Publication:
Best practices for screening, testing, diagnosing, and treating patients with hepatitis D (delta) virus based on global expert review and recent guidelines

dc.contributor.coauthorCornberg, Markus
dc.contributor.coauthorZoulim, Fabien
dc.contributor.coauthorGish, Robert
dc.contributor.coauthorJacobson, Ira M.
dc.contributor.coauthorKushner, Tatyana
dc.contributor.coauthorLampertico, Pietro
dc.contributor.coauthorRizzetto, Mario
dc.contributor.coauthorYurdaydin, Cihan
dc.contributor.coauthorManns, Michael
dc.date.accessioned2025-12-31T08:19:18Z
dc.date.available2025-12-31
dc.date.issued2025
dc.description.abstractBackgroundHepatitis D virus (HDV) represents the most severe form of human viral hepatitis, associated with rapid progression to cirrhosis and increased liver-related mortality. Globally, an estimated 9-19 million individuals are anti-HDV positive. To ensure early detetion, current guidelines recommend screening all HBsAg-positive individuals or, at a minimum, those with defined risk factors.MethodsThis expert consensus paper updates the current landscape of HDV management. Recommendations were derived from a structured expert panel discussion, incorporating recent evidence and clinical guideline developments, with a focus on screening, diagnosis, and antiviral therapy.ResultsThe panel emphasized the importance of systematic HDV screening in HBsAg-positive individuals. Therapeutic strategies aim at sustained HDV-RNA suppression and, ideally, HBV surface antigens (HBsAg) loss. Bulevirtide was recommended as a long-term monotherapy. Pegylated interferon alpha (PEG-IFN alpha), if used, should be limited to 48 weeks and tailored based on viral response and tolerability. Combination therapy with bulevirtide and PEG-IFN alpha may be considered in selected cases.ConclusionThis consensus provides updated recommendations for the screening, diagnosis, and treatment of HDV infection, highlighting the role of bulevirtide and individualized therapeutic approaches. As the treatment landscape continues to evolve, combination regimens and novel agents currently under investigation may offer additional options in the near future.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessgold
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipGilead Sciences
dc.identifier.doi10.1177/13596535251349380
dc.identifier.eissn2040-2058
dc.identifier.embargoNo
dc.identifier.issn1359-6535
dc.identifier.issue4
dc.identifier.pubmed41024346
dc.identifier.quartileN/A
dc.identifier.scopus2-s2.0-105017371788
dc.identifier.urihttps://doi.org/10.1177/13596535251349380
dc.identifier.urihttps://hdl.handle.net/20.500.14288/31447
dc.identifier.volume30
dc.identifier.wos001584250600001
dc.keywordshepatitis D virus
dc.keywordshepatitis delta
dc.keywordsepidemiology
dc.keywordsantiviral therapy
dc.keywordsbulevirtide
dc.language.isoeng
dc.publisherSAGE PUBLICATIONS LTD
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofAntiviral Therapy
dc.relation.openaccessNo
dc.rightsCopyrighted
dc.subjectInfectious Diseases
dc.subjectPharmacology & Pharmacy
dc.subjectVirology
dc.titleBest practices for screening, testing, diagnosing, and treating patients with hepatitis D (delta) virus based on global expert review and recent guidelines
dc.typeReview
dspace.entity.typePublication

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