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PREDICT identifies precipitating events associated with the clinical course of acutely decompensated cirrhosis.

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.authorJansen, Christian
dc.contributor.authorJimenez, Cesar
dc.contributor.authorMookerjee, Rajeshwar
dc.contributor.authorGustot, Thierry
dc.contributor.authorAlbillos, Agustin
dc.contributor.authorBañares, Rafael
dc.contributor.authorJarcuska, Peter
dc.contributor.authorSteib, Christian
dc.contributor.authorReiberger, Thomas
dc.contributor.authorAcevedo, Juan
dc.contributor.authorGatti, Pietro
dc.contributor.authorShawcross, Debbie L
dc.contributor.authorZeuzem, Stefan
dc.contributor.authorZipprich, Alexander
dc.contributor.authorPiano, Salvatore
dc.contributor.authorBerg, Thomas
dc.contributor.authorBruns, Tony
dc.contributor.authorDanielsen, Karen Vagner
dc.contributor.authorCoenraad, Minneke
dc.contributor.authorMerli, Manuela
dc.contributor.authorStauber, Rudolf
dc.contributor.authorZoller, Heinz
dc.contributor.authorRamos, José Presa
dc.contributor.authorSolé, Cristina
dc.contributor.authorSoriano, Germán
dc.contributor.authorde Gottardi, Andrea
dc.contributor.authorGronbaek, Henning
dc.contributor.authorSaliba, Faouzi
dc.contributor.authorTrautwein, Christian
dc.contributor.authorKani, Haluk Tarik
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-Lopez, Elisabet
dc.contributor.authorTufoni, Manuel
dc.contributor.authorAmoros, Alex
dc.contributor.authorPavesi, Marco
dc.contributor.authorSanchez, Cristina
dc.contributor.authorPraktiknjo, Michael
dc.contributor.authorCurto, Anna
dc.contributor.authorPitarch, Carla
dc.contributor.authorPutignano, Antonella
dc.contributor.authorMoreno, Esau
dc.contributor.authorBernal, William
dc.contributor.authorAguilar, Ferran
dc.contributor.authorClària, Joan
dc.contributor.authorPonzo, Paola
dc.contributor.authorVitalis, Zsuzsanna
dc.contributor.authorZaccherini, Giacomo
dc.contributor.authorBalogh, Boglarka
dc.contributor.authorGerbes, Alexander
dc.contributor.authorVargas, Victor
dc.contributor.authorAlessandria, Carlo
dc.contributor.authorBernardi, Mauro
dc.contributor.authorGinès, Pere
dc.contributor.authorMoreau, Richard
dc.contributor.authorAngeli, Paolo
dc.contributor.authorJalan, Rajiv
dc.contributor.authorArroyo, Vicente
dc.contributor.authorPREDICT STUDY group of the EASL-CLIF CONSORTIUM
dc.date.accessioned2023-02-09T10:37:39Z
dc.date.available2023-02-09T10:37:39Z
dc.date.issued2020-11-20
dc.description.abstractAcute decompensation (AD) of cirrhosis may present without acute-on-chronic liver failure (ACLF) (AD-No ACLF), or with ACLF (AD-ACLF), defined by organ failure(s). Herein, we aimed to analyze and characterize the precipitants leading to both of these AD phenotypes. The multicenter, prospective, observational PREDICT study (NCT03056612) included 1,273 non-electively hospitalized patients with AD (No ACLF = 1,071; ACLF = 202). Medical history, clinical data and laboratory data were collected at enrolment and during 90-day follow-up, with particular attention given to the following characteristics of precipitants: induction of organ dysfunction or failure, systemic inflammation, chronology, intensity, and relationship to outcome. Among various clinical events, 4 distinct events were precipitants consistently related to AD: proven bacterial infections, severe alcoholic hepatitis, gastrointestinal bleeding with shock and toxic encephalopathy. Among patients with precipitants in the AD-No ACLF cohort and the AD-ACLF cohort (38% and 71%, respectively), almost all (96% and 97%, respectively) showed proven bacterial infection and severe alcoholic hepatitis, either alone or in combination with other events. Survival was similar in patients with proven bacterial infections or severe alcoholic hepatitis in both AD phenotypes. The number of precipitants was associated with significantly increased 90-day mortality and was paralleled by increasing levels of surrogates for systemic inflammation. Importantly, adequate first-line antibiotic treatment of proven bacterial infections was associated with a lower ACLF development rate and lower 90-day mortality. This study identified precipitants that are significantly associated with a distinct clinical course and prognosis in patients with AD. Specific preventive and therapeutic strategies targeting these events may improve outcomes in patients with decompensated cirrhosis. Acute decompensation (AD) of cirrhosis is characterized by a rapid deterioration in patient health. Herein, we aimed to analyze the precipitating events that cause AD in patients with cirrhosis. Proven bacterial infections and severe alcoholic hepatitis, either alone or in combination, accounted for almost all (96-97%) cases of AD and acute-on-chronic liver failure. Whilst the type of precipitant was not associated with mortality, the number of precipitant(s) was. This study identified precipitants that are significantly associated with a distinct clinical course and prognosis of patients with AD. Specific preventive and therapeutic strategies targeting these events may improve patient outcomes.
dc.identifier.doi10.1016/j.jhep.2020.11.019
dc.identifier.essn1600-0641
dc.identifier.pmid33227350
dc.identifier.unpaywallURLhttp://www.journal-of-hepatology.eu/article/S0168827820337727/pdf
dc.identifier.urihttp://hdl.handle.net/10668/16653
dc.issue.number5
dc.journal.titleJournal of hepatology
dc.journal.titleabbreviationJ Hepatol
dc.language.isoen
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number1097-1108
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.meshBacterial Infections
dc.subject.meshDisease Progression
dc.subject.meshEurope
dc.subject.meshFemale
dc.subject.meshHepatitis, Alcoholic
dc.subject.meshHumans
dc.subject.meshInflammation
dc.subject.meshLiver Cirrhosis
dc.subject.meshMale
dc.subject.meshMedical History Taking
dc.subject.meshMiddle Aged
dc.subject.meshNeeds Assessment
dc.subject.meshOrgan Dysfunction Scores
dc.subject.meshPrecipitating Factors
dc.subject.meshPreventive Health Services
dc.subject.meshPrognosis
dc.titlePREDICT identifies precipitating events associated with the clinical course of acutely decompensated cirrhosis.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number74
dspace.entity.typePublication

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