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

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

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BORIS DOI
10.48350/149883
Date of Publication
May 2021
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
Trebicka, Jonel
Fernandez, Javier
Papp, Maria
Caraceni, Paolo
Laleman, Wim
Gambino, Carmine
Giovo, Ilaria
Uschner, Frank Erhard
Jansen, Christian
Jimenez, Cesar
Mookerjee, Rajeshwar
Gustot, Thierry
Albillos, Agustin
Bañares, Rafael
Jarcuska, Peter
Steib, Christian
Reiberger, Thomas
Acevedo, Juan
Gatti, Pietro
Shawcross, Debbie L
Zeuzem, Stefan
Zipprich, Alexander
Piano, Salvatore
Berg, Thomas
Bruns, Tony
Danielsen, Karen Vagner
Coenraad, Minneke
Merli, Manuela
Stauber, Rudolf
Zoller, Heinz
Ramos, José Presa
Solé, Cristina
Soriano, Germán
De Gottardi, Andrea
Universitätsklinik für Viszerale Chirurgie und Medizin, Hepatologie
Gronbaek, Henning
Saliba, Faouzi
Trautwein, Christian
Kani, Haluk Tarik
Francque, Sven
Ryder, Stephen
Nahon, Pierre
Romero-Gomez, Manuel
Van Vlierberghe, Hans
Francoz, Claire
Manns, Michael
Garcia-Lopez, Elisabet
Tufoni, Manuel
Amoros, Alex
Pavesi, Marco
Sanchez, Cristina
Praktiknjo, Michael
Curto, Anna
Pitarch, Carla
Putignano, Antonella
Moreno, Esau
Bernal, William
Aguilar, Ferran
Clària, Joan
Ponzo, Paola
Vitalis, Zsuzsanna
Zaccherini, Giacomo
Balogh, Boglarka
Gerbes, Alexander
Vargas, Victor
Alessandria, Carlo
Bernardi, Mauro
Ginès, Pere
Moreau, Richard
Angeli, Paolo
Jalan, Rajiv
Arroyo, Vicente
Subject(s)

600 - Technology::610...

Series
Journal of hepatology
ISSN or ISBN (if monograph)
0168-8278
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.jhep.2020.11.019
PubMed ID
33227350
Uncontrolled Keywords

acute complications c...

Description
INTRODUCTION

Acute decompensation (AD) of cirrhosis may present without acute-on-chronic liver failure (ACLF) (AD-No ACLF), or with ACLF phenotype (AD-ACLF) defined by organ failure(s). Precipitants may induce AD. This multicenter, prospective, observational PREDICT study (NCT03056612) analyzes and characterizes the precipitants leading to both of these AD phenotypes.

PATIENTS AND METHODS

The PREDICT study included 1273 non-electively hospitalized patients with AD (No-ACLF=1071; ACLF=202). Medical history, clinical and laboratory data were collected at enrolment and during 90-day follow up, with particular attention to the following characteristics of precipitants: induction of organ dysfunction or failure, systemic inflammation, chronology, intensity, and relationship to outcome.

RESULTS

Among various clinical events, four distinct events were precipitants consistently related to AD, including proven bacterial infections, severe alcoholic hepatitis, gastrointestinal (GI) 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. In both AD phenotypes, patients with proven bacterial infections or severe alcoholic hepatitis had a similar survival. 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 lower ACLF development rate and lower 90-day mortality.

CONCLUSIONS

This study identified precipitants that are significantly associated with a distinct clinical course and prognosis of patients with AD and specific preventive and therapeutic strategies targeting these events may improve outcome in decompensated cirrhosis.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/38895
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