Literature DB >> 20920896

Improved early diagnosis of Pseudomonas aeruginosa by real-time PCR to prevent chronic colonisation in a paediatric cystic fibrosis population.

Elaine McCulloch1, Carol Lucas, Gordon Ramage, Craig Williams.   

Abstract

Early detection of Pseudomonas aeruginosa in children with cystic fibrosis is hampered by the need to process a sub-optimal specimen type, namely cough swabs, which are known to have a lower positive yield than sputa or more invasive samples. This delay in the detection of low levels of P. aeruginosa could potentially result in the loss of an opportunity to initiate early aggressive antibiotic therapy and result in chronic colonisation, with a poorer overall prognosis. Quantitative real-time PCR (qPCR) offers an opportunity to increase the detection rate of P. aeruginosa compared to traditional culture techniques. This study examined 500 cough swabs and 42 sputum samples from paediatric patients and showed that detection of P. aeruginosa could be increased in both sample types by 100% and 45% respectively. Overall the sensitivity was 100% and specificity of 58% when compared to culture as a gold standard. These results although initially promising require careful consideration both from a treatment and infection control standpoint as the significance of detection of very low levels of P. aeruginosa is unclear. Copyright Â
© 2010 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 20920896     DOI: 10.1016/j.jcf.2010.09.001

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  6 in total

1.  Pseudomonas aeruginosa serology and risk for re-isolation in the EPIC trial.

Authors:  Michael Anstead; Sonya L Heltshe; Umer Khan; Joseph T Barbieri; Markus Langkamp; Gerd Döring; Shimoni Dharia; Ronald L Gibson; Miriam M Treggiari; James Lymp; Margaret Rosenfeld; Bonnie Ramsey
Journal:  J Cyst Fibros       Date:  2012-09-01       Impact factor: 5.482

2.  Proposal of a quantitative PCR-based protocol for an optimal Pseudomonas aeruginosa detection in patients with cystic fibrosis.

Authors:  Florence Le Gall; Rozenn Le Berre; Sylvain Rosec; Jeanne Hardy; Stéphanie Gouriou; Sylvie Boisramé-Gastrin; Sophie Vallet; Gilles Rault; Christopher Payan; Geneviève Héry-Arnaud
Journal:  BMC Microbiol       Date:  2013-06-21       Impact factor: 3.605

3.  A novel multiplex PCR for detection of Pseudomonas aeruginosa: A major cause of wound infections.

Authors:  Muhammad Salman; Aamir Ali; Abdul Haque
Journal:  Pak J Med Sci       Date:  2013-07       Impact factor: 1.088

4.  Detection of algD, oprL and exoA Genes by New Specific Primers as an Efficient, Rapid and Accurate Procedure for Direct Diagnosis of Pseudomonas aeruginosa Strains in Clinical Samples.

Authors:  Sedighe Rashno Taee; Behzad Khansarinejad; Hamid Abtahi; Mohammad Najafimosleh; Ehsanollah Ghaznavi-Rad
Journal:  Jundishapur J Microbiol       Date:  2014-10-01       Impact factor: 0.747

5.  Development of uracil-DNA-glycosylase-supplemented loop-mediated isothermal amplification coupled with nanogold probe (UDG-LAMP-AuNP) for specific detection of Pseudomonas aeruginosa.

Authors:  Orapan Manajit; Siwaporn Longyant; Paisarn Sithigorngul; Parin Chaivisuthangkura
Journal:  Mol Med Rep       Date:  2018-02-02       Impact factor: 2.952

6.  Evaluation of Clarithromycin Resistance Among Iranian Helicobacter pylori Isolates by E-Test and Real-Time Polymerase Chain Reaction Methods.

Authors:  Mojdeh Hakemi Vala; Shirin Eyvazi; Hossein Goudarzi; Hamid Reza Sarie; Mehrdad Gholami
Journal:  Jundishapur J Microbiol       Date:  2016-03-19       Impact factor: 0.747

  6 in total

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