Non‑cirrhotic portal fbrosis/idiopathic portal hypertension: APASL recommendations for diagnosis and management

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dc.authorid0000-0002-8909-2102
dc.contributor.authorShukla, Akash
dc.contributor.authorRockey, Don C.
dc.contributor.authorKamath, Patrick S.
dc.contributor.authorKleiner, David E.
dc.contributor.authorSingh, Ankita
dc.contributor.authorVaidya, Arun
dc.contributor.authorKoshy, Abraham
dc.contributor.authorGoel, Ashish
dc.contributor.authorDökmeci, A. Kadir
dc.contributor.authorMeena, Babulal
dc.contributor.authorPhilips, Cyriac Abby
dc.contributor.authorSharma, Chhagan Bihari
dc.contributor.authorÖrmeci, Necati
dc.contributor.authorSarin, Shiv Kumar
dc.date.accessioned2024-11-18T08:33:34Z
dc.date.available2024-11-18T08:33:34Z
dc.date.issued2024
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, İç Hastalıkları Ana Bilim Dalı
dc.description.abstractSince the Asian Pacific Association for the Study of the Liver (APASL) published guidelines on non-cirrhotic portal fibrosis/idiopathic portal hypertension in 2007, there has been a surge in new information, especially with the introduction of the term porto-sinusoidal vascular disorder (PSVD). Non-cirrhotic intra-hepatic causes of portal hypertension include disorders with a clearly identifiable etiology, such as schistosomiasis, as well as disorders with an unclear etiology such as non-cirrhotic portal fibrosis (NCPF), also termed idiopathic portal hypertension (IPH). This entity is being increasingly recognized as being associated with systemic disease and drug therapy, especially cancer therapy. An international working group with extensive expertise in portal hypertension was assigned with formulating consensus guidelines to clarify the definition, diagnosis, histological features, natural history, and management of NCPF/IPH, especially in the context of PSVD. The guidelines were prepared based on evidence from existing published literature. Whenever there was paucity of evidence, expert opinion was included after detailed deliberation. The goal of this manuscript, therefore, is to enhance the current understanding and help create global consensus on the issues surrounding NCPF/IPH.
dc.identifier.citationShukla, A., Rockey, D. C., Kamath, P. S., Kleiner, D. E., Singh, A., Vaidya, A., Koshy, A., Goel, A., Dökmeci, A. K., Meena, B., Philips, C. A., Sharma, C. B., Payawal, D. A., Kim, D. J., Lo, G. H., Han, G., Qureshi, H., Wanless, I. R., Jia, J., Sollano, J. D., … Sarin, S. K. (2024). Non-cirrhotic portal fibrosis/idiopathic portal hypertension: APASL recommendations for diagnosis and management. Hepatology International. https://doi.org/10.1007/s12072-024-10739-6
dc.identifier.doi10.1007/s12072-024-10739-6
dc.identifier.issn1936-0533
dc.identifier.issn1936-0541
dc.identifier.pmidPMID: 39546143
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1007/s12072-024-10739-6
dc.identifier.urihttps://hdl.handle.net/20.500.13055/855
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.indekslendigikaynak.otherSCI-E - Science Citation Index Expanded
dc.institutionauthorid0000-0002-8909-2102
dc.language.isoen
dc.publisherSpringer Nature
dc.relation.ispartofHepatology International
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAPASL Consensus
dc.subjectINCPH
dc.subjectIdiopathic Non-Cirrhotic Portal Hypertension
dc.subjectIncomplete Septal Cirrhosis
dc.subjectNCPF
dc.subjectNCPH
dc.subjectNodular Regenerative Hyperplasia
dc.subjectNon-Cirrhotic Portal Hypertension
dc.subjectObliterative Portal Venopathy
dc.subjectPortal Hypertension
dc.subjectPorto-Sinusoidal Vascular Disease
dc.subjectVariceal Bleed
dc.titleNon‑cirrhotic portal fbrosis/idiopathic portal hypertension: APASL recommendations for diagnosis and management
dc.typeArticle
dspace.entity.typePublication

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