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PREDICT研究揭示了急性失代偿性肝硬化的三种具有不同病理生理学特征的临床病程。

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

作者信息

Trebicka Jonel, Fernandez Javier, Papp Maria, Caraceni Paolo, Laleman Wim, Gambino Carmine, Giovo Ilaria, Uschner Frank Erhard, Jimenez Cesar, Mookerjee Rajeshwar, Gustot Thierry, Albillos Agustin, Bañares Rafael, Janicko Martin, Steib Christian, Reiberger Thomas, Acevedo Juan, Gatti Pietro, Bernal William, Zeuzem Stefan, Zipprich Alexander, Piano Salvatore, Berg Thomas, Bruns Tony, Bendtsen Flemming, Coenraad Minneke, Merli Manuela, Stauber Rudolf, Zoller Heinz, Ramos José Presa, Solè Cristina, Soriano Germán, de Gottardi Andrea, Gronbaek Henning, Saliba Faouzi, Trautwein Christian, Özdogan Osman Cavit, Francque Sven, Ryder Stephen, Nahon Pierre, Romero-Gomez Manuel, Van Vlierberghe Hans, Francoz Claire, Manns Michael, Garcia Elisabet, Tufoni Manuel, Amoros Alex, Pavesi Marco, Sanchez Cristina, Curto Anna, Pitarch Carla, Putignano Antonella, Moreno Esau, Shawcross Debbie, Aguilar Ferran, Clària Joan, Ponzo Paola, Jansen Christian, Vitalis Zsuzsanna, Zaccherini Giacomo, Balogh Boglarka, Vargas Victor, Montagnese Sara, Alessandria Carlo, Bernardi Mauro, Ginès Pere, Jalan Rajiv, Moreau Richard, Angeli Paolo, Arroyo Vicente

机构信息

European Foundation for Study of Chronic Liver Failure, EF-Clif, Barcelona, Spain; JW Goethe University Hospital, Frankfurt, Germany.

European Foundation for Study of Chronic Liver Failure, EF-Clif, Barcelona, Spain; Hospital Clinic, IDIBAPS and CIBEehd, Barcelona, Spain.

出版信息

J Hepatol. 2020 Oct;73(4):842-854. doi: 10.1016/j.jhep.2020.06.013. Epub 2020 Jul 13.

Abstract

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.

摘要

背景与目的

肝硬化急性失代偿(AD)定义为腹水、胃肠道出血、肝性脑病、感染或上述情况的任意组合急性发作,需要住院治疗。AD患者出现器官功能衰竭则定义为慢加急性肝衰竭(ACLF)。PREDICT研究是一项欧洲前瞻性观察性研究,旨在描述AD的临床病程并确定ACLF的预测因素。

方法

共纳入1071例AD患者。我们收集了入组前3个月的详细预设信息以及入组时的临床和实验室数据。然后对患者进行3个月的密切随访。还记录了1年时的结局(肝移植和死亡)。

结果

确定了三组患者。ACLF前期患者(n = 218)发展为ACLF,3个月和1年死亡率分别为53.7%和67.4%。不稳定失代偿性肝硬化(UDC)患者(n = 233)需要≥1次再次入院但未发展为ACLF,死亡率分别为21.0%和35.6%。稳定失代偿性肝硬化(SDC)患者(n = 620)未再次入院,未发展为ACLF,1年死亡率仅为9.5%。三组在全身炎症的程度和病程(ACLF前期患者入组时炎症程度高,随访期间加重;UDC患者入组时炎症程度低,随后病程稳定;SDC患者入组时炎症程度低,随后改善)以及整个研究期间严重门静脉高压替代指标的患病率方面存在显著差异(UDC患者高,ACLF前期和SDC患者低)。

结论

无ACLF的急性失代偿是一种异质性疾病,有3种不同的临床病程和2种主要病理生理机制:全身炎症和门静脉高压。预测ACLF的发生仍然是未来的一项重大挑战。临床试验注册号:NCT03056612。

简要概述

在此,我们首次描述了肝硬化住院后急性失代偿(AD)的3种不同临床病程。第一种临床病程包括发展为慢加急性肝衰竭(ACLF)且短期死亡风险高的患者——称为ACLF前期。第二种临床病程(不稳定失代偿性肝硬化)包括需要频繁住院且与ACLF无关的患者,其死亡风险低于ACLF前期。最后,第三种临床病程(稳定失代偿性肝硬化)包括所有因AD入院患者的三分之二——该组患者很少需要住院,1年死亡风险低得多。

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