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The PREDICT study uncovers three clinical courses of acutely decompensated cirrhosis that have distinct pathophysiology.

dc.contributor.authorTrebicka, Jonel
dc.contributor.authorFernandez, Javier
dc.contributor.authorPapp, Maria
dc.contributor.authorCaraceni, Paolo
dc.contributor.authorLaleman, Wim
dc.contributor.authorGambino, Carmine
dc.contributor.authorGiovo, Ilaria
dc.contributor.authorUschner, Frank Erhard
dc.contributor.authorJimenez, Cesar
dc.contributor.authorMookerjee, Rajeshwar
dc.contributor.authorGustot, Thierry
dc.contributor.authorAlbillos, Agustin
dc.contributor.authorBañares, Rafael
dc.contributor.authorJanicko, Martin
dc.contributor.authorSteib, Christian
dc.contributor.authorReiberger, Thomas
dc.contributor.authorAcevedo, Juan
dc.contributor.authorGatti, Pietro
dc.contributor.authorBernal, William
dc.contributor.authorZeuzem, Stefan
dc.contributor.authorZipprich, Alexander
dc.contributor.authorPiano, Salvatore
dc.contributor.authorBerg, Thomas
dc.contributor.authorBruns, Tony
dc.contributor.authorBendtsen, Flemming
dc.contributor.authorCoenraad, Minneke
dc.contributor.authorMerli, Manuela
dc.contributor.authorStauber, Rudolf
dc.contributor.authorZoller, Heinz
dc.contributor.authorRamos, José Presa
dc.contributor.authorSolè, Cristina
dc.contributor.authorSoriano, Germán
dc.contributor.authorde Gottardi, Andrea
dc.contributor.authorGronbaek, Henning
dc.contributor.authorSaliba, Faouzi
dc.contributor.authorTrautwein, Christian
dc.contributor.authorÖzdogan, Osman Cavit
dc.contributor.authorFrancque, Sven
dc.contributor.authorRyder, Stephen
dc.contributor.authorNahon, Pierre
dc.contributor.authorRomero-Gomez, Manuel
dc.contributor.authorVan Vlierberghe, Hans
dc.contributor.authorFrancoz, Claire
dc.contributor.authorManns, Michael
dc.contributor.authorGarcia, Elisabet
dc.contributor.authorTufoni, Manuel
dc.contributor.authorAmoros, Alex
dc.contributor.authorPavesi, Marco
dc.contributor.authorSanchez, Cristina
dc.contributor.authorCurto, Anna
dc.contributor.authorPitarch, Carla
dc.contributor.authorPutignano, Antonella
dc.contributor.authorMoreno, Esau
dc.contributor.authorShawcross, Debbie
dc.contributor.authorAguilar, Ferran
dc.contributor.authorClària, Joan
dc.contributor.authorPonzo, Paola
dc.contributor.authorJansen, Christian
dc.contributor.authorVitalis, Zsuzsanna
dc.contributor.authorZaccherini, Giacomo
dc.contributor.authorBalogh, Boglarka
dc.contributor.authorVargas, Victor
dc.contributor.authorMontagnese, Sara
dc.contributor.authorAlessandria, Carlo
dc.contributor.authorBernardi, Mauro
dc.contributor.authorGinès, Pere
dc.contributor.authorJalan, Rajiv
dc.contributor.authorMoreau, Richard
dc.contributor.authorAngeli, Paolo
dc.contributor.authorArroyo, Vicente
dc.contributor.authorPREDICT STUDY group of the EASL-CLIF Consortium
dc.date.accessioned2023-02-09T09:36:57Z
dc.date.available2023-02-09T09:36:57Z
dc.date.issued2020-07-13
dc.description.abstractAcute decompensation (AD) of cirrhosis is defined as the acute development of ascites, gastrointestinal hemorrhage, hepatic encephalopathy, infection or any combination thereof, requiring hospitalization. The presence of organ failure(s) in patients with AD defines acute-on-chronic liver failure (ACLF). The PREDICT study is a European, prospective, observational study, designed to characterize the clinical course of AD and to identify predictors of ACLF. A total of 1,071 patients with AD were enrolled. We collected detailed pre-specified information on the 3-month period prior to enrollment, and clinical and laboratory data at enrollment. Patients were then closely followed up for 3 months. Outcomes (liver transplantation and death) at 1 year were also recorded. Three groups of patients were identified. Pre-ACLF patients (n = 218) developed ACLF and had 3-month and 1-year mortality rates of 53.7% and 67.4%, respectively. Unstable decompensated cirrhosis (UDC) patients (n = 233) required ≥1 readmission but did not develop ACLF and had mortality rates of 21.0% and 35.6%, respectively. Stable decompensated cirrhosis (SDC) patients (n = 620) were not readmitted, did not develop ACLF and had a 1-year mortality rate of only 9.5%. The 3 groups differed significantly regarding the grade and course of systemic inflammation (high-grade at enrollment with aggravation during follow-up in pre-ACLF; low-grade at enrollment with subsequent steady-course in UDC; and low-grade at enrollment with subsequent improvement in SDC) and the prevalence of surrogates of severe portal hypertension throughout the study (high in UDC vs. low in pre-ACLF and SDC). Acute decompensation without ACLF is a heterogeneous condition with 3 different clinical courses and 2 major pathophysiological mechanisms: systemic inflammation and portal hypertension. Predicting the development of ACLF remains a major future challenge. CLINICALTRIALS. NCT03056612. Herein, we describe, for the first time, 3 different clinical courses of acute decompensation (AD) of cirrhosis after hospital admission. The first clinical course includes patients who develop acute-on-chronic liver failure (ACLF) and have a high short-term risk of death - termed pre-ACLF. The second clinical course (unstable decompensated cirrhosis) includes patients requiring frequent hospitalizations unrelated to ACLF and is associated with a lower mortality risk than pre-ACLF. Finally, the third clinical course (stable decompensated cirrhosis), includes two-thirds of all patients admitted to hospital with AD - patients in this group rarely require hospital admission and have a much lower 1-year mortality risk.
dc.identifier.doi10.1016/j.jhep.2020.06.013
dc.identifier.essn1600-0641
dc.identifier.pmid32673741
dc.identifier.unpaywallURLhttp://www.journal-of-hepatology.eu/article/S0168827820303846/pdf
dc.identifier.urihttp://hdl.handle.net/10668/15944
dc.issue.number4
dc.journal.titleJournal of hepatology
dc.journal.titleabbreviationJ Hepatol
dc.language.isoen
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number842-854
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeObservational Study
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAcute complications
dc.subjectChronic liver disease
dc.subjectNon-elective admission
dc.subjectOutcome
dc.subjectRisk factors
dc.subject.meshAcute-On-Chronic Liver Failure
dc.subject.meshEurope
dc.subject.meshFemale
dc.subject.meshFollow-Up Studies
dc.subject.meshHumans
dc.subject.meshHypertension, Portal
dc.subject.meshLiver Cirrhosis
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshPrognosis
dc.subject.meshProspective Studies
dc.subject.meshSeverity of Illness Index
dc.subject.meshSurvival Rate
dc.titleThe PREDICT study uncovers three clinical courses of acutely decompensated cirrhosis that have distinct pathophysiology.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number73
dspace.entity.typePublication

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