JCM Accepted Manuscript Posted Online 9 December 2015 J. Clin. Microbiol. doi:10.1128/JCM.02913-15 Copyright © 2015, American Society for Microbiology. All Rights Reserved.
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Diagnostic performance of galactomannan antigen testing in cerebrospinal fluid
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G.M. Chong1#, J.A. Maertens2, K. Lagrou3, G.J. Driessen4, J.J. Cornelissen5, B.J.A. Rijnders1
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the Netherlands.
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Leuven, Department of Haematology, Leuven, Belgium.
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KU Leuven- University of Leuven, Department of Microbiology and Immunology, Leuven, Belgium.
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Erasmus University Medical Center, Sophia Children’s Hospital, subdepartment of Paediatric Infectious
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Disease and Immunology, Rotterdam, the Netherlands.
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Erasmus University Medical Center, Department of Internal Medicine, Infectious Diseases, Rotterdam,
KU Leuven- University of Leuven, Department of Microbiology and Immunology; University Hospitals
Erasmus University Medical Center, Department of Haematology, Rotterdam, the Netherlands.
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Running title: Galactomannan antigen testing in cerebrospinal fluid
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#Corresponding author
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G.M. Chong, MD.
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Department of Internal Medicine, Infectious Diseases.
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Erasmus University Medical Center.
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Room Na-922, PB2040, 3000 CA Rotterdam, the Netherlands.
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Email address:
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Tel. +31644533371
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Fax. +31107033875
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Manuscript category: Original article.
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Abstract word count: 223.
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Text word count: 1680.
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Table: 4 tables, 1 figure.
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References: 7.
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Keywords: cerebral aspergillosis, galactomannan antigen testing, cerebrospinal fluid.
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Abstract
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Introduction
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Testing cerebrospinal fluid (CSF) for the presence of galactomannan (GM) antigen may help in
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diagnosing cerebral aspergillosis (CA). However, the use of CSF GM as a diagnostic test never been
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validated. We evaluated its diagnostic performance by comparing the CSF GM levels at different cut-offs
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in patients with probable and proven CA to those without CA.
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Methods
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Patients from 2 tertiary referral hospitals with suspected CA between 2004-2014 and in whom CSF GM
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had been determined, were selected. EORTC/MSG definitions of invasive aspergillosis and CA were
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used but excluding the to-be-validated-test (=CSF GM) as a microbiological EORTC/MSG criterion.
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Results
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The study population consisted of 44 patients (4 proven CA, 13 probable CA and 27 no CA). Of the 17
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patients with CA, 15 had a CSF GM of ≥2.0. In patients without CA, 26 of the 27 had a CSF GM of