Acute liver failure: redefining the syndromes

Existing definitions of clinical syndromes in acute liver failure do not accurately reflect important differences in clinical features and prognosis. Based on a large series of patients with acute liver failure treated at King's College Hospital, London between 1972 and 1985, we propose a new t...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Lancet (British edition) 1993-07, Vol.342 (8866), p.273-275
Hauptverfasser: Williams, R., Schalm, S.W., O'Grady, J.G.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 275
container_issue 8866
container_start_page 273
container_title The Lancet (British edition)
container_volume 342
creator Williams, R.
Schalm, S.W.
O'Grady, J.G.
description Existing definitions of clinical syndromes in acute liver failure do not accurately reflect important differences in clinical features and prognosis. Based on a large series of patients with acute liver failure treated at King's College Hospital, London between 1972 and 1985, we propose a new terminology. Hyperacute liver failure is our suggested term for cases in which encephalopathy occurs within 7 days of the onset of jaundice; this group includes the sizeable cohort likely to survive with medical management despite the high incidence of cerebral oedema. We suggest the term acute liver failure for cases with an interval of between 8 and 28 days from jaundice to encephalopathy; they also have a high incidence of cerebral oedema, but have a much poorer prognosis without liver transplantation. The term subacute liver failure is suggested to describe cases with encephalopathy that occurs within 5 to 12 weeks of the onset of jaundice; these patients are characterised by a low incidence of cerebral oedema, but have a poor prognosis. Adoption of this terminology should help in the management of these patients, in addition to standardising the structure and interpretation of controlled trials of therapies.
doi_str_mv 10.1016/0140-6736(93)91818-7
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_75847796</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>0140673693918187</els_id><sourcerecordid>1696810</sourcerecordid><originalsourceid>FETCH-LOGICAL-c413t-7225e8862115fe548f8b2c4c0c67d6e1bd9660ed600ffb9919e27de611fa3e113</originalsourceid><addsrcrecordid>eNp9kEtLxDAUhYMoOj7-gUIREV1Uc5s0DxfCMPgCwY2Cu9BJbjTSaTVphfn3dpxhFi5c3cX5zuHyEXII9AIoiEsKnOZCMnGm2bkGBSqXG2QEXPK85PJ1k4zWyA7ZTemDUsoFLbfJthoWGGUjko9t32FWh2-Mma9C3Ue8yiI69KEJzVvWvWOW5o2L7QzTPtnyVZ3wYHX3yMvtzfPkPn98unuYjB9zy4F1uSyKEpUSBUDpseTKq2lhuaVWSCcQpk4LQdEJSr2fag0aC-lQAPiKIQDbI6fL3c_YfvWYOjMLyWJdVw22fTKyVFxKLQbw-A_40faxGX4zoDWFQmk5QHwJ2dimFNGbzxhmVZwboGah0iw8mYUno5n5VWkWtaPVdj-doVuXVu6G_GSVV8lWtY9VY0NaY1yVkrFywK6XGA7CvgNGk2zAxqILEW1nXBv-_-MHrYCNGg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>199012897</pqid></control><display><type>article</type><title>Acute liver failure: redefining the syndromes</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><source>EBSCOhost Business Source Complete</source><source>ProQuest Central UK/Ireland</source><creator>Williams, R. ; Schalm, S.W. ; O'Grady, J.G.</creator><creatorcontrib>Williams, R. ; Schalm, S.W. ; O'Grady, J.G.</creatorcontrib><description>Existing definitions of clinical syndromes in acute liver failure do not accurately reflect important differences in clinical features and prognosis. Based on a large series of patients with acute liver failure treated at King's College Hospital, London between 1972 and 1985, we propose a new terminology. Hyperacute liver failure is our suggested term for cases in which encephalopathy occurs within 7 days of the onset of jaundice; this group includes the sizeable cohort likely to survive with medical management despite the high incidence of cerebral oedema. We suggest the term acute liver failure for cases with an interval of between 8 and 28 days from jaundice to encephalopathy; they also have a high incidence of cerebral oedema, but have a much poorer prognosis without liver transplantation. The term subacute liver failure is suggested to describe cases with encephalopathy that occurs within 5 to 12 weeks of the onset of jaundice; these patients are characterised by a low incidence of cerebral oedema, but have a poor prognosis. Adoption of this terminology should help in the management of these patients, in addition to standardising the structure and interpretation of controlled trials of therapies.