Review article: current management of primary sclerosing cholangitis.

The management of primary sclerosing cholangitis (PSC) is hindered by incomplete understanding of the pathogenesis of the disease and the lack of good prognostic models. Few large randomized controlled trials of drug therapy have been published. Best practice in the management of PSC is currently ba...

Volledige beschrijving

Bibliografische gegevens
Hoofdauteurs: Cullen, SN, Chapman, R
Formaat: Journal article
Taal:English
Gepubliceerd in: 2005
_version_ 1826288969812279296
author Cullen, SN
Chapman, R
author_facet Cullen, SN
Chapman, R
author_sort Cullen, SN
collection OXFORD
description The management of primary sclerosing cholangitis (PSC) is hindered by incomplete understanding of the pathogenesis of the disease and the lack of good prognostic models. Few large randomized controlled trials of drug therapy have been published. Best practice in the management of PSC is currently based therefore on careful interpretation of the available evidence, close observation of individual patients and clinical experience of the disease. Drug therapy is useful for alleviating symptoms. Ursodeoxycholic acid may slow progression of the disease and reduce the frequency of complications. Consensus is emerging on the issues of screening for the malignant complications of PSC and the indications for liver transplantation are becoming broader and encompassing the earliest stages of cholangiocarcinoma. In view of the rarity of the disease in the general population, large international collaborations to study PSC are necessary to provide clearer answers in areas of uncertainty, and these are now beginning to emerge.
first_indexed 2024-03-07T02:21:46Z
format Journal article
id oxford-uuid:a42c3ca3-7410-4e49-a72d-70f3b1e01ae4
institution University of Oxford
language English
last_indexed 2024-03-07T02:21:46Z
publishDate 2005
record_format dspace
spelling oxford-uuid:a42c3ca3-7410-4e49-a72d-70f3b1e01ae42022-03-27T02:32:02ZReview article: current management of primary sclerosing cholangitis.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:a42c3ca3-7410-4e49-a72d-70f3b1e01ae4EnglishSymplectic Elements at Oxford2005Cullen, SNChapman, RThe management of primary sclerosing cholangitis (PSC) is hindered by incomplete understanding of the pathogenesis of the disease and the lack of good prognostic models. Few large randomized controlled trials of drug therapy have been published. Best practice in the management of PSC is currently based therefore on careful interpretation of the available evidence, close observation of individual patients and clinical experience of the disease. Drug therapy is useful for alleviating symptoms. Ursodeoxycholic acid may slow progression of the disease and reduce the frequency of complications. Consensus is emerging on the issues of screening for the malignant complications of PSC and the indications for liver transplantation are becoming broader and encompassing the earliest stages of cholangiocarcinoma. In view of the rarity of the disease in the general population, large international collaborations to study PSC are necessary to provide clearer answers in areas of uncertainty, and these are now beginning to emerge.
spellingShingle Cullen, SN
Chapman, R
Review article: current management of primary sclerosing cholangitis.
title Review article: current management of primary sclerosing cholangitis.
title_full Review article: current management of primary sclerosing cholangitis.
title_fullStr Review article: current management of primary sclerosing cholangitis.
title_full_unstemmed Review article: current management of primary sclerosing cholangitis.
title_short Review article: current management of primary sclerosing cholangitis.
title_sort review article current management of primary sclerosing cholangitis
work_keys_str_mv AT cullensn reviewarticlecurrentmanagementofprimarysclerosingcholangitis
AT chapmanr reviewarticlecurrentmanagementofprimarysclerosingcholangitis