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https://dora.health.qld.gov.au/qldresearchjspui/handle/1/5705
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DC Field | Value | Language |
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dc.contributor.author | Forde, Brian M. | - |
dc.contributor.author | Bergh, Haakon | - |
dc.contributor.author | Cuddihy, Thom | - |
dc.contributor.author | Hajkowicz, Krispin | - |
dc.contributor.author | Hurst, Trish | - |
dc.contributor.author | Playford, E. Geoffrey | - |
dc.contributor.author | Henderson, Belinda C. | - |
dc.contributor.author | Runnegar, Naomi | - |
dc.contributor.author | Clark, Julia | - |
dc.contributor.author | Jennison, Amy V. | - |
dc.contributor.author | Moss, Susan | - |
dc.contributor.author | Hume, Anna | - |
dc.contributor.author | Leroux, Hugo | - |
dc.contributor.author | Beatson, Scott A. | - |
dc.contributor.author | Paterson, David L. | - |
dc.contributor.author | Harris, Patrick N. A. | - |
dc.date.accessioned | 2024-06-20T00:27:04Z | - |
dc.date.available | 2024-06-20T00:27:04Z | - |
dc.date.issued | 2023 | - |
dc.identifier.citation | Clinical Infectious Diseases, 2023 (76) 3 p.e1277-e1284 | en |
dc.identifier.uri | https://dora.health.qld.gov.au/qldresearchjspui/handle/1/5705 | - |
dc.description.abstract | Background Prospective whole-genome sequencing (WGS)-based surveillance may be the optimal approach to rapidly identify transmission of multi-drug resistant (MDR) bacteria in the healthcare setting. Methods We prospectively collected methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant enterococci (VRE), carbapenem-resistant Acinetobacter baumannii (CRAB), extended-spectrum beta-lactamase (ESBL-E), and carbapenemase-producing Enterobacterales (CPE) isolated from blood cultures, sterile sites, or screening specimens across three large tertiary referral hospitals (2 adult, 1 paediatric) in Brisbane, Australia. WGS was used to determine in silico multi-locus sequence typing (MLST) and resistance gene profiling via a bespoke genomic analysis pipeline. Putative transmission events were identified by comparison of core genome single nucleotide polymorphisms (SNPs). Relevant clinical meta-data were combined with genomic analyses via customised automation, collated into hospital-specific reports regularly distributed to infection control teams. Results Over 4 years (April 2017 to July 2021) 2660 isolates were sequenced. This included MDR gram-negative bacilli (n = 293 CPE, n = 1309 ESBL), MRSA (n = 620), and VRE (n = 433). A total of 379 clinical reports were issued. Core genome SNP data identified that 33% of isolates formed 76 distinct clusters. Of the 76 clusters, 43 were contained to the 3 target hospitals, suggesting ongoing transmission within the clinical environment. The remaining 33 clusters represented possible inter-hospital transmission events or strains circulating in the community. In 1 hospital, proven negligible transmission of non-multi-resistant MRSA enabled changes to infection control policy. Conclusions Implementation of routine WGS for MDR pathogens in clinical laboratories is feasible and can enable targeted infection prevention and control interventions. | - |
dc.title | Clinical Implementation of Routine Whole-genome Sequencing for Hospital Infection Control of Multi-drug Resistant Pathogens | - |
dc.identifier.doi | 10.1093/cid/ciac726 | - |
dc.relation.url | https://search.ebscohost.com/login.aspx?direct=true&AuthType=ip,athens&db=ccm&AN=161829825&site=ehost-live | - |
dc.identifier.journaltitle | Clinical Infectious Diseases | - |
dc.identifier.risid | 4406 | - |
dc.description.pages | e1277-e1284 | - |
dc.description.volume | 76 | - |
dc.description.issue | 3 | - |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
Appears in Sites: | Children's Health Queensland Publications |
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