Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30058
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dc.contributor.authorSherry, Norelle L-
dc.contributor.authorGorrie, Claire L-
dc.contributor.authorKwong, Jason C-
dc.contributor.authorHiggs, Charlie-
dc.contributor.authorStuart, Rhonda L-
dc.contributor.authorMarshall, Caroline-
dc.contributor.authorBallard, Susan A-
dc.contributor.authorSait, Michelle-
dc.contributor.authorKorman, Tony M-
dc.contributor.authorSlavin, Monica A-
dc.contributor.authorLee, Robyn S-
dc.contributor.authorGraham, Maryza-
dc.contributor.authorLeroi, Marcel J-
dc.contributor.authorWorth, Leon J-
dc.contributor.authorChan, Hiu Tat-
dc.contributor.authorSeemann, Torsten-
dc.contributor.authorGrayson, M Lindsay-
dc.contributor.authorHowden, Benjamin P-
dc.date2022-06-
dc.date.accessioned2022-06-22T06:51:21Z-
dc.date.available2022-06-22T06:51:21Z-
dc.date.issued2022-04-12-
dc.identifier.citationThe Lancet Regional Health. Western Pacific 2022; 23: 100446en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/30058-
dc.description.abstractCurrent microbiological methods lack the resolution to accurately identify multidrug-resistant organism (MDRO) transmission, however, whole genome sequencing can identify highly-related patient isolates providing opportunities for precision infection control interventions. We investigated the feasibility and potential impact of a prospective multi-centre genomics workflow for hospital infection control. We conducted a prospective genomics implementation study across eight Australian hospitals over 15 months (2017,2018), collecting all clinical and screening isolates from inpatients with vanA VRE, MRSA, ESBL Escherichia coli (ESBL-Ec), or ESBL Klebsiella pneumoniae (ESBL-Kp). Genomic and epidemiologic data were integrated to assess MDRO transmission. In total, 2275 isolates were included from 1970 patients, predominantly ESBL-Ec (40·8%) followed by MRSA (35·6%), vanA VRE (15·2%), and ESBL-Kp (8·3%).Overall, hospital and genomic epidemiology showed 607 patients (30·8%) acquired their MDRO in hospital, including the majority of vanA VRE (266 patients, 86·4%), with lower proportions of ESBL-Ec (186 patients, 23·0%), ESBL-Kp (42 patients, 26·3%), and MRSA (113 patients, 16·3%). Complex patient movements meant the majority of MDRO transmissions would remain undetected without genomic data.The genomics implementation had major impacts, identifying unexpected MDRO transmissions prompting new infection control interventions, and contributing to vanA VRE becoming a notifiable condition. We identified barriers to implementation and recommend strategies for mitigation. Implementation of a multi-centre genomics-informed infection control workflow is feasible and identifies many unrecognised MDRO transmissions. This provides critical opportunities for interventions to improve patient safety in hospitals. Melbourne Genomics Health Alliance (supported by State Government of Victoria, Australia), and National Health and Medical Research Council (Australia).en
dc.language.isoeng
dc.subjectAntimicrobial resistanceen
dc.subjectESBL-Ec, Extended-spectrum beta-lactamase Escherichia colien
dc.subjectESBL-Kp, Extended-spectrum beta-lactamase Klebsiella pneumoniaeen
dc.subjectHospital epidemiologyen
dc.subjectInfection prevention and controlen
dc.subjectMDRO, Multidrug-resistant organismen
dc.subjectMRSA, Methicillin-resistant Staphylococcus aureusen
dc.subjectVRE, Vancomycin-resistant Enterococcusen
dc.subjectWGS, Whole genome sequencingen
dc.subjectWhole genome sequencingen
dc.titleMulti-site implementation of whole genome sequencing for hospital infection control: A prospective genomic epidemiological analysis.en
dc.typeJournal Articleen
dc.identifier.journaltitleThe Lancet Regional Health. Western Pacificen
dc.identifier.affiliationMicrobiologyen
dc.identifier.affiliationDepartment of Infectious Diseases, Peter MacCallum Cancer Centre, Parkville, Victoria, Australia..en
dc.identifier.affiliationNational Centre for Infections in Cancer, Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Victoria, Australia..en
dc.identifier.affiliationInfectious Diseasesen
dc.identifier.affiliationDepartment of Microbiology & Immunology at the Peter Doherty Institute for Infection & Immunity, University of Melbourne, Melbourne, Victoria, Australia..en
dc.identifier.affiliationMedicine (University of Melbourne)en
dc.identifier.affiliationMonash Infectious Diseases, Monash Health, Clayton, Victoria, Australia..en
dc.identifier.affiliationMonash University, Clayton, Victoria, Australia..en
dc.identifier.affiliationSouth East Public Health Unit, Monash Health, Clayton, Victoria, Australia..en
dc.identifier.affiliationMicrobiological Diagnostic Unit (MDU) Public Health Laboratory, Department of Microbiology & Immunology at the Peter Doherty Institute for Infection & Immunity, University of Melbourne, Melbourne, Victoria, Australia..en
dc.identifier.affiliationDepartment of Microbiology, Melbourne Health, Parkville, Victoria, Australia..en
dc.identifier.affiliationInfection Prevention & Surveillance, Victorian Infectious Diseases Service, Melbourne Health, Parkville, Victoria, Australia..en
dc.identifier.affiliationDepartment of Infectious Diseases, The University of Melbourne at the Peter Doherty Institute for Infection & Immunity, Melbourne, Victoria, Australia..en
dc.identifier.affiliationDepartment of Microbiology, Monash Health, Clayton, Victoria, Australia..en
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35465046/en
dc.identifier.doi10.1016/j.lanwpc.2022.100446en
dc.type.contentTexten
dc.identifier.orcid0000-0002-7789-8360en
dc.identifier.orcid0000-0002-6298-7942en
dc.identifier.orcid0000-0002-2659-7728en
dc.identifier.orcid0000-0002-3261-3149en
dc.identifier.orcid0000-0003-0237-1473en
dc.identifier.pubmedid35465046
local.name.researcherGrayson, M Lindsay
item.grantfulltextnone-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptMicrobiology-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptMicrobiology-
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