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dc.contributor.authorAlıcı A.
dc.contributor.authorÇetin Ş.
dc.contributor.authorÇetin M.
dc.contributor.authorDörtok H.
dc.date.accessioned2024-03-12T19:35:45Z
dc.date.available2024-03-12T19:35:45Z
dc.date.issued2023
dc.identifier.issn1301143X
dc.identifier.urihttps://doi.org/10.36519/kd.2023.4706
dc.identifier.urihttps://hdl.handle.net/20.500.12450/2985
dc.description.abstractIntroduction: Inflammatory indicators such as procalcitonin (PCT) and C-reactive protein (CRP) may vary depend-ing on the etiology of bloodstream infections. In this study, we aimed to investigate the role of serum PCT and CRP levels in predicting etiology in bloodstream infections. Methods: Blood cultures sent to our hospital’s microbiology laboratory between January 2018 and July 2021 were retrospectively evaluated, and 501 patients with positive blood cultures were included in the study. According to blood culture growth, the patients were divided into Gram-negative bacteria (GNB), Gram-positive bacteria (GPB), fungus, Enterobacterales, and non-fermenter groups. We investigated whether there was a significant difference in the PCT and CRP values between the groups. Student’s t-test was used to compare normally distributed numerical data, and the Mann-Whitney U test was used to compare non-normally distributed numerical data. The median value for continuous variables in each group was given as the first quartile (Q1) and third quartile (Q3). A comparison of cat-egorical data was done with ?2 test. Results: The PCT median value was found to be significantly higher in the GNB group compared with the GNB-GPB group. There was no significant difference between any of the groups for the CRP median value. In the GNB-GPB group comparison, the area under the curve for PCT cut-off value of 0.5 ng/mL was found to be 0.675 in the ROC curve (95% confidence interval=0.623-0.726; p<0.001), and the optimal cut-off value was found to be 1.45 ng/mL with 75% sensitivity, 53% specificity. Conclusions: Procalcitonin was found to be a marker that can be used to differentiate Gram-negative bacteremia from Gram-positive bacteremia. We concluded that CRP cannot be used to predict the etiology of bacteremia. © 2023, DOC Design and Informatics Co. Ltd.. All rights reserved.en_US
dc.language.isoturen_US
dc.publisherDOC Design and Informatics Co. Ltd.en_US
dc.relation.ispartofKlimik Dergisien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectbloodstream infectionen_US
dc.subjectC-reactive proteinen_US
dc.subjectprocalcitoninen_US
dc.subjectC reactive proteinen_US
dc.subjectprocalcitoninen_US
dc.subjectarea under the curveen_US
dc.subjectArticleen_US
dc.subjectblood cultureen_US
dc.subjectbloodstream infectionen_US
dc.subjectcontrolled studyen_US
dc.subjectdiagnostic test accuracy studyen_US
dc.subjectEnterobacteralesen_US
dc.subjectGram negative bacteriumen_US
dc.subjectGram positive bacteriumen_US
dc.subjecthumanen_US
dc.subjectmajor clinical studyen_US
dc.subjectsensitivity and specificityen_US
dc.titleThe Role of Procalcitonin and C-Reactive Protein in Prediction of Etiology of Bloodstream Infectionsen_US
dc.title.alternativeKan Dolaşımı İnfeksiyonlarının Etiyolojisini Tahmin Etmede Prokalsitonin ve C-Reaktif Proteinin Rolüen_US
dc.typearticleen_US
dc.departmentAmasya Üniversitesien_US
dc.identifier.volume36en_US
dc.identifier.issue4en_US
dc.identifier.startpage268en_US
dc.identifier.endpage273en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-85181216620en_US
dc.identifier.doi10.36519/kd.2023.4706
dc.department-tempAlıcı, A., Tatvan Devlet Hastanesi, Tıbbi Mikrobiyoloji Kliniği, Bitlis, Turkey; Çetin, Ş., Amasya Üniversitesi Tıp Fakültesi, Biyoistatistik Anabilim Dalı, Amasya, Turkey; Çetin, M., Amasya Üniversitesi Tıp Fakültesi, Tıbbi Mikrobiyoloji Anabilim Dalı, Amasya, Turkey; Dörtok, H., Amasya Üniversitesi Tıp Fakültesi, Tıbbi Biyokimya Anabilim Dalı, Amasya, Turkeyen_US
dc.authorscopusid58185618000
dc.authorscopusid57196121521
dc.authorscopusid18036804900
dc.authorscopusid58790752000


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