Pathogen or Bystander: Clinical Significance of Detecting Human Herpesvirus 6 in Pediatric Cerebrospinal Fluid.


Journal

Journal of clinical microbiology
ISSN: 1098-660X
Titre abrégé: J Clin Microbiol
Pays: United States
ID NLM: 7505564

Informations de publication

Date de publication:
23 04 2020
Historique:
received: 21 02 2020
accepted: 22 02 2020
pubmed: 28 2 2020
medline: 24 6 2021
entrez: 28 2 2020
Statut: epublish

Résumé

Human herpesvirus 6 (HHV-6) is an important cause of meningitis and meningoencephalitis. As testing for HHV-6 in cerebrospinal fluid (CSF) is more readily available using the FilmArray Meningitis/Encephalitis panel (FA-ME; BioFire Diagnostics, Salt Lake City, UT), we aimed to determine the clinical significance of detecting HHV-6 in order to identify true infections and to ensure appropriate antiviral initiation. Chart review on 25 patients positive for HHV-6 by FA-ME was performed to determine clinical presentation, comorbidity, treatment, and outcome. The presence of chromosomally integrated HHV-6 (ciHHV-6) DNA was also investigated. Of 1,005 children tested by FA-ME, HHV-6 was detected in 25 (2.5%). Five patients were diagnosed with either HHV-6 meningitis or meningoencephalitis based on HHV-6 detection in CSF, clinical presentation, and radiographic findings. Detection of HHV-6 by FA-ME led to discontinuation of acyclovir within 12.0 h in all 12 patients empirically treated with acyclovir. Six of the 12 patients were started on ganciclovir therapy within 6.8 h; 4 of these were treated specifically for HHV-6 infection, whereas therapy was discontinued in the remaining 2 patients. CSF parameters were not generally predictive of HHV-6 positivity. The presence of ciHHV-6 was confirmed in 3 of 18 patients who could be tested. Five of the 25 patients included in the study were diagnosed with HHV-6 meningitis/meningoencephalitis. FA-ME results led to discontinuation of empirical antiviral treatment in 12 patients and appropriate initiation of ganciclovir in 4 patients. In our institution, detection of HHV-6 using FA-ME led to faster establishment of disease etiology and optimization of antimicrobial therapy.

Identifiants

pubmed: 32102858
pii: JCM.00313-20
doi: 10.1128/JCM.00313-20
pmc: PMC7180253
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2020 American Society for Microbiology.

Références

J Clin Microbiol. 2020 Feb 24;58(3):
pubmed: 31852767
BMC Genomics. 2018 Mar 20;19(1):204
pubmed: 29554870
J Clin Virol. 2006 Dec;37 Suppl 1:S52-6
pubmed: 17276370
Pediatr Neurol. 2020 Apr;105:10-20
pubmed: 31932119
Rev Med Virol. 2012 May;22(3):144-55
pubmed: 22052666
Clin Infect Dis. 2019 Jun 18;69(1):192-194
pubmed: 30689806
Ann Neurol. 2001 Nov;50(5):612-9
pubmed: 11706967
Pediatr Infect Dis J. 2008 Dec;27(12):1047-51
pubmed: 18989240
J Med Virol. 2010 Oct;82(10):1669-78
pubmed: 20827763
Clin Microbiol Infect. 2020 Mar;26(3):281-290
pubmed: 31760115
Clin Infect Dis. 2005 Mar 15;40(6):890-3
pubmed: 15736026
Clin Infect Dis. 2018 Sep 14;67(7):1125-1128
pubmed: 29635334
J Virol. 2017 Oct 27;91(22):
pubmed: 28835501
Arch Pathol Lab Med. 2015 May;139(5):636-41
pubmed: 25152311
Clin Chem. 2014 May;60(5):765-72
pubmed: 24594780
Pediatrics. 2006 Apr;117(4):1094-100
pubmed: 16585303
Arch Virol. 2014 May;159(5):863-70
pubmed: 24193951
Hosp Pediatr. 2019 Oct;9(10):763-769
pubmed: 31511395
Front Neurol. 2019 Mar 26;10:281
pubmed: 30972012
PLoS One. 2019 Oct 24;14(10):e0223887
pubmed: 31647847
Clin Infect Dis. 2002 Feb 1;34(3):309-17
pubmed: 11774077
J Clin Microbiol. 2018 Mar 26;56(4):
pubmed: 29343540
PLoS One. 2014 Jun 11;9(2):e98819
pubmed: 24919177
J Clin Microbiol. 2017 May;55(5):1557-1565
pubmed: 28275080
J Clin Microbiol. 2018 Apr 25;56(5):
pubmed: 29540454
J Clin Microbiol. 2016 Sep;54(9):2251-61
pubmed: 27335149
J Clin Microbiol. 2016 May;54(5):1223-7
pubmed: 26888901
J Clin Microbiol. 2018 Jun 25;56(7):
pubmed: 29669791
BMJ Case Rep. 2014 Sep 19;2014:
pubmed: 25239996
J Child Neurol. 2007 Nov;22(11):1260-8
pubmed: 18006954
J Clin Microbiol. 2018 Mar 26;56(4):
pubmed: 29436421
J Infect Dis. 2000 Nov;182(5):1321-5
pubmed: 11023456
Clin Infect Dis. 2007 Jun 15;44(12):e118-20
pubmed: 17516391
J Virol Methods. 2008 Nov;153(2):273-5
pubmed: 18703091
Bone Marrow Transplant. 2013 Apr;48(4):574-80
pubmed: 23000642
J Clin Microbiol. 2006 Apr;44(4):1571-4
pubmed: 16597897

Auteurs

Utsav Pandey (U)

Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, California, USA.

Alexander L Greninger (AL)

Department of Laboratory Medicine, University of Washington, Seattle, Washington, USA.
Fred Hutchinson Cancer Research Institute, Seattle, Washington, USA.

Greg R Levin (GR)

Department of Laboratory Medicine, University of Washington, Seattle, Washington, USA.

Keith R Jerome (KR)

Department of Laboratory Medicine, University of Washington, Seattle, Washington, USA.
Fred Hutchinson Cancer Research Institute, Seattle, Washington, USA.

Vikram C Anand (VC)

Division of Infectious Diseases, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, California, USA.
Keck School of Medicine at the University of Southern California, Los Angeles, California, USA.

Jennifer Dien Bard (J)

Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, California, USA jdienbard@chla.usc.edu.
Keck School of Medicine at the University of Southern California, Los Angeles, California, USA.

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