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      Rapid Diagnosis of Infection in the Critically Ill, a Multicenter Study of Molecular Detection in Bloodstream Infections, Pneumonia, and Sterile Site Infections*

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          Abstract

          Supplemental Digital Content is available in the text.

          Objective:

          Early identification of causative microorganism(s) in patients with severe infection is crucial to optimize antimicrobial use and patient survival. However, current culture-based pathogen identification is slow and unreliable such that broad-spectrum antibiotics are often used to insure coverage of all potential organisms, carrying risks of overtreatment, toxicity, and selection of multidrug-resistant bacteria. We compared the results obtained using a novel, culture-independent polymerase chain reaction/electrospray ionization-mass spectrometry technology with those obtained by standard microbiological testing and evaluated the potential clinical implications of this technique.

          Design:

          Observational study.

          Setting:

          Nine ICUs in six European countries.

          Patients:

          Patients admitted between October 2013 and June 2014 with suspected or proven bloodstream infection, pneumonia, or sterile fluid and tissue infection were considered for inclusion.

          Interventions:

          None.

          Measurements and Main Results:

          We tested 616 bloodstream infection, 185 pneumonia, and 110 sterile fluid and tissue specimens from 529 patients. From the 616 bloodstream infection samples, polymerase chain reaction/electrospray ionization-mass spectrometry identified a pathogen in 228 cases (37%) and culture in just 68 (11%). Culture was positive and polymerase chain reaction/electrospray ionization-mass spectrometry negative in 13 cases, and both were negative in 384 cases, giving polymerase chain reaction/electrospray ionization-mass spectrometry a sensitivity of 81%, specificity of 69%, and negative predictive value of 97% at 6 hours from sample acquisition. The distribution of organisms was similar with both techniques. Similar observations were made for pneumonia and sterile fluid and tissue specimens. Independent clinical analysis of results suggested that polymerase chain reaction/electrospray ionization-mass spectrometry technology could potentially have resulted in altered treatment in up to 57% of patients.

          Conclusions:

          Polymerase chain reaction/electrospray ionization-mass spectrometry provides rapid pathogen identification in critically ill patients. The ability to rule out infection within 6 hours has potential clinical and economic benefits.

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          Most cited references30

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          A Coefficient of Agreement for Nominal Scales

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            The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine.

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              Duration of hypotension before initiation of effective antimicrobial therapy is the critical determinant of survival in human septic shock*

              Critical Care Medicine, 34(6), 1589-1596
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                Author and article information

                Journal
                Crit Care Med
                Crit. Care Med
                CCM
                Critical Care Medicine
                Lippincott Williams & Wilkins
                0090-3493
                1530-0293
                November 2015
                15 November 2015
                : 43
                : 11
                : 2283-2291
                Affiliations
                [1 ]Department of Intensive Care, Erasme Hospital, Université Libre de Bruxelles, Brussels, Belgium.
                [2 ]Division of Critical Care, University College London Hospitals NIHR Biomedical Research Centre and Bloomsbury Institute of Intensive Care Medicine, University College Hospital, London, United Kingdom.
                [3 ]Department of Anesthesiology and Critical Care, Val de Grâce Military Hospital, Paris, France.
                [4 ]Intensive Care Unit, Department of Anesthesiology, Pharmacology and Intensive Care, University Hospitals of Geneva, Geneva, Switzerland.
                [5 ]Barts and The London School of Medicine and Dentistry, Queen Mary University of London and Barts Health NHS Trust, London, United Kingdom.
                [6 ]Klinik für Anästhesiologie, Intensivmedizin und Schmerztherapie, Universitätsklinikum Frankfurt, Frankfurt am Main, Germany.
                [7 ]1st Clinic of Anaesthesia and Intensive Care of Warsaw Medical University, Warsaw, Poland.
                [8 ]Genomic Research Laboratory, Department of Internal Medicine, Service of Infectious Diseases, University of Geneva Hospitals, Geneva, Switzerland.
                [9 ]Department of Microbiology, Saint Louis University Hospital, Paris, France.
                [10 ]Abbott GmbH & Co. KG, Wiesbaden, Germany.
                [11 ]Ibis Biosciences, Abbott, Carlsbad, CA.
                Author notes
                For information regarding this article, E-mail: jlvincen@ 123456ulb.ac.be
                Article
                00003
                10.1097/CCM.0000000000001249
                4603364
                26327198
                45c2887e-7032-4d87-95d3-b9ee3ef5dfb7
                Copyright © 2015 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. All Rights Reserved.

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.

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                critically ill,culture-independent,early diagnosis,infection,microbiology,molecular detection

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