z-logo
open-access-imgOpen Access
Patterns of acute decompensation in hospitalized patients with cirrhosis and course of acute‐on‐chronic liver failure
Author(s) -
Balcar Lorenz,
Semmler Georg,
Pomej Katharina,
Simbrunner Benedikt,
Bauer David,
Hartl Lukas,
Jachs Mathias,
Paternostro Rafael,
Bucsics Theresa,
Pinter Matthias,
Trauner Michael,
Mandorfer Mattias,
Reiberger Thomas,
Scheiner Bernhard
Publication year - 2021
Publication title -
ueg journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.667
H-Index - 35
eISSN - 2050-6414
pISSN - 2050-6406
DOI - 10.1002/ueg2.12089
Subject(s) - medicine , decompensation , cirrhosis , gastroenterology , cohort , pathophysiology , retrospective cohort study , creatinine , complication
Abstract Introduction Recently, based on data from the PREDICT study, the European Foundation for the Study of Chronic Liver Failure (EF‐CLIF) consortium proposed pathophysiological/prognostic groups in hospitalized patients with cirrhosis: stable decompensated cirrhosis (SDC), unstable decompensated cirrhosis (UDC), pre‐acute‐on‐chronic liver failure (pre‐ACLF), and ACLF. We evaluated the outcomes of these subgroups in a real‐life cohort of hospitalized patients with cirrhosis. Methods Patients with cirrhosis developing first AD between 09/2010 and 12/2017 at the Vienna General Hospital were evaluated for this retrospective analysis. Results Two hundred and ten patients with cirrhosis (aged 57.6 ± 11.8 years) including n  = 45 (21.4%) SDC, n  = 100 (47.6%) UDC, n  = 28 (13.3%) pre‐ACLF, and n  = 37 (17.6%) with ACLF were considered. The proposed AD subgroups discriminated between patients with favorable (1‐year mortality: SDC: 6.7% and UDC: 19.6%) and dismal prognosis (90‐day mortality: pre‐