Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29979
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dc.date.accessioned2022-12-20T08:46:30Z-
dc.date.available2022-12-20T08:46:30Z-
dc.date.issued2019-07-
dc.identifier.citationEfe, C. vd. (2019). ''Validation of risk scoring systems in ursodeoxycholic acid-treated patients with primary biliary Cholangitis''. American Journal of Gastroenterology, 114(7), 1101-1108.en_US
dc.identifier.issn0002-9270-
dc.identifier.issn1572-0241-
dc.identifier.urihttps://doi.org/10.14309/ajg.0000000000000290-
dc.identifier.urihttps://journals.lww.com/ajg/Fulltext/2019/07000/Validation_of_Risk_Scoring_Systems_in.20.aspx-
dc.identifier.urihttp://hdl.handle.net/11452/29979-
dc.descriptionÇalışmada 36 yazar bulunmaktadır. Bu yazarlardan sadece Bursa Uludağ Üniversitesi mensuplarının girişleri yapılmıştır.tr_TR
dc.description.abstractINTRODUCTION: Risk stratification based on biochemical variables is a useful tool for monitoring ursodeoxycholic acid (UDCA)-treated patients with primary biliary cholangitis (PBC). Several UDCA response criteria and scoring systems have been proposed for risk prediction in PBC, but these have not been validated in large external cohorts. METHODS: We performed a study on data of 1746 UDCA-treated patients with PBC from 25 centers in Europe, United States, and Canada. The prognostic performance of the risk scoring systems (GLOBE and UK-PBC) and the UDCA response criteria (Barcelona, Paris I, Paris II, Rotterdam, and Toronto) were evaluated. We regarded cirrhosis-related complications (ascites, variceal bleeding, and/or hepatic encephalopathy) as clinical end points. RESULTS: A total of 171 patients reached a clinical end point during a median 7 years (range 1-16 years) of follow-up. The 5-, 10- and 15-year adverse outcome-free survivals were 95%, 85%, and 77%. The GLOBE and UK-PBC scores predicted cirrhosis-related complications better than the UDCA response criteria. The hazard ratio (HR) for a 1 standard deviation increase was HR 5.05 (95% confidence interval (CI): 4.43-5.74, P < 0.001) for the GLOBE score and HR 3.39 (95% CI: 3.10-3.72, P < 0.001) for the UK-PBC score. Overall, the GLOBE and UK-PBC risk scores showed similar and excellent prognostic performance (C-statistic, 0.93; 95% CI: 0.91%-95% vs 0.94; 95% CI: 0.91%-0.96%). DISCUSSION: In our international, multicenter PBC cohort, the GLOBE and UK-PBC risk scoring systems were good predictors of future cirrhosis-related complications.en_US
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPlacebo-controlled trialen_US
dc.subjectBiochemical responseen_US
dc.subjectHistological progressionen_US
dc.subjectCirrhosisen_US
dc.subjectBezafibrateen_US
dc.subjectPredictionen_US
dc.subjectPrognosisen_US
dc.subjectSurvivalen_US
dc.subjectOutcomesen_US
dc.subjectGlobeen_US
dc.subjectGastroenterology & hepatologyen_US
dc.subject.meshAdulten_US
dc.subject.meshAge factorsen_US
dc.subject.meshCholagogues and cholereticsen_US
dc.subject.meshCohort studiestr_TR
dc.subject.meshDisease Progressionen_US
dc.subject.meshDose-response relationship, drugen_US
dc.subject.meshDrug administration scheduleen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshInternationalityen_US
dc.subject.meshKaplan-Meier estimateen_US
dc.subject.meshLiver Cirrhosis, Biliaryen_US
dc.subject.meshMaleen_US
dc.subject.meshMiddle ageden_US
dc.subject.meshPredictive value of testsen_US
dc.subject.meshPrognosisen_US
dc.subject.meshProportional hazards modelsen_US
dc.subject.meshRetrospective studiesen_US
dc.subject.meshRisk Assessmenten_US
dc.subject.meshSeverity of illness indexen_US
dc.subject.meshSex factorsen_US
dc.subject.meshSurvival analysisen_US
dc.subject.meshTreatment outcomeen_US
dc.subject.meshUrsodeoxycholic aciden_US
dc.titleValidation of risk scoring systems in ursodeoxycholic acid-treated patients with primary biliary Cholangitisen_US
dc.typeArticleen_US
dc.identifier.wos000476563000018tr_TR
dc.identifier.scopus2-s2.0-85069274453tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentBursa Uludağ Üniversitesi/Tıp Fakültesi/Dahili Tıp Bilimleri.tr_TR
dc.contributor.orcid0000-0001-8126-2413tr_TR
dc.identifier.startpage1101tr_TR
dc.identifier.endpage1108tr_TR
dc.identifier.volume114tr_TR
dc.identifier.issue7tr_TR
dc.relation.journalAmerican Journal of Gastroenterologyen_US
dc.contributor.buuauthorEren, Fatih-
dc.contributor.researcheridAAS-6286-2020tr_TR
dc.relation.collaborationYurt dışıtr_TR
dc.relation.collaborationSanayitr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed31241547tr_TR
dc.subject.wosGastroenterology & hepatologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ1en_US
dc.contributor.scopusid12545949900tr_TR
dc.subject.scopusCholangitis; Biliary Liver Cirrhosis; Obeticholic Aciden_US
dc.subject.emtreeUrsodeoxycholic aciden_US
dc.subject.emtreeCholagogueen_US
dc.subject.emtreeAdolescenten_US
dc.subject.emtreeAdverse outcomeen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeAscitesen_US
dc.subject.emtreeBleedingen_US
dc.subject.emtreeCanadaen_US
dc.subject.emtreeChilden_US
dc.subject.emtreeCohort analysisen_US
dc.subject.emtreeConfidence intervalen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeEuropeen_US
dc.subject.emtreeEvent free survivalen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFollow upen_US
dc.subject.emtreeFranceen_US
dc.subject.emtreeHazard ratioen_US
dc.subject.emtreeHepatic encephalopathyen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMulticenter studyen_US
dc.subject.emtreePrimary biliary cirrhosisen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreePrognosisen_US
dc.subject.emtreeScoring systemen_US
dc.subject.emtreeSpainen_US
dc.subject.emtreeSurvival rateen_US
dc.subject.emtreeUnited Statesen_US
dc.subject.emtreeValidation studyen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAgeen_US
dc.subject.emtreeBiliary cirrhosisen_US
dc.subject.emtreeClinical trialen_US
dc.subject.emtreeDisease exacerbationen_US
dc.subject.emtreeDose responseen_US
dc.subject.emtreeDrug administrationen_US
dc.subject.emtreeInternational cooperationen_US
dc.subject.emtreeKaplan Meier methoden_US
dc.subject.emtreeMiddle ageden_US
dc.subject.emtreeMortalityen_US
dc.subject.emtreePathologyen_US
dc.subject.emtreePredictive valueen_US
dc.subject.emtreeProportional hazards modelen_US
dc.subject.emtreeRetrospective studyen_US
dc.subject.emtreeRisk assessmenten_US
dc.subject.emtreeSeverity of illness indexen_US
dc.subject.emtreeSex factoren_US
dc.subject.emtreeSurvival analysisen_US
dc.subject.emtreeTreatment outcomeen_US
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