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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorKIM, V.-
dc.contributor.authorABREU, R. M.-
dc.contributor.authorNAKAGAWA, D. M.-
dc.contributor.authorBALDASSARE, R. M.-
dc.contributor.authorCARRILHO, F. J.-
dc.contributor.authorONO, S. K.-
dc.date.accessioned2016-03-14T14:25:08Z-
dc.date.available2016-03-14T14:25:08Z-
dc.date.issued2016-
dc.identifier.citationJOURNAL OF VIRAL HEPATITIS, v.23, n.3, p.154-169, 2016-
dc.identifier.issn1352-0504-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/13434-
dc.description.abstractConventional interferon alfa and nucleos(t)ide analogues, such as lamivudine, are frequently used for chronic hepatitis B (CHB) treatment, but are associated with adverse effects and viral resistance. Here we performed a systematic review and meta-analysis evaluating all studies of pegylated interferon alfa (PEG-IFN) treatment in hepatitis B e antigen (HBeAg)-positive and HBeAg-negative patients with CHB. We searched electronic databases - PubMed, EMBASE, Cochrane Library and LILACS - for randomized controlled trials evaluating PEG-IFN therapy between 1999 and September 2014. Virological response was the primary outcome. We identified 14 studies involving 2829 patients. Our analysis revealed that PEG-IFN+lamivudine combination therapy produced better virological and biochemical responses than PEG-IFN monotherapy in HBeAg-positive and HBeAg-negative patients at the end of treatment. PEG-IFN+adefovir dipivoxil achieved better seroconversion rate than PEG-IFN in HBeAg-positive patients at the end of treatment. The present findings demonstrated a beneficial response rate following PEG-IFN combination therapy with nucelos(t)ides among HBeAg-positive and HBeAg-negative patients with CHB. Further trials are needed to investigate simultaneous and sequential therapy strategies.-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [576631/2008-6]-
dc.description.sponsorshipAlves de Queiroz Family Fund for Research-
dc.language.isoeng-
dc.publisherWILEY-BLACKWELL-
dc.relation.ispartofJournal of Viral Hepatitis-
dc.rightsrestrictedAccess-
dc.subjectchronic hepatitis B-
dc.subjectmeta-analysis-
dc.subjectpegylated interferon alfa-
dc.subjectrandomized controlled trials-
dc.subject.otherlamivudine combination therapy-
dc.subject.otherrandomized controlled-trial-
dc.subject.otherhbeag-negative patients-
dc.subject.otherpeginterferon alpha-2a-
dc.subject.otheradefovir dipivoxil-
dc.subject.otheracute exacerbation-
dc.subject.otherdisease burden-
dc.subject.othermonotherapy-
dc.subject.otherefficacy-
dc.subject.otherhbsag-
dc.titlePegylated interferon alfa for chronic hepatitis B: systematic review and meta-analysis-
dc.typearticle-
dc.rights.holderCopyright WILEY-BLACKWELL-
dc.identifier.doi10.1111/jvh.12418-
dc.identifier.pmid25967226-
dc.subject.wosGastroenterology & Hepatology-
dc.subject.wosInfectious Diseases-
dc.subject.wosVirology-
dc.type.categoryreview-
dc.type.versionpublishedVersion-
hcfmusp.description.beginpage154-
hcfmusp.description.endpage169-
hcfmusp.description.issue3-
hcfmusp.description.volume23-
hcfmusp.origemWOS-
hcfmusp.origem.id2-s2.0-84957432364-
hcfmusp.origem.idWOS:000369161000001-
hcfmusp.publisher.cityHOBOKEN-
hcfmusp.publisher.countryUSA-
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dc.description.indexMEDLINE-
dc.identifier.eissn1365-2893-
hcfmusp.citation.scopus31-
hcfmusp.scopus.lastupdate2024-04-12-
Appears in Collections:

Artigos e Materiais de Revistas Científicas - FM/MGT
Departamento de Gastroenterologia - FM/MGT

Artigos e Materiais de Revistas Científicas - HC/ICHC
Instituto Central - HC/ICHC

Artigos e Materiais de Revistas Científicas - HC/InRad
Instituto de Radiologia - HC/InRad

Artigos e Materiais de Revistas Científicas - LIM/07
LIM/07 - Laboratório de Gastroenterologia Clínica e Experimental

Artigos e Materiais de Revistas Científicas - ODS/03
ODS/03 - Saúde e bem-estar


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