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Should there be a standardised approach to the diagnostic workup of suspected adult encephalitis? A case series from Australia

dc.contributor.authorHuppatz, Clare
dc.contributor.authorGawarikar, Yash
dc.contributor.authorLevi, Chris
dc.contributor.authorKelly, Paul M
dc.contributor.authorWilliams, David
dc.contributor.authorDalton, Craig
dc.contributor.authorMassey, Peter
dc.contributor.authorGivney, Rodney
dc.contributor.authorDurrheim, David N
dc.date.accessioned2016-01-18T03:10:50Z
dc.date.available2016-01-18T03:10:50Z
dc.date.issued2010-12-15
dc.date.updated2016-02-24T08:08:12Z
dc.description.abstractBACKGROUND The clinical diagnosis of encephalitis is often difficult and identification of a causative organism is infrequent. The encephalitis syndrome may herald the emergence of novel pathogens with outbreak potential. Individual treatment and an effective public health response rely on identifying a specific pathogen. In Australia there have been no studies to try to improve the identification rate of encephalitis pathogens. This study aims to review the diagnostic assessment of adult suspected encephalitis cases. METHODS A retrospective clinical audit was performed, of all adult encephalitis presentations between July 1998 and December 2007 to the three hospitals with adult neurological services in the Hunter New England area, northern New South Wales, Australia. Case notes were examined for evidence of relevant history taking, clinical features, physical examination, laboratory and neuroradiology investigations, and outcomes. RESULTS A total of 74 cases were included in the case series. Amongst suspected encephalitis cases, presenting symptoms and signs included fever (77.0%), headache (62.1%), altered consciousness (63.5%), lethargy (32.4%), seizures (25.7%), focal neurological deficits (31.1%) and photophobia (17.6%). The most common diagnostic laboratory test performed was cerebrospinal fluid (CSF) analysis (n = 67, 91%). Herpes virus polymerase chain reaction (n = 53, 71.6%) and cryptococcal antigen (n = 46, 62.2%) were the antigenic tests most regularly performed on CSF. Neuroradiological procedures employed were computerized tomographic brain scanning (n = 68, 91.9%) and magnetic resonance imaging of the brain (n = 35, 47.3%). Thirty-five patients (47.3%) had electroencephalograms. The treating clinicians suspected a specific causative organism in 14/74 cases (18.9%), of which nine (12.1%) were confirmed by laboratory testing. CONCLUSIONS The diagnostic assessment of patients with suspected encephalitis was not standardised. Appropriate assessment is necessary to exclude treatable agents and identify pathogens warranting public health interventions, such as those transmitted by mosquitoes and those that are vaccine preventable. An algorithm and guidelines for the diagnostic workup of encephalitis cases would assist in optimising laboratory testing so that clinical management can be best tailored to the pathogen, and appropriate public health measures implemented.
dc.description.sponsorshipThe Master of Applied Epidemiology Program (CH and PK) is funded by the Australian Government Department of Health and Ageing. PK's salary is supported by Australia's National Health and Medical Research Council.en_AU
dc.identifier.issn1471-2334en_AU
dc.identifier.urihttp://hdl.handle.net/1885/95504
dc.publisherBioMed Central
dc.rights© 2010 Huppatz et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.sourceBMC Infectious Diseases
dc.subjectadmitting department, hospital
dc.subjectadult
dc.subjectdiagnostic tests, routine
dc.subjectencephalitis
dc.subjecthumans
dc.subjectnew south wales
dc.subjectretrospective studies
dc.subjectmedical audit
dc.titleShould there be a standardised approach to the diagnostic workup of suspected adult encephalitis? A case series from Australia
dc.typeJournal article
local.bibliographicCitation.issue1en_AU
local.bibliographicCitation.startpage353en_AU
local.contributor.affiliationHuppatz, Clare, College of Medicine, Biology and Environment, CMBE Research School of Population Health, Natl Centre for Epidemiology & Population Health, The Australian National Universityen_AU
local.contributor.affiliationGawarikar, Yash, NSW Health, Australiaen_AU
local.contributor.affiliationLevi, Christopher, John Hunter Hospital, Australiaen_AU
local.contributor.affiliationKelly, Paul, College of Medicine, Biology and Environment, CMBE Research School of Population Health, Natl Centre for Epidemiology & Population Health, The Australian National Universityen_AU
local.contributor.affiliationWilliams, David, John Hunter Hospital, Australiaen_AU
local.contributor.affiliationDalton, Craig, Commonwealth Department of Health and Ageing, Australiaen_AU
local.contributor.affiliationMassey, Peter, Hunter New England Population Health, Australiaen_AU
local.contributor.affiliationGivney, Rodney, University of Newcastle, Australiaen_AU
local.contributor.affiliationDurrheim, David N, University of Newcastle, Australiaen_AU
local.contributor.authoruidU4323806en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor111799en_AU
local.identifier.ariespublicationf2965xPUB1018en_AU
local.identifier.citationvolume10en_AU
local.identifier.doi10.1186/1471-2334-10-353en_AU
local.identifier.essn1471-2334en_AU
local.identifier.scopusID2-s2.0-78650037204
local.identifier.thomsonID000286055200001
local.publisher.urlhttp://www.biomedcentral.com/en_AU
local.type.statusPublished Versionen_AU

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