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A retrospective observational cohort study of the clinical epidemiology

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dc.contributor.author Aslan, AT
dc.contributor.author Kirbas, E
dc.contributor.author Sancak, B
dc.contributor.author Tanriverdi, ES
dc.contributor.author Otlu, B
dc.contributor.author Gursoy, NC
dc.contributor.author Yilmaz, YA
dc.contributor.author Tozluyurt, A
dc.contributor.author Liste, U
dc.contributor.author Bicakcigil, A
dc.contributor.author Hazirolan, G
dc.contributor.author Dag, O
dc.contributor.author Guven, GS
dc.contributor.author Akova, M
dc.date.accessioned 2023-01-02T08:12:11Z
dc.date.available 2023-01-02T08:12:11Z
dc.date.issued 2022
dc.identifier.uri http://hdl.handle.net/11616/86364
dc.description.abstract This study aimed to characterize the epidemiology and clinical outcomes of patients with bloodstream infections (BSIs) due to carbapenem-resistant Klebsiella pneumoniae (CRKP) in an OXA-48-predominant environment. This was a retrospective single-centre cohort study including all consecutive patients with CRKP BSIs treated between 1 January 2014 and 31 December 2018. Multivariate analysis, subgroup analysis and propensity-score-matched analysis were employed to analyse 30-day mortality as the primary outcome. Clinical cure at day 14 was also analysed for the whole cohort. In total, 124 patients with unique isolates met all the inclusion criteria. OXA-48 was the most common type of carbapenemase (85.5%). Inappropriate therapy was significantly associated with 30-day mortality [70.6% vs 39.7%, adjusted odds ratio (aOR) 4.65, 95% confidence interval (CI) 1.50-14.40, P=0.008] and 14-day clinical failure (78.5% vs 56.2%, aOR 3.14, 95% CI 1.09-9.02, P=0.033) in multivariate analyses. Among those treated appropriately, the 30-day mortality rates were similar in monotherapy and combination therapy arms (OR 2.85, 95% CI 0.68-11.95, P=0.15). INCREMENT CPE mortality score (aOR 1.16, 95% CI 1.01-1.33, P=0.029), sepsis at BSI onset (aOR 2.90, 95% CI 1.02-8.27, P=0.046), and inappropriate therapy (aOR 4.65, 95% CI 1.50-14.40, P= 0.008) were identified as independent risk factors for 30-day mortality. Colistin resistance in CRKP had no significant impact on 30-day mortality. These results were also confirmed in all propensity-scorematched analyses and sensitivity analyses. Appropriate regimens were associated with better clinical outcomes than inappropriate therapies for BSIs with CRKP predominantly possessing OXA-48. (c) 2022 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved.
dc.description.abstract C1 [Aslan, Abdullah Tarik; Guven, Gulay Sain] Hacettepe Univ, Dept Internal Med, Fac Med, Ankara, Turkey.
dc.description.abstract [Kirbas, Ekin; Sancak, Banu; Yilmaz, Yakut Akyon; Tozluyurt, Abdullah; Liste, Umran; Bicakcigil, Asiye; Hazirolan, Gulsen] Hacettepe Univ, Dept Med Microbiol, Fac Med, Ankara, Turkey.
dc.description.abstract [Tanriverdi, Elif Seren; Otlu, Baris; Gursoy, Nafia Canan] Inonu Univ, Turgut Ozal Med Ctr, Dept Med Microbiol, Mol Microbiol Lab,Fac Med, Malatya, Turkey.
dc.description.abstract [Dag, Osman] Hacettepe Univ, Dept Biostat, Fac Med, Ankara, Turkey.
dc.description.abstract [Akova, Murat] Hacettepe Univ, Dept Infect Dis & Clin Microbiol, Fac Med, TR-06100 Ankara, Turkey.
dc.description.abstract C3 Hacettepe University; Hacettepe University; Inonu University; Hacettepe
dc.description.abstract University; Hacettepe University
dc.source INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS
dc.title A retrospective observational cohort study of the clinical epidemiology
dc.title of bloodstream infections due to carbapenem-resistant Klebsiella
dc.title pneumoniae in an OXA-48 endemic setting


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