Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/23829
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dc.contributor.authorLane, Courtney R-
dc.contributor.authorBrett, Judith-
dc.contributor.authorSchultz, Mark-
dc.contributor.authorGorrie, Claire L-
dc.contributor.authorStevens, Kerrie-
dc.contributor.authorCameron, Donna R M-
dc.contributor.authorSt George, Siobhan-
dc.contributor.authorvan Diemen, Annaliese-
dc.contributor.authorEaston, Marion-
dc.contributor.authorStuart, Rhonda L-
dc.contributor.authorSait, Michelle-
dc.contributor.authorPeleg, Anton Y-
dc.contributor.authorStewardson, Andrew J-
dc.contributor.authorCheng, Allen C-
dc.contributor.authorSpelman, Denis W-
dc.contributor.authorWaters, Mary Jo-
dc.contributor.authorBallard, Susan A-
dc.contributor.authorSherry, Norelle L-
dc.contributor.authorWilliamson, Deborah A-
dc.contributor.authorRomanes, Finn-
dc.contributor.authorSutton, Brett-
dc.contributor.authorKwong, Jason C-
dc.contributor.authorSeemann, Torsten-
dc.contributor.authorGoncalves da Silva, Anders-
dc.contributor.authorStephens, Nicola-
dc.contributor.authorHowden, Benjamin P-
dc.date2020-07-14-
dc.date.accessioned2020-07-16T03:31:43Z-
dc.date.available2020-07-16T03:31:43Z-
dc.date.issued2021-
dc.identifier.citationClinical infectious diseases : an official publication of the Infectious Diseases Society of America 2021; 73(11): e3912-e3920-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/23829-
dc.description.abstractMulti-resistant organisms (MROs) pose a critical threat to public health. Population-based programs for control of MROs such as Carbapenemase-producing Enterobacterales (CPE) have emerged and evaluation is needed. We assess the feasibility and impact of a state-wide CPE surveillance and response program deployed in December 2015 across Victoria, Australia (population 6.5 million). A prospective multi-modal intervention including active screening, carrier isolation, centralised case investigation and comparative pathogen genomics was implemented. We analyze trend in CPE incidence and clinical presentation, risk factors and local transmission over the program's first three years (January 2016 to December 2018). CPE case ascertainment increased over the study period to 1.42 cases/100,000 population, linked to increased screening without a concomitant rise in active clinical infections (0.45-0.60 infections/100,000 population, p=0.640). KPC-2 infection decreased from 0.29 infections/100,000 population prior to intervention to 0.03 infections/100,000 population in 2018 (p=0.003). Comprehensive case investigation identified putative overseas community acquisition. Median time between isolate referral and initial genomic and epidemiological assessment for local transmission was 11 days (IQR 9-14). Prospective surveillance identified numerous small transmission networks (median 2, range 1-19 cases), predominantly IMP and KPC, with median pairwise distance of 8 (IQR 4-13) single nucleotide polymorphisms; low diversity between clusters of the same sequence type suggested genomic cluster definitions alone are insufficient for targeted response. We demonstrate the value of centralised CPE control programs to increase case ascertainment, resolve risk factors and identify putative local transmission through prospective genomic and epidemiological surveillance; methodologies are transferable to low-prevalence settings and MROs globally.-
dc.language.isoeng-
dc.subjectAntimicrobial resistance-
dc.subjectCarbapenemase producing Enterobacterales-
dc.subjectPublic Health Surveillance-
dc.subjectgenomics-
dc.subjectinfection control-
dc.titleSearch and Contain: Impact of an integrated genomic and epidemiological surveillance and response program for control of carbapenemase-producing Enterobacterales.-
dc.typeJournal Article-
dc.identifier.journaltitleClinical Infectious Diseases-
dc.identifier.affiliationVICNISS Healthcare Associated Infection Surveillance Coordinating Centre, at the Peter Doherty Institute for Infection & Immunity, Melbourne, Victoria, Australiaen
dc.identifier.affiliationInfection and Immunity Program, Monash Biomedicine Discovery Institute, Department of Microbiology, Monash University, Innovation Walk, Clayton, Victoria, Australiaen
dc.identifier.affiliationMonash Infectious Diseases, Monash Health, Monash Medical Centre, Clayton, Victoria, Australiaen
dc.identifier.affiliationDepartment of Health and Human Services, Melbourne, Victoria, Australiaen
dc.identifier.affiliationMicrobiological Diagnostic Unit Public Health Laboratory, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Microbiology & Immunology, The University of Melbourne at the Peter Doherty Institute for Infection & Immunity , Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Infectious Diseases, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationUniversity of Tasmania, Medical Science Precinct, Hobart, Tasmania, Australiaen
dc.identifier.affiliationDepartment of Microbiology, St Vincent's Hospital Melbourne, Victoria Parade, Fitzroy, Victoria, Australiaen
dc.identifier.affiliationDepartment of Infectious Diseases, Alfred Hospital, and Central Clinical School, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.affiliationDepartment of Microbiology, The Alfred Hospital, Melbourne, Victoria, Australiaen
dc.identifier.affiliationSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australiaen
dc.identifier.doi10.1093/cid/ciaa972-
dc.identifier.orcid0000-0002-7789-8360-
dc.identifier.pubmedid32663248-
dc.type.austinJournal Article-
local.name.researcherHowden, Benjamin P
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptMicrobiology-
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