TY - JOUR
T1 - The PREDICT study uncovers three clinical courses of acutely decompensated cirrhosis that have distinct pathophysiology
AU - Trebicka, Jonel
AU - Fernandez, Javier
AU - Papp, Maria
AU - Caraceni, Paolo
AU - Laleman, Wim
AU - Gambino, Carmine
AU - Giovo, Ilaria
AU - Uschner, Frank Erhard
AU - Jimenez, Cesar
AU - Mookerjee, Rajeshwar
AU - Gustot, Thierry
AU - Albillos, Agustin
AU - Bañares, Rafael
AU - Janicko, Martin
AU - Steib, Christian
AU - Reiberger, Thomas
AU - Acevedo, Juan
AU - Gatti, Pietro
AU - Bernal, William
AU - Zeuzem, Stefan
AU - Zipprich, Alexander
AU - Piano, Salvatore
AU - Berg, Thomas
AU - Bruns, Tony
AU - Bendtsen, Flemming
AU - Coenraad, Minneke
AU - Merli, Manuela
AU - Stauber, Rudolf
AU - Zoller, Heinz
AU - Ramos, José Presa
AU - Solé, Cristina
AU - Soriano, Germán
AU - de Gottardi, Andrea
AU - Gronbaek, Henning
AU - Saliba, Faouzi
AU - Trautwein, Christian
AU - Özdogan, Osman Cavit
AU - Francque, Sven
AU - Ryder, Stephen
AU - Nahon, Pierre
AU - Romero-Gomez, Manuel
AU - Van Vlierberghe, Hans
AU - Francoz, Claire
AU - Manns, Michael
AU - Garcia, Elisabet
AU - Tufoni, Manuel
AU - Amoros, Alex
AU - Pavesi, Marco
AU - Sanchez, Cristina
AU - Curto, Anna
AU - PREDICT STUDY group of the EASL-CLIF CONSORTIUM
AU - Danielsen , Karen
A2 - Gluud, Lise Lotte
N1 - Copyright © 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
PY - 2020/10/1
Y1 - 2020/10/1
N2 - Background & Aims: Acute 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. Methods: 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. Results: 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). Conclusions: 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.gov number: NCT03056612. Lay summary: 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.
AB - Background & Aims: Acute 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. Methods: 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. Results: 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). Conclusions: 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.gov number: NCT03056612. Lay summary: 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.
KW - Acute complications
KW - Chronic liver disease
KW - Non-elective admission
KW - Outcome
KW - Risk factors
UR - http://www.scopus.com/inward/record.url?scp=85088972261&partnerID=8YFLogxK
U2 - 10.1016/j.jhep.2020.06.013
DO - 10.1016/j.jhep.2020.06.013
M3 - Journal article
C2 - 32673741
SN - 0168-8278
VL - 73
SP - 842
EP - 854
JO - Journal of Hepatology
JF - Journal of Hepatology
IS - 4
ER -