Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/29260
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dc.contributor.authorHughes C.M.en
dc.contributor.authorDendle C.en
dc.contributor.authorRadalage R.en
dc.contributor.authorSpring S.en
dc.contributor.authorGraham M.en
dc.contributor.authorRogers B.A.en
dc.date.accessioned2021-05-14T09:52:51Zen
dc.date.available2021-05-14T09:52:51Zen
dc.date.copyright2020en
dc.date.created20200526en
dc.date.issued2020-05-26en
dc.identifier.citationPathology. 52 (4) (pp 478-482), 2020. Date of Publication: June 2020.en
dc.identifier.issn0031-3025en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/29260en
dc.description.abstractMultiplex polymerase chain reaction (PCR) testing has revolutionised microbiological practice but also increased the number of positive results of uncertain significance. This phenomenon has been seen in the increasing detection of cytomegalovirus (CMV) in mucocutaneous swabs for herpesviruses, the microbiological significance of which is a priori unclear. The aim of our study was to determine if an incidental finding of a positive CMV result represented CMV disease, if it facilitated a timely diagnosis of CMV disease or whether there were any deleterious outcomes. We performed a retrospective review of patients with an incidentally positive PCR result for CMV on external and mucosal swabs, including medical comorbidities and presence of immunosuppression, subsequent investigations, whether a diagnosis of CMV disease was made, and treatment. CMV detection was infrequent, detected in 158 (3.4%) of 4626 herpes multiplex PCR tests performed. The majority (60.4%) of patients were immunocompromised, and amongst these patients a positive swab represented a new diagnosis or already known CMV disease in 14%. In seven patients (5%), all of whom were immunocompromised, the positive CMV PCR on a swab led to further investigation and subsequent diagnosis and treatment of CMV disease. Whilst not recommended for diagnosis of CMV disease, if CMV is detected on a mucocutaneous swab in an immunocompromised patient, further assessment and investigation for CMV disease should be undertaken.Copyright © 2020 Royal College of Pathologists of Australasiaen
dc.languageenen
dc.languageEnglishen
dc.publisherElsevier B.V.en
dc.relation.ispartofPathologyen
dc.subject.meshaged-
dc.subject.meshbullous pemphigoid-
dc.subject.meshcancer combination chemotherapy-
dc.subject.meshCytomegalovirus-
dc.subject.meshcytomegalovirus infection-
dc.subject.meshdiagnostic test accuracy study-
dc.subject.meshdiffuse large B cell lymphoma-
dc.subject.meshimmunocompromised patient-
dc.subject.meshimmunosuppressive treatment-
dc.subject.meshincidental finding-
dc.subject.meshinfant-
dc.subject.meshliver failure-
dc.subject.meshliver failure [Surgery]-
dc.subject.meshliver transplantation-
dc.subject.meshlupus erythematosus nephritis-
dc.subject.meshmedical record-
dc.subject.meshmouth ulcer-
dc.subject.meshmucus-
dc.subject.meshmultiplex polymerase chain reaction-
dc.subject.meshnewborn-
dc.subject.meshpalliative therapy-
dc.subject.meshpathologist-
dc.subject.meshpemphigus vulgaris-
dc.subject.meshrheumatoid arthritis-
dc.subject.meshschool child-
dc.subject.meshprednisolone-
dc.subject.meshvalganciclovir-
dc.subject.meshpolymerase chain reaction system-
dc.subject.meshmucosal swab-
dc.subject.mesh2012-15 AusDiagnostics Easy-Plex 12-well assay-
dc.subject.mesh2015-16 AusDiagnostics High-Plex Herpes, Enterovirus and Adenovirus 16-well assay-
dc.subject.meshantiviral therapy-
dc.subject.meshskin biopsy-
dc.subject.meshskin injury-
dc.subject.meshsmear-
dc.subject.meshstatistically significant result-
dc.subject.meshsystemic disease-
dc.subject.meshT cell lymphoma-
dc.subject.meshvery elderly-
dc.subject.meshvirus detection-
dc.subject.meshazathioprine-
dc.subject.meshmycophenolic acid-
dc.subject.meshcyclophosphamide plus doxorubicin plus etoposide plus prednisolone plus rituximab plus vincristine-
dc.subject.meshcyclophosphamide plus doxorubicin plus prednisolone plus rituximab plus vincristine-
dc.subject.meshganciclovir-
dc.subject.meshmethotrexate-
dc.titleIncidental mucocutaneous cytomegalovirus detection and its predictive value for systemic disease.en
dc.typeArticleen
dc.identifier.affiliationInfectious Diseases and Clinical Microbiology-
dc.identifier.affiliationPathology-
dc.identifier.affiliationInfectious Diseases and Clinical Microbiology-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.pathol.2020.02.009-
dc.publisher.placeUnited Statesen
dc.identifier.pubmedid32354659 [http://www.ncbi.nlm.nih.gov/pubmed/?term=32354659]en
dc.identifier.source2005700745en
dc.identifier.institution(Hughes, Spring, Radalage, Graham, Dendle, Rogers) Monash Infectious Diseases, Monash Medical Centre, Monash Health, Clayton, Victoria, Australia (Hughes, Graham) Department of Microbiology, Monash Pathology, Monash Health, Clayton, Victoria, Australia (Dendle, Rogers) Centre for Inflammatory Diseases, Monash University, Melbourne, Victoria, Australiaen
dc.description.addressC.M. Hughes, c/o Monash Infectious Diseases, Monash Medical Centre, 246 Clayton Road, Clayton, Vic 3168, Australia. E-mail: carly_m_hughes@yahoo.com.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2020 Elsevier B.V., All rights reserved.en
dc.subect.keywordsCytomegalovirus immunocompromised hosten
dc.identifier.authoremailHughes C.M.; carly_m_hughes@yahoo.com.auen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.openairetypeArticle-
crisitem.author.deptInfection Prevention and Epidemiology-
crisitem.author.deptInfectious Diseases and Clinical Microbiology-
crisitem.author.deptInfectious Diseases and Clinical Microbiology-
crisitem.author.deptInfectious Diseases and Clinical Microbiology-
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