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http://hdl.handle.net/11452/29979
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DC Field | Value | Language |
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dc.date.accessioned | 2022-12-20T08:46:30Z | - |
dc.date.available | 2022-12-20T08:46:30Z | - |
dc.date.issued | 2019-07 | - |
dc.identifier.citation | Efe, 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.issn | 0002-9270 | - |
dc.identifier.issn | 1572-0241 | - |
dc.identifier.uri | https://doi.org/10.14309/ajg.0000000000000290 | - |
dc.identifier.uri | https://journals.lww.com/ajg/Fulltext/2019/07000/Validation_of_Risk_Scoring_Systems_in.20.aspx | - |
dc.identifier.uri | http://hdl.handle.net/11452/29979 | - |
dc.description | Çalışmada 36 yazar bulunmaktadır. Bu yazarlardan sadece Bursa Uludağ Üniversitesi mensuplarının girişleri yapılmıştır. | tr_TR |
dc.description.abstract | INTRODUCTION: 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.iso | en | en_US |
dc.publisher | Lippincott Williams & Wilkins | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Placebo-controlled trial | en_US |
dc.subject | Biochemical response | en_US |
dc.subject | Histological progression | en_US |
dc.subject | Cirrhosis | en_US |
dc.subject | Bezafibrate | en_US |
dc.subject | Prediction | en_US |
dc.subject | Prognosis | en_US |
dc.subject | Survival | en_US |
dc.subject | Outcomes | en_US |
dc.subject | Globe | en_US |
dc.subject | Gastroenterology & hepatology | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Age factors | en_US |
dc.subject.mesh | Cholagogues and choleretics | en_US |
dc.subject.mesh | Cohort studies | tr_TR |
dc.subject.mesh | Disease Progression | en_US |
dc.subject.mesh | Dose-response relationship, drug | en_US |
dc.subject.mesh | Drug administration schedule | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Internationality | en_US |
dc.subject.mesh | Kaplan-Meier estimate | en_US |
dc.subject.mesh | Liver Cirrhosis, Biliary | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle aged | en_US |
dc.subject.mesh | Predictive value of tests | en_US |
dc.subject.mesh | Prognosis | en_US |
dc.subject.mesh | Proportional hazards models | en_US |
dc.subject.mesh | Retrospective studies | en_US |
dc.subject.mesh | Risk Assessment | en_US |
dc.subject.mesh | Severity of illness index | en_US |
dc.subject.mesh | Sex factors | en_US |
dc.subject.mesh | Survival analysis | en_US |
dc.subject.mesh | Treatment outcome | en_US |
dc.subject.mesh | Ursodeoxycholic acid | en_US |
dc.title | Validation of risk scoring systems in ursodeoxycholic acid-treated patients with primary biliary Cholangitis | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000476563000018 | tr_TR |
dc.identifier.scopus | 2-s2.0-85069274453 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Bursa Uludağ Üniversitesi/Tıp Fakültesi/Dahili Tıp Bilimleri. | tr_TR |
dc.contributor.orcid | 0000-0001-8126-2413 | tr_TR |
dc.identifier.startpage | 1101 | tr_TR |
dc.identifier.endpage | 1108 | tr_TR |
dc.identifier.volume | 114 | tr_TR |
dc.identifier.issue | 7 | tr_TR |
dc.relation.journal | American Journal of Gastroenterology | en_US |
dc.contributor.buuauthor | Eren, Fatih | - |
dc.contributor.researcherid | AAS-6286-2020 | tr_TR |
dc.relation.collaboration | Yurt dışı | tr_TR |
dc.relation.collaboration | Sanayi | tr_TR |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.identifier.pubmed | 31241547 | tr_TR |
dc.subject.wos | Gastroenterology & hepatology | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q1 | en_US |
dc.contributor.scopusid | 12545949900 | tr_TR |
dc.subject.scopus | Cholangitis; Biliary Liver Cirrhosis; Obeticholic Acid | en_US |
dc.subject.emtree | Ursodeoxycholic acid | en_US |
dc.subject.emtree | Cholagogue | en_US |
dc.subject.emtree | Adolescent | en_US |
dc.subject.emtree | Adverse outcome | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Ascites | en_US |
dc.subject.emtree | Bleeding | en_US |
dc.subject.emtree | Canada | en_US |
dc.subject.emtree | Child | en_US |
dc.subject.emtree | Cohort analysis | en_US |
dc.subject.emtree | Confidence interval | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Europe | en_US |
dc.subject.emtree | Event free survival | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Follow up | en_US |
dc.subject.emtree | France | en_US |
dc.subject.emtree | Hazard ratio | en_US |
dc.subject.emtree | Hepatic encephalopathy | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Major clinical study | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Multicenter study | en_US |
dc.subject.emtree | Primary biliary cirrhosis | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Prognosis | en_US |
dc.subject.emtree | Scoring system | en_US |
dc.subject.emtree | Spain | en_US |
dc.subject.emtree | Survival rate | en_US |
dc.subject.emtree | United States | en_US |
dc.subject.emtree | Validation study | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Age | en_US |
dc.subject.emtree | Biliary cirrhosis | en_US |
dc.subject.emtree | Clinical trial | en_US |
dc.subject.emtree | Disease exacerbation | en_US |
dc.subject.emtree | Dose response | en_US |
dc.subject.emtree | Drug administration | en_US |
dc.subject.emtree | International cooperation | en_US |
dc.subject.emtree | Kaplan Meier method | en_US |
dc.subject.emtree | Middle aged | en_US |
dc.subject.emtree | Mortality | en_US |
dc.subject.emtree | Pathology | en_US |
dc.subject.emtree | Predictive value | en_US |
dc.subject.emtree | Proportional hazards model | en_US |
dc.subject.emtree | Retrospective study | en_US |
dc.subject.emtree | Risk assessment | en_US |
dc.subject.emtree | Severity of illness index | en_US |
dc.subject.emtree | Sex factor | en_US |
dc.subject.emtree | Survival analysis | en_US |
dc.subject.emtree | Treatment outcome | en_US |
Appears in Collections: | PubMed Scopus Web of Science |
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