Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25105
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dc.contributor.authorDikici, Bünyamin-
dc.contributor.authorÖzgenç, Funda-
dc.contributor.authorKalaycı, Ayhan Gazi-
dc.contributor.authorTargan, Şeref-
dc.contributor.authorSeli̇moğlu, Ayşe-
dc.contributor.authorDoğancı, Tümay-
dc.contributor.authorKansu, Aydan-
dc.contributor.authorTosun, Selma Yegane-
dc.contributor.authorArslan, Nur Ç.-
dc.contributor.authorKasırga, Erhun-
dc.contributor.authorBoşnak, Mehmet-
dc.date.accessioned2022-03-17T06:08:33Z-
dc.date.available2022-03-17T06:08:33Z-
dc.date.issued2004-02-
dc.identifier.citationÖzkan, T. B. vd. (2004). “Current therapeutic approaches in childhood chronic hepatitis B infection: A multicenter study”. Journal of Gastroenterology and Hepatology, 19(2), 127-133.en_US
dc.identifier.issn0815-9319-
dc.identifier.urihttps://doi.org/10.1111/j.1440-1746.2004.03209.x-
dc.identifier.urihttp://hdl.handle.net/11452/25105-
dc.description.abstractBackground and Aim: The aim of the present study was to compare the therapeutic efficacy of three different regimens in childhood chronic hepatitis B (CHB) infection. Methods: A total of 182 children with CHB infection were prospectively allocated to three random groups. Sixty-two patients in the first group received high-dose interferon (IFN)-alpha 2b (10 MU/m(2)) thrice/weekly alone for 6 months. In the second (n = 60) and third groups (n = 60), IFN-alpha was used for 6 months (5 MU/m(2)) thrice/weekly in combination with lamivudine (LAM) (4 mg/kg, maximum 100 mg/day) for 12 months. Lamivudine was started simultaneously with IFN in the second group, while it was started 2 months prior to IFN injections in the third group. Results: The initial mean alanine aminotransferase (ALT) values for the first, second and third groups were 109 +/- 93 IU/L, 101 +/- 64 IU/L and 92 +/- 42 IU/L, respectively (P > 0.05). At the end of the therapy, ALT values decreased to 82 +/- 111 IU/L, 38 +/- 41 IU/L and 29 +/- 16 IU/L in groups 1, 2 and 3, respectively. The mean ALT value of the first group was significantly different to the second and third groups (P = 0.046 and P = 0.002, respectively) at the end of the therapy and these differences were found to be sustained after 18 months. However, results in the second and third groups were similar (P > 0.05). There were no significant differences in HBeAg clearance and anti-HBe seroconversion at the initial stage, 12 months and 18 months between the three groups (P > 0.05). Hepatitis B virus (HBV) DNA clearance in the first group was different from the second and third groups, while the second and third groups had similar HBV DNA clearance ratios at 12 and 18 months. No significant difference was found in the complete response (normalization of ALT, clearance of HBV DNA and seroconversion of anti HBe) ratios of all groups (at 12 months: 28.8, 45.5, 35.8% and at 18 months 33.3, 49 and 34% in groups 1, 2 and 3, respectively, P > 0.05). Conclusions: Although the ALT normalization and HBV DNA clearance ratios of IFN plus LAM combination groups were better than the high-dose IFN-alpha monotherapy group, no significant difference was found in the complete response ratios of all three groups.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGastroenterology and hepatologyen_US
dc.subjectChildrenen_US
dc.subjectChronic hepatitis Ben_US
dc.subjectInterferon-alphaen_US
dc.subjectLamivudineen_US
dc.subjectTherapyen_US
dc.subjectCombination treatmenten_US
dc.subjectVirusen_US
dc.subjectLamivudineen_US
dc.subjectManagementen_US
dc.titleCurrent therapeutic approaches in childhood chronic hepatitis B infection: A multicenter studyen_US
dc.typeArticleen_US
dc.identifier.wos000189072800002tr_TR
dc.identifier.scopus2-s2.0-10744221461tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi.tr_TR
dc.contributor.orcid0000-0001-5740-9729tr_TR
dc.identifier.startpage127tr_TR
dc.identifier.endpage133tr_TR
dc.identifier.volume19tr_TR
dc.identifier.issue2tr_TR
dc.relation.journalJournal of Gastroenterology and Hepatologyen_US
dc.contributor.buuauthorÖzkan, Tanju Başarır-
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed14731120tr_TR
dc.subject.wosGastroenterology and hepatologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid7004474005tr_TR
dc.subject.scopusMutation; Lamivudine; Adefoviren_US
dc.subject.emtreeAlanine aminotransferaseen_US
dc.subject.emtreeAlpha2b interferonen_US
dc.subject.emtreeHepatitis B(e) antibodyen_US
dc.subject.emtreeHepatitis B(e) antigenen_US
dc.subject.emtreeLamivudineen_US
dc.subject.emtreeVirus DNAen_US
dc.subject.emtreeAbdominal painen_US
dc.subject.emtreeAdolescenten_US
dc.subject.emtreeAlopeciaen_US
dc.subject.emtreeArthralgiaen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeChilden_US
dc.subject.emtreeChronic hepatitisen_US
dc.subject.emtreeClearanceen_US
dc.subject.emtreeClinical trialen_US
dc.subject.emtreeControlled clinical trialen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDrug efficacyen_US
dc.subject.emtreeDrug megadoseen_US
dc.subject.emtreeFatigueen_US
dc.subject.emtreeFemaleen_US
dc.subject.emtreeFlu like syndromeen_US
dc.subject.emtreeGastrointestinal symptomen_US
dc.subject.emtreeHepatitis Ben_US
dc.subject.emtreeHepatitis B virusen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeInjectionen_US
dc.subject.emtreeMajor clinical studyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMonotherapyen_US
dc.subject.emtreeMulticenter studyen_US
dc.subject.emtreeMyalgiaen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeProspective studyen_US
dc.subject.emtreeSeroconversionen_US
dc.subject.emtreeTreatment outcomeen_US
dc.subject.emtreeWeight reductionen_US
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