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Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/19148
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dc.contributor.authorFerrante, M.en
dc.contributor.authorVermeire, S.en
dc.contributor.authorKatsanos, K. H.en
dc.contributor.authorNoman, M.en
dc.contributor.authorVan Assche, G.en
dc.contributor.authorSchnitzler, F.en
dc.contributor.authorArijs, I.en
dc.contributor.authorDe Hertogh, G.en
dc.contributor.authorHoffman, I.en
dc.contributor.authorGeboes, J. K.en
dc.contributor.authorRutgeerts, P.en
dc.date.accessioned2015-11-24T18:57:16Z-
dc.date.available2015-11-24T18:57:16Z-
dc.identifier.issn1078-0998-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/19148-
dc.rightsDefault Licence-
dc.subjectAdolescenten
dc.subjectAdulten
dc.subjectAgeden
dc.subjectAged, 80 and overen
dc.subjectAnti-Inflammatory Agents/*therapeutic useen
dc.subjectAntibodies, Monoclonal/*therapeutic useen
dc.subjectAzure Stainsen
dc.subjectChilden
dc.subjectColitis, Ulcerative/*drug therapy/pathologyen
dc.subjectColonoscopyen
dc.subjectFemaleen
dc.subjectGastrointestinal Agents/*therapeutic useen
dc.subjectHumansen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.titlePredictors of early response to infliximab in patients with ulcerative colitisen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1002/ibd.20054-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/17206703-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1002/ibd.20054/asset/20054_ftp.pdf?v=1&t=h0tajn0r&s=9017c15cd0cce21a83c22a46b24d9d06aede5412-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2007-
heal.abstractBACKGROUND: Our objective is to report the outcome of infliximab (IFX) in ulcerative colitis (UC) patients from a single center and to identify predictors of early clinical response. METHODS: The first 100 UC patients (45 female; median age, 37.9 years) who received IFX at a single center were included. Eighty-four patients received 5 mg/kg IFX, and 37 patients received a 3-dose IFX induction at weeks 0, 2, and 6. The Mayo endoscopic subscore, assessed by sigmoidoscopy before inclusion, was 1, 2, and 3 in 5%, 52%, and 43% of patients, respectively. Sixty percent had pancolitis, 63% were on concomitant immunosuppressive therapy, 9% were active smokers, 64% had C-reactive protein > or =5 mg/dL, and 44% were pANCA+/ASCA-. Five patients received IFX because of severe acute colitis refractory to intravenous corticosteroids. RESULTS: Early complete and partial clinical responses were observed in 41% and 24% of patients. Patients with early clinical response were significantly younger than nonresponders (median age, 35.7 versus 41.6 years, P = 0.041). Patients who were pANCA+/ASCA- had a significantly lower early clinical response (55% versus 76%; odds ratio [OR] = 0.40 (0.16-0.99), P = 0.049). Concomitant immunosuppressive therapy and the use of an IFX induction scheme did not influence early clinical response. Only 1 of 5 patients who received IFX for acute steroid-refractory colitis required colectomy within 2 months. CONCLUSIONS: IFX is an efficient therapy in UC, as shown by 65% early clinical response. A pANCA+/ASCA- serotype and an older age at first IFX infusion are associated with a suboptimal early clinical response.en
heal.journalNameInflamm Bowel Disen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
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