A retrospective observational cohort study of the clinical epidemiology of bloodstream infections due to carbapenem-resistant Klebsiella pneumoniae in an OXA-48 endemic setting
dc.authorid | Tanriverdi, Elif Seren/0000-0002-0449-0356 | |
dc.authorid | Bilir, Yeliz/0000-0003-2217-4741 | |
dc.authorid | AKYON YILMAZ, YAKUT/0000-0002-0919-5508 | |
dc.authorid | Otlu, Baris/0000-0002-6220-0521 | |
dc.authorid | Tozluyurt, Abdullah/0000-0001-7036-0587 | |
dc.authorwosid | Kırbaş, Ekin/KFA-9949-2024 | |
dc.authorwosid | Dag, Osman/S-5379-2016 | |
dc.authorwosid | Tanriverdi, Elif Seren/ABE-4472-2021 | |
dc.authorwosid | Aslan, Abdullah Tarık/AAP-8774-2021 | |
dc.authorwosid | Bilir, Yeliz/GPG-1602-2022 | |
dc.authorwosid | AKYON YILMAZ, YAKUT/HJI-0282-2023 | |
dc.contributor.author | Aslan, Abdullah Tarik | |
dc.contributor.author | Kirbas, Ekin | |
dc.contributor.author | Sancak, Banu | |
dc.contributor.author | Tanriverdi, Elif Seren | |
dc.contributor.author | Otlu, Baris | |
dc.contributor.author | Gursoy, Nafia Canan | |
dc.contributor.author | Yilmaz, Yakut Akyon | |
dc.date.accessioned | 2024-08-04T20:51:49Z | |
dc.date.available | 2024-08-04T20:51:49Z | |
dc.date.issued | 2022 | |
dc.department | İnönü Üniversitesi | en_US |
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. | en_US |
dc.description.sponsorship | Hacettepe University Scientific Research Council [THD-18711]; Pfizer [PF-06416494, WI247317] | en_US |
dc.description.sponsorship | This study was supported by Hacettepe University Scientific Research Council (Grant No. THD-18711). Furthermore, Pfizer provided 1 g avibactam-sodium powder (PF-06416494) as a compound transfer agreement grant (Grant No. WI247317). Hacettepe University Scientific Research Council and Pfizer had no role in the design and execution of the study, collection, management, analysis and interpretation of the data; preparation, review or approval of the manuscript; nor the decision to submit the manuscript for publication, veto publication, or to control the journal to which this paper was submitted. | en_US |
dc.identifier.doi | 10.1016/j.ijantimicag.2022.106554 | |
dc.identifier.issn | 0924-8579 | |
dc.identifier.issn | 1872-7913 | |
dc.identifier.issue | 4 | en_US |
dc.identifier.pmid | 35176476 | en_US |
dc.identifier.scopus | 2-s2.0-85127366976 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.ijantimicag.2022.106554 | |
dc.identifier.uri | https://hdl.handle.net/11616/100578 | |
dc.identifier.volume | 59 | en_US |
dc.identifier.wos | WOS:000821489800006 | en_US |
dc.identifier.wosquality | Q1 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartof | International Journal of Antimicrobial Agents | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Carbapenem-resistant Klebsiella pneumoniae | en_US |
dc.subject | Mortality | en_US |
dc.subject | OXA-48-like | en_US |
dc.subject | Treatment | en_US |
dc.subject | Carbapenemase | en_US |
dc.title | A retrospective observational cohort study of the clinical epidemiology of bloodstream infections due to carbapenem-resistant Klebsiella pneumoniae in an OXA-48 endemic setting | en_US |
dc.type | Article | en_US |