</description><identifier>ISSN: 0140-6736</identifier><identifier>EISSN: 1474-547X</identifier><identifier>DOI: 10.1016/0140-6736(93)91818-7</identifier><identifier>PMID: 8101303</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>London: Elsevier Ltd</publisher><subject>Biological and medical sciences ; Classification ; Disease ; Gastroenterology. Liver. Pancreas. Abdomen ; Hepatic Encephalopathy - classification ; Humans ; Liver ; Liver Failure, Acute - classification ; Liver transplantation ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Medical research ; Medical sciences ; Other diseases. Semiology ; Terminology as Topic</subject><ispartof>The Lancet (British edition), 1993-07, Vol.342 (8866), p.273-275</ispartof><rights>1993</rights><rights>1993 INIST-CNRS</rights><rights>Copyright Lancet Ltd. Jul 31, 1993</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c413t-7225e8862115fe548f8b2c4c0c67d6e1bd9660ed600ffb9919e27de611fa3e113</citedby><cites>FETCH-LOGICAL-c413t-7225e8862115fe548f8b2c4c0c67d6e1bd9660ed600ffb9919e27de611fa3e113</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/199012897?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000,64390,64392,64394,72474</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=4857335$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8101303$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Williams, R.</creatorcontrib><creatorcontrib>Schalm, S.W.</creatorcontrib><creatorcontrib>O'Grady, J.G.</creatorcontrib><title>Acute liver failure: redefining the syndromes</title><title>The Lancet (British edition)</title><addtitle>Lancet</addtitle><description>Existing definitions of clinical syndromes in acute liver failure do not accurately reflect important differences in clinical features and prognosis. Based on a large series of patients with acute liver failure treated at King's College Hospital, London between 1972 and 1985, we propose a new terminology. Hyperacute liver failure is our suggested term for cases in which encephalopathy occurs within 7 days of the onset of jaundice; this group includes the sizeable cohort likely to survive with medical management despite the high incidence of cerebral oedema. We suggest the term acute liver failure for cases with an interval of between 8 and 28 days from jaundice to encephalopathy; they also have a high incidence of cerebral oedema, but have a much poorer prognosis without liver transplantation. The term subacute liver failure is suggested to describe cases with encephalopathy that occurs within 5 to 12 weeks of the onset of jaundice; these patients are characterised by a low incidence of cerebral oedema, but have a poor prognosis. Adoption of this terminology should help in the management of these patients, in addition to standardising the structure and interpretation of controlled trials of therapies.</description><subject>Biological and medical sciences</subject><subject>Classification</subject><subject>Disease</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Hepatic Encephalopathy - classification</subject><subject>Humans</subject><subject>Liver</subject><subject>Liver Failure, Acute - classification</subject><subject>Liver transplantation</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Other diseases. Semiology</subject><subject>Terminology as Topic</subject><issn>0140-6736</issn><issn>1474-547X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kEtLxDAUhYMoOj7-gUIREV1Uc5s0DxfCMPgCwY2Cu9BJbjTSaTVphfn3dpxhFi5c3cX5zuHyEXII9AIoiEsKnOZCMnGm2bkGBSqXG2QEXPK85PJ1k4zWyA7ZTemDUsoFLbfJthoWGGUjko9t32FWh2-Mma9C3Ue8yiI69KEJzVvWvWOW5o2L7QzTPtnyVZ3wYHX3yMvtzfPkPn98unuYjB9zy4F1uSyKEpUSBUDpseTKq2lhuaVWSCcQpk4LQdEJSr2fag0aC-lQAPiKIQDbI6fL3c_YfvWYOjMLyWJdVw22fTKyVFxKLQbw-A_40faxGX4zoDWFQmk5QHwJ2dimFNGbzxhmVZwboGah0iw8mYUno5n5VWkWtaPVdj-doVuXVu6G_GSVV8lWtY9VY0NaY1yVkrFywK6XGA7CvgNGk2zAxqILEW1nXBv-_-MHrYCNGg</recordid><startdate>19930731</startdate><enddate>19930731</enddate><creator>Williams, R.</creator><creator>Schalm, S.W.</creator><creator>O'Grady, J.G.</creator><general>Elsevier Ltd</general><general>Lancet</general><general>Elsevier Limited</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>0TT</scope><scope>0TZ</scope><scope>0U~</scope><scope>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7RV</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88C</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8C2</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>ASE</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FPQ</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K6X</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>KB~</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>19930731</creationdate><title>Acute liver failure: redefining the syndromes</title><author>Williams, R. ; Schalm, S.W. ; O'Grady, J.G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-7225e8862115fe548f8b2c4c0c67d6e1bd9660ed600ffb9919e27de611fa3e113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Biological and medical sciences</topic><topic>Classification</topic><topic>Disease</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Hepatic Encephalopathy - classification</topic><topic>Humans</topic><topic>Liver</topic><topic>Liver Failure, Acute - classification</topic><topic>Liver transplantation</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Other diseases. Semiology</topic><topic>Terminology as Topic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Williams, R.