Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/27554
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dc.contributor.authorHowden B.P.en
dc.contributor.authorAnderson T.L.en
dc.contributor.authorRoberts S.A.en
dc.contributor.authorWarren S.J.C.en
dc.contributor.authorGao W.en
dc.contributor.authorJohnson P.D.R.en
dc.contributor.authorHolmes N.E.en
dc.contributor.authorTurnidge J.D.en
dc.contributor.authorMunckhof W.J.en
dc.contributor.authorRobinson J.O.en
dc.contributor.authorKorman T.en
dc.contributor.authorO'Sullivan M.V.N.en
dc.date.accessioned2021-05-14T09:16:41Zen
dc.date.available2021-05-14T09:16:41Zen
dc.date.copyright2013en
dc.date.created20130328en
dc.date.issued2013-03-28en
dc.identifier.citationAntimicrobial Agents and Chemotherapy. 57 (4) (pp 1654-1663), 2013. Date of Publication: April 2013.en
dc.identifier.issn0066-4804en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/27554en
dc.description.abstractA ratio of the vancomycin area under the concentration-time curve to the MIC (AUC/MIC) of >= 400 has been associated with clinical success when treating Staphylococcus aureus pneumonia, and this target was recommended by recently published vancomycin therapeutic monitoring consensus guidelines for treating all serious S. aureus infections. Here, vancomycin serum trough levels and vancomycin AUC/MIC were evaluated in a "real-world" context by following a cohort of 182 patients with S. aureus bacteremia (SAB) and analyzing these parameters within the critical first 96 h of vancomycin therapy. The median vancomycin trough level at this time point was 19.5 mg/liter. There was a significant difference in vancomycin AUC/MIC when using broth microdilution (BMD) compared with Etest MIC (medians of 436.1 and 271.5, respectively; P<0.001). Obtaining the recommended vancomycin target AUC/MIC of >=400 using BMD was not associated with lower 30-day all-cause or attributable mortality from SAB (P=0.132 and P=0.273, respectively). However, an alternative vancomycin AUC/MIC of >373, derived using classification and regression tree analysis, was associated with reduced mortality (P=0.043) and remained significant in a multivariable model. This study demonstrated that we obtained vancomycin trough levels in the target therapeutic range early during the course of therapy and that obtaining a higher vancomycin AUC/MIC (in this case, >373) within 96 h was associated with reduced mortality. The MIC test method has a significant impact on vancomycin AUC/MIC estimation. Clinicians should be aware that the current target AUC/MIC of >=400 was derived using the reference BMD method, so adjustments to this target need to be made when calculating AUC/MIC ratio using other MIC testing methods. Copyright © 2013, American Society for Microbiology. All Rights Reserved.en
dc.languageEnglishen
dc.languageenen
dc.publisherAmerican Society for Microbiology (1752 N Street N.W., Washington DC 20036-2904, United States)en
dc.titleVancomycin AUC/MIC ratio and 30-day mortality in patients with Staphylococcus aureus bacteremia.en
dc.typeArticleen
dc.identifier.affiliationInfectious Diseases and Clinical Microbiology-
dc.type.studyortrialObservational study (cohort, case-control, cross sectional or survey)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1128/AAC.01485-12en
dc.publisher.placeUnited Statesen
dc.identifier.pubmedid23335735 [http://www.ncbi.nlm.nih.gov/pubmed/?term=23335735]en
dc.identifier.source368555328en
dc.identifier.institution(Holmes, Howden, Johnson) Austin Centre for Infection Research, Department of Infectious Diseases, Austin Health, Heidelberg, VIC, Australia (Holmes, Johnson) Department of Medicine, University of Melbourne, Parkville, VIC, Australia (Turnidge) SA Pathology, Women's and Children's Hospital, North Adelaide, SA, Australia (Turnidge) Department of Paediatrics, Pathology and Molecular and Biomedical Science, University of Adelaide, Adelaide, SA, Australia (Munckhof) Infection Management Services, Princess Alexandra Hospital, Woolloongabba, QLD, Australia (Munckhof) Department of Medicine, University of Queensland, St. Lucia, QLD, Australia (Robinson) Department of Infectious Diseases and Microbiology, Royal Perth Hospital, Perth, WA, Australia (Korman) Department of Infectious Diseases, Southern Health, Clayton, VIC, Australia (Korman) Department of Medicine, Monash University, Clayton, VIC, Australia (O'Sullivan) Centre for Infectious Diseases and Microbiology, Westmead Hospital, Westmead, NSW, Australia (O'Sullivan) Department of Medicine, University of Sydney, Sydney, NSW, Australia (Anderson, Warren) Department of Infectious Diseases, Royal Hobart Hospital, Hobart, TAS, Australia (Anderson, Warren) Department of Medicine, University of Tasmania, Hobart, TAS, Australia (Roberts) Auckland District Health Board, Auckland, New Zealand (Gao, Howden) Department of Microbiology, Austin Health, Heidelberg, VIC, Australia (Howden, Johnson) Department of Microbiology, Monash University, Clayton, VIC, Australia (Howden) Department of Microbiology and Immunology, University of Melbourne, Parkville, VIC, Australiaen
dc.description.addressN.E. Holmes, Austin Centre for Infection Research, Department of Infectious Diseases, Austin Health, Heidelberg, VIC, Australia. E-mail: natasha.holmes@austin.org.auen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2013 Elsevier B.V., All rights reserved.en
dc.identifier.authoremailHolmes N.E.; natasha.holmes@austin.org.auen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
crisitem.author.deptInfectious Diseases and Clinical Microbiology-
crisitem.author.deptPathology-
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