Fast pathogen identification is mandatory for shortening the time of discomfort and preventing serious complications. Urine culture needs up to 48 hours until pathogen identification. Consequently, the initial antibiotic regimen is empirical.
Aim

To evaluate the feasibility of qualitative urine pathogen identification by a commercially available real-time PCR blood pathogen test (SeptiFast®) and to compare the results with dipslide and microbiological culture.
Design of study

Pilot study with prospectively collected urine samples.
Setting

University hospital.
Methods

82 prospectively collected urine samples from 81 patients with suspected UTI were included. Dipslide urine culture was followed by microbiological pathogen identification in dipslide positive samples. In parallel, qualitative DNA based pathogen identification (SeptiFast®) was performed in all samples.
Results

61 samples were SeptiFast® positive, whereas 67 samples were dipslide culture positive. The inter-methodological concordance of positive and negative findings in the gram+, gram- and fungi sector was 371/410 (90%), 477/492 (97%) and 238/246 (97%), respectively. Sensitivity and specificity of the SeptiFast® test for the detection of an infection was 0.82 and 0.60, respectively. SeptiFast® pathogen identifications were available at least 43 hours prior to culture results.
Conclusion

The SeptiFast® platform identified bacterial DNA in urine specimens considerably faster compared to conventional culture. For UTI diagnosis sensitivity and specificity is limited by its present qualitative setup which does not allow pathogen quantification. Future quantitative assays may hold promise for PCR based UTI pathogen identification as a supplementation of conventional culture methods.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/76617
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journal.pone.0017146.pdftextAdobe PDF133.01 KBpublishedOpen
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