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Current therapeutic approaches in childhood chronic hepatitis B infection: A multicenter study

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.contributor.buuauthorÖzkan, Tanju Başarır
dc.contributor.departmentTıp Fakültesi
dc.contributor.orcid0000-0001-5740-9729
dc.contributor.scopusid7004474005
dc.date.accessioned2022-03-17T06:08:33Z
dc.date.available2022-03-17T06:08:33Z
dc.date.issued2004-02
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.
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.
dc.identifier.doi10.1111/j.1440-1746.2004.03209.x
dc.identifier.endpage133
dc.identifier.issn0815-9319
dc.identifier.issue2
dc.identifier.pubmed14731120
dc.identifier.scopus2-s2.0-10744221461
dc.identifier.startpage127
dc.identifier.urihttps://doi.org/10.1111/j.1440-1746.2004.03209.x
dc.identifier.urihttp://hdl.handle.net/11452/25105
dc.identifier.volume19
dc.identifier.wos000189072800002
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherWiley
dc.relation.collaborationYurt içi
dc.relation.journalJournal of Gastroenterology and Hepatology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectGastroenterology and hepatology
dc.subjectChildren
dc.subjectChronic hepatitis B
dc.subjectInterferon-alpha
dc.subjectLamivudine
dc.subjectTherapy
dc.subjectCombination treatment
dc.subjectVirus
dc.subjectLamivudine
dc.subjectManagement
dc.subject.emtreeAlanine aminotransferase
dc.subject.emtreeAlpha2b interferon
dc.subject.emtreeHepatitis B(e) antibody
dc.subject.emtreeHepatitis B(e) antigen
dc.subject.emtreeLamivudine
dc.subject.emtreeVirus DNA
dc.subject.emtreeAbdominal pain
dc.subject.emtreeAdolescent
dc.subject.emtreeAlopecia
dc.subject.emtreeArthralgia
dc.subject.emtreeArticle
dc.subject.emtreeChild
dc.subject.emtreeChronic hepatitis
dc.subject.emtreeClearance
dc.subject.emtreeClinical trial
dc.subject.emtreeControlled clinical trial
dc.subject.emtreeControlled study
dc.subject.emtreeDrug efficacy
dc.subject.emtreeDrug megadose
dc.subject.emtreeFatigue
dc.subject.emtreeFemale
dc.subject.emtreeFlu like syndrome
dc.subject.emtreeGastrointestinal symptom
dc.subject.emtreeHepatitis B
dc.subject.emtreeHepatitis B virus
dc.subject.emtreeHuman
dc.subject.emtreeInjection
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMale
dc.subject.emtreeMonotherapy
dc.subject.emtreeMulticenter study
dc.subject.emtreeMyalgia
dc.subject.emtreePriority journal
dc.subject.emtreeProspective study
dc.subject.emtreeSeroconversion
dc.subject.emtreeTreatment outcome
dc.subject.emtreeWeight reduction
dc.subject.scopusMutation; Lamivudine; Adefovir
dc.subject.wosGastroenterology and hepatology
dc.titleCurrent therapeutic approaches in childhood chronic hepatitis B infection: A multicenter study
dc.typeArticle
dc.wos.quartileQ2
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi
local.indexed.atScopus
local.indexed.atWOS

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