</creatorcontrib><creatorcontrib>Schalm, S.W.</creatorcontrib><creatorcontrib>O'Grady, J.G.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>News PRO</collection><collection>Pharma and Biotech Premium PRO</collection><collection>Global News &amp; ABI/Inform Professional</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Lancet Titles</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>British Nursing Index</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>Homework Central</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>British Nursing Index</collection><collection>Consumer Health Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Newsstand Professional</collection><collection>Biological Sciences</collection><collection>ProQuest Consumer Health Database</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>ProQuest Healthcare Administration Database</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Psychology Database</collection><collection>ProQuest Research Library</collection><collection>ProQuest Science Journals</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>The Lancet (British edition)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Williams, R.</au><au>Schalm, S.W.</au><au>O'Grady, J.G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute liver failure: redefining the syndromes</atitle><jtitle>The Lancet (British edition)</jtitle><addtitle>Lancet</addtitle><date>1993-07-31</date><risdate>1993</risdate><volume>342</volume><issue>8866</issue><spage>273</spage><epage>275</epage><pages>273-275</pages><issn>0140-6736</issn><eissn>1474-547X</eissn><coden>LANCAO</coden><abstract>Existing definitions of clinical syndromes in acute liver failure do not accurately reflect important differences in clinical features and prognosis. Based on a large series of patients with acute liver failure treated at King's College Hospital, London between 1972 and 1985, we propose a new terminology. Hyperacute liver failure is our suggested term for cases in which encephalopathy occurs within 7 days of the onset of jaundice; this group includes the sizeable cohort likely to survive with medical management despite the high incidence of cerebral oedema. We suggest the term acute liver failure for cases with an interval of between 8 and 28 days from jaundice to encephalopathy; they also have a high incidence of cerebral oedema, but have a much poorer prognosis without liver transplantation. The term subacute liver failure is suggested to describe cases with encephalopathy that occurs within 5 to 12 weeks of the onset of jaundice; these patients are characterised by a low incidence of cerebral oedema, but have a poor prognosis. Adoption of this terminology should help in the management of these patients, in addition to standardising the structure and interpretation of controlled trials of therapies.</abstract><cop>London</cop><pub>Elsevier Ltd</pub><pmid>8101303</pmid><doi>10.1016/0140-6736(93)91818-7</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0140-6736
ispartof The Lancet (British edition), 1993-07, Vol.342 (8866), p.273-275
issn 0140-6736
1474-547X
language eng
recordid cdi_proquest_miscellaneous_75847796
source MEDLINE; Elsevier ScienceDirect Journals Complete; EBSCOhost Business Source Complete; ProQuest Central UK/Ireland
subjects Biological and medical sciences
Classification
Disease
Gastroenterology. Liver. Pancreas. Abdomen
Hepatic Encephalopathy - classification
Humans
Liver
Liver Failure, Acute - classification
Liver transplantation
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Medical research
Medical sciences
Other diseases. Semiology
Terminology as Topic
title Acute liver failure: redefining the syndromes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-13T21%3A05%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Acute%20liver%20failure:%20redefining%20the%20syndromes&rft.jtitle=The%20Lancet%20(British%20edition)&rft.au=Williams,%20R.&rft.date=1993-07-31&rft.volume=342&rft.issue=8866&rft.spage=273&rft.epage=275&rft.pages=273-275&rft.issn=0140-6736&rft.eissn=1474-547X&rft.coden=LANCAO&rft_id=info:doi/10.1016/0140-6736(93)91818-7&rft_dat=%3Cproquest_cross%3E1696810%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=199012897&rft_id=info:pmid/8101303&rft_els_id=0140673693918187&rfr_iscdi=true