Literature DB >> 20569815

Molecular diagnosis of neonatal sepsis.

Jeanne A Jordan1.   

Abstract

Several molecular testing options are now or will soon be available for diagnosing bloodstream infections in the neonate. The advantages include the speed at which results would be available and the ability to use those results to tailor empirical therapy and reduce the amount of unnecessary or ineffective antibiotics an infant receives. However, there are still difficult challenges before this potential can be realized. A variety of technological advances are needed, including (1) improved recovery of microorganisms in whole blood extractions, (2) increased assay sensitivity, (3) simpler testing platforms that could be run 24/7, and (4) more assays to detect antibiotic resistance genes to reduce reliance on culture-based protocols for antimicrobial susceptibility testing. Although considerable hurdles remain, this challenge is now a priority for investigators in academia and industry.

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Year:  2010        PMID: 20569815     DOI: 10.1016/j.clp.2010.02.001

Source DB:  PubMed          Journal:  Clin Perinatol        ISSN: 0095-5108            Impact factor:   3.430


  4 in total

1.  Evaluation of MolYsis™ Complete5 DNA extraction method for detecting Staphylococcus aureus DNA from whole blood in a sepsis model using PCR/pyrosequencing.

Authors:  Chase D McCann; Jeanne A Jordan
Journal:  J Microbiol Methods       Date:  2014-02-03       Impact factor: 2.363

Review 2.  Molecular assays for the diagnosis of sepsis in neonates.

Authors:  Mohan Pammi; Angela Flores; James Versalovic; Mariska Mg Leeflang
Journal:  Cochrane Database Syst Rev       Date:  2017-02-25

Review 3.  Biomarkers for late-onset neonatal sepsis: cytokines and beyond.

Authors:  Pak C Ng; Hugh S Lam
Journal:  Clin Perinatol       Date:  2010-09       Impact factor: 3.430

4.  Performance of a Novel Molecular Method in the Diagnosis of Late-Onset Sepsis in Very Low Birth Weight Infants.

Authors:  Jonathan Davis; Sharon Christie; Derek Fairley; Peter Coyle; Richard Tubman; Michael D Shields
Journal:  PLoS One       Date:  2015-08-25       Impact factor: 3.240

  4 in total

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