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Australian Group on Antimicrobial Resistance Australian Staphylococcus aureus Sepsis Outcome Programme annual report, 2014

dc.contributor.authorCoombs, Geoffrey W
dc.contributor.authorDaley, Denise A
dc.contributor.authorThin Lee, Yung
dc.contributor.authorPearson, Julie
dc.contributor.authorRobinson, J. Owen
dc.contributor.authorNimmo, G.R.
dc.contributor.authorCollignon, Peter
dc.contributor.authorHowden, Benjamin
dc.contributor.authorBell, Jan M.
dc.contributor.authorTurnidge, John D
dc.date.accessioned2022-06-06T04:49:49Z
dc.date.issued2016
dc.date.updated2021-01-17T07:18:08Z
dc.description.abstractFrom 1 January to 31 December 2014, 27 institutions around Australia participated in the Australian Staphylococcal Sepsis Outcome Programme (ASSOP). The aim of ASSOP 2014 was to determine the proportion of Staphylococcus aureus bacteraemia (SAB) isolates in Australia that are antimicrobial resistant, with particular emphasis on susceptibility to methicillin and to characterise the molecular epidemiology of the isolates. Overall, 18.8% of the 2,206 SAB episodes were methicillin resistant, which was significantly higher than that reported in most European countries. The 30-day all-cause mortality associated with methicillin-resistant SAB was 23.4%, which was significantly higher than the 14.4% mortality associated with methicillin-sensitive SAB (P <0.0001). With the exception of the beta-lactams and erythromycin, antimicrobial resistance in methicillin-sensitive S. aureus remains rare. However in addition to the beta-lactams, approximately 50% of methicillin-resistant S. aureus (MRSA) were resistant to erythromycin and ciprofloxacin and approximately 15% were resistant to co-trimoxazole, tetracycline and gentamicin. When applying the European Committee on Antimicrobial Susceptibility Testing breakpoints, teicoplanin resistance was detected in 2 S. aureus isolates. Resistance was not detected for vancomycin or linezolid. Resistance to non-beta-lactam antimicrobials was largely attributable to 2 healthcare-associated MRSA clones; ST22-IV [2B] (EMRSA-15) and ST239-III [3A] (Aus-2/3 EMRSA). ST22-IV [2B] (EMRSA-15) has become the predominant healthcare associated clone in Australia. Sixty per cent of methicillin-resistant SAB were due to community-associated (CA) clones. Although polyclonal, almost 44% of community-associated clones were characterised as ST93-IV [2B] (Queensland CA-MRSA) and ST1-IV [2B] (WA1). CA-MRSA, in particular the ST45-V [5C2&5] (WA84) clone, has acquired multiple antimicrobial resistance determinants including ciprofloxacin, erythromycin, clindamycin, gentamicin and tetracycline. As CA-MRSA is well established in the Australian community it is important that antimicrobial resistance patterns in community and healthcare-associated SAB is monitored as this information will guide therapeutic practices in treating S. aureus sepsis.en_AU
dc.description.sponsorshipThis study was primarily funded by a grant from the Australian Government Department of Health. We gratefully acknowledge Yung Ching Lee from the Department of Microbiology, PathWest Laboratory Medicine – WA, Fiona Stanley Hospital.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1447-4514en_AU
dc.identifier.urihttp://hdl.handle.net/1885/267153
dc.language.isoen_AUen_AU
dc.publisherAustralian Government. Department of Health and Ageing. Office of Health Protection, Surveillance Branchen_AU
dc.rights© 2016 The authorsen_AU
dc.sourceCommunicable Diseases Intelligence Quarterly Reporten_AU
dc.subjectAustralian Group on Antimicrobial Resistanceen_AU
dc.subjectantimicrobial resistance surveillanceen_AU
dc.subjectStaphylococcus aureusen_AU
dc.subjectmethicillin sensitiveen_AU
dc.subjectmethicillin resistanten_AU
dc.subjectbacteraemiaen_AU
dc.titleAustralian Group on Antimicrobial Resistance Australian Staphylococcus aureus Sepsis Outcome Programme annual report, 2014en_AU
dc.typeJournal articleen_AU
local.bibliographicCitation.issue2en_AU
local.bibliographicCitation.lastpageE254en_AU
local.bibliographicCitation.startpageE244en_AU
local.contributor.affiliationCoombs, Geoffrey W, PathWest Laboratory Medicineen_AU
local.contributor.affiliationDaley, Denise A, Royal Perth Hospital, Australian Group on Antimicrobial Resistanceen_AU
local.contributor.affiliationThin Lee, Yung, Murdoch Universityen_AU
local.contributor.affiliationPearson, Julie, PathWest Laboratory Medicineen_AU
local.contributor.affiliationRobinson, J. Owen, Murdoch Universityen_AU
local.contributor.affiliationNimmo, G.R., Pathology Queensland Central Laboratoryen_AU
local.contributor.affiliationCollignon, Peter, College of Health and Medicine, ANUen_AU
local.contributor.affiliationHowden, Benjamin, University of Melbourneen_AU
local.contributor.affiliationBell, Jan M., Women’s and Children’s Hospitalen_AU
local.contributor.affiliationTurnidge, John D, Women's and Children's Hospitalen_AU
local.contributor.authoruidCollignon, Peter, u1845890en_AU
local.description.embargo2099-12-31
local.description.notesImported from ARIESen_AU
local.identifier.absfor111708 - Health and Community Servicesen_AU
local.identifier.absseo920299 - Health and Support Services not elsewhere classifieden_AU
local.identifier.ariespublicationa383154xPUB12774en_AU
local.identifier.ariespublicationu5436353xPUB18
local.identifier.citationvolume40en_AU
local.identifier.scopusID2-s2.0-85012009776
local.publisher.urlhttps://www1.health.gov.au/en_AU
local.type.statusPublished Versionen_AU

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