Abstract

The reference method for the diagnosis of bloodstream infections is blood culture followed by biochemical identification and antibiotic susceptibility testing of the isolated pathogen. This process requires 48 to 72 hours. The rapid administration of the most appropriate antimicrobial treatment is crucial for the survival of septic patients; therefore, a rapid method that enables diagnosis directly from analysis of a blood sample without culture is needed. A recently developed platform that couples broad-range PCR amplification of pathogen DNA with electrospray ionization mass spectrometry (PCR/ESI-MS) has the ability to identify virtually any microorganism from direct clinical specimens. To date, two clinical evaluations of the PCR/ESI-MS technology for the diagnosis of bloodstream infections from whole blood have been published. Here we discuss them and describe recent improvements that result in an enhanced sensitivity. Other commercially available assays for the molecular diagnosis of bloodstream infections from whole blood are also reviewed. The use of highly sensitive molecular diagnostic methods in combination with conventional procedures could substantially improve the management of septic patients.

Highlights

  • Bloodstream infection is a life-threatening condition that results from the presence of microorganisms, generally bacteria or fungi, in the blood [1]

  • This review describes the current status of the molecular diagnosis of sepsis with emphasis on the PCR/ESI-MS technology

  • Microbiological diagnosis has historically relied on culture

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Summary

Introduction

Bloodstream infection is a life-threatening condition that results from the presence of microorganisms, generally bacteria or fungi, in the blood [1]. Every hour of delay in initiation of appropriate antimicrobial therapy increases the mortality by 7.6% in patients with septic shock [3]. Conventional methods for the microbiological diagnosis of sepsis rely on blood culture followed by biochemical identification. It usually takes 1 to 3 days to obtain both the identification and the antimicrobial susceptibility profile of the pathogen. The major limitation of blood culture methods is that they require a median timeto-positivity of 12 to 17 hours [4]. Another limitation of this method is that the presence of unculturable or fastidious microorganisms may decrease its sensitivity. There is an urgent need to improve the diagnostic tools for a better management of septic patients

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