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Treatment of lamivudine-resistant chronic hepatitis B infection: a multicenter retrospective study

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dc.contributor.authorLee, Sun Jae-
dc.contributor.authorYim, Hyung Joon-
dc.contributor.authorHwang, Seong Gyu-
dc.contributor.authorSeo, Yeon Seok-
dc.contributor.authorKim, Ji Hoon-
dc.contributor.authorYoon, Eileen L.-
dc.contributor.authorLee, Joong Min-
dc.contributor.authorKim, Bo Hyun-
dc.contributor.authorPark, Sang Jong-
dc.contributor.authorPark, Young Min-
dc.contributor.authorKim, Hong Soo-
dc.contributor.authorLee, Se Hwan-
dc.contributor.authorAhn, Sang Hoon-
dc.contributor.authorLee, Jeong Il-
dc.contributor.authorLee, Jin Woo-
dc.contributor.authorKim, In Hee-
dc.contributor.authorKim, Hyung Soo-
dc.contributor.authorHong, Sun Pyo-
dc.date.accessioned2021-09-06T04:55:16Z-
dc.date.available2021-09-06T04:55:16Z-
dc.date.created2021-06-14-
dc.date.issued2013-02-
dc.identifier.issn0036-5521-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/104137-
dc.description.abstractObjectives. To compare the efficacy of rescue therapies in lamivudine (LAM)-resistant chronic hepatitis B (CHB) infections including: (1) adefovir dipivoxil (ADV) monotherapy, (2) ADV plus LAM combination therapy and (3) entecavir (ETV) 1.0 mg monotherapy. Materials and methods. The authors designed a multicenter-retrospective study. Eight institutions participated in the study from Korea. Results. A total of 343 LAM-resistant CHB patients were enrolled. The proportion of patients with undetectable serum hepatitis B virus (HBV) DNA levels at month 24 after the initiation of rescue therapy was higher in the ADV plus LAM combination therapy group (39/64, 60.9%) than in the ADV monotherapy (50/126, 39.7%) and ETV 1.0 mg monotherapy (19/48, 39.6%) groups (p = 0.014). Mean serum HBV DNA levels at 24 months were 2.07 +/- 1.21 log(10) IU/ml in the ADV plus LAM combination therapy group, 2.74 +/- 1.74 log(10) IU/ml in the ADV monotherapy group and 3.08 +/- 1.97 log(10) IU/ml in the ETV 1.0 mg monotherapy group (p = 0.014). In multivariate analysis, a finding of undetectable serum HBV DNA level at 6 months and ADV plus LAM combination therapy (vs. ADV) was an independent factor for predicting undetectable serum HBV DNA at month 24 (odds ratio, 1.003; 95% confidence interval, 1.000-1.006; p = 0.026). Conclusions. ADV plus LAM combination therapy is more effective in reducing viral load than switching to ADV or ETV 1.0 mg in patients with LAM-resistant CHB.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherINFORMA HEALTHCARE-
dc.subjectRESCUE THERAPY-
dc.subjectENTECAVIR RESISTANCE-
dc.subjectADEFOVIR MONOTHERAPY-
dc.subjectCOMBINATION THERAPY-
dc.subjectVIRUS INFECTION-
dc.subjectPLUS ADEFOVIR-
dc.subjectRISK-
dc.subjectSUBSTITUTIONS-
dc.subjectDIPIVOXIL-
dc.subjectGENOTYPES-
dc.titleTreatment of lamivudine-resistant chronic hepatitis B infection: a multicenter retrospective study-
dc.typeArticle-
dc.contributor.affiliatedAuthorYim, Hyung Joon-
dc.contributor.affiliatedAuthorSeo, Yeon Seok-
dc.contributor.affiliatedAuthorKim, Ji Hoon-
dc.identifier.doi10.3109/00365521.2012.722671-
dc.identifier.scopusid2-s2.0-84872701813-
dc.identifier.wosid000313675600009-
dc.identifier.bibliographicCitationSCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, v.48, no.2, pp.196 - 204-
dc.relation.isPartOfSCANDINAVIAN JOURNAL OF GASTROENTEROLOGY-
dc.citation.titleSCANDINAVIAN JOURNAL OF GASTROENTEROLOGY-
dc.citation.volume48-
dc.citation.number2-
dc.citation.startPage196-
dc.citation.endPage204-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaGastroenterology & Hepatology-
dc.relation.journalWebOfScienceCategoryGastroenterology & Hepatology-
dc.subject.keywordPlusRESCUE THERAPY-
dc.subject.keywordPlusENTECAVIR RESISTANCE-
dc.subject.keywordPlusADEFOVIR MONOTHERAPY-
dc.subject.keywordPlusCOMBINATION THERAPY-
dc.subject.keywordPlusVIRUS INFECTION-
dc.subject.keywordPlusPLUS ADEFOVIR-
dc.subject.keywordPlusRISK-
dc.subject.keywordPlusSUBSTITUTIONS-
dc.subject.keywordPlusDIPIVOXIL-
dc.subject.keywordPlusGENOTYPES-
dc.subject.keywordAuthoradefovir-
dc.subject.keywordAuthorantiviral resistance-
dc.subject.keywordAuthorchronic hepatitis B-
dc.subject.keywordAuthorcombination drug therapy-
dc.subject.keywordAuthorentecavir-
dc.subject.keywordAuthorlamivudine-
dc.subject.keywordAuthormulticenter study-
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