Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/6592
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dc.contributor.authorTabah, A.en
dc.contributor.authorEdwards, F.en
dc.contributor.authorRamanan, M.en
dc.contributor.authorWhite, K. C.en
dc.contributor.authorShekar, K.en
dc.contributor.authorMcIlroy, P.en
dc.contributor.authorAttokaran, A.en
dc.contributor.authorSenthuran, S.en
dc.contributor.authorMcCullough, J.en
dc.contributor.authorKumar, A.en
dc.contributor.authorLuke, S.en
dc.contributor.authorBhadange, N.en
dc.contributor.authorGarrett, P.en
dc.contributor.authorLaupland, K. B.en
dc.date.accessioned2025-03-12T03:06:17Z-
dc.date.available2025-03-12T03:06:17Z-
dc.date.issued2024-
dc.identifier.citationIntensive care unit–onset bloodstream infections represent a distinct category of hospital–onset infections: A multicentre, retrospective cohort study. Queensland Critical Care Network (QCCRN) Alexis Tabah, Felicity Edwards, Mahesh Ramanan, Kyle C White, Kiran Shekar, Philippa McIlroy, Antony Attokaran, Siva Senthuran, James McCullough, Aashish Kumar, Stephen Luke, Neeraj Bhadange, Peter Garrett, and Kevin B Laupland Journal of the Association of Medical Microbiology and Infectious Disease Canada 2024 9:4, 229-238en
dc.identifier.urihttps://dora.health.qld.gov.au/qldresearchjspui/handle/1/6592-
dc.descriptionCairns & Hinterland Hospital and Health Service (CHHHS) affiliated author: Philippa McIlroyen
dc.description.abstractBackground: The location of onset of bloodstream infections (BSIs) associated with intensive care unit (ICU) admission may influence their clinical and epidemiological characteristics. Methods: A multicentre, retrospective cohort study was conducted in Queensland, Australia, and BSIs associated with ICU admission were identified and classified as community-onset, hospital-onset, or ICU-onset if first isolated within, after 48 hours but within 48 hours of ICU admission, or after 48 hours following ICU admission, respectively. Results: We included 3,540 episodes of ICU-associated BSI, with 1,693 classified as community-onset, 663 hospital-onset, and 1,184 ICU-onset. Compared with hospital-onset BSIs, patients with ICU-onset BSIs were younger, had fewer comorbidities, had lower APACHE II scores, and were more likely male. Patients with ICU-onset BSI were more likely to be surgical admissions and have a primary cardiovascular or neurological diagnosis. The distribution of infective agents varied significantly among community-, hospital-, and ICU-onset BSI groups. The all-cause 30-day case-fatality rates for first-episode community-onset, hospital-onset, and ICU-onset BSIs were 17.1%, 21.7%, and 23.5%, respectively (p < 0.001). Conclusion: With different epidemiological features and causal pathogens, ICU-onset BSI represents a distinct BSI group arising in hospitalized patients.en
dc.language.isoenen
dc.relation.ispartofJournal of the Association of Medical Microbiology and Infectious Disease Canadaen
dc.subjectbloodborne infectionsen
dc.subjectepidemiologyen
dc.subjectinfection controlen
dc.subjectsepsisen
dc.titleIntensive care unit–onset bloodstream infections represent a distinct category of hospital–onset infections: A multicentre, retrospective cohort study. Queensland Critical Care Network (QCCRN)en
dc.typeArticleen
dc.identifier.doi10.3138/jammi-2024-002-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.fulltextWith Fulltext-
item.languageiso639-1en-
Appears in Sites:Cairns & Hinterland HHS Publications
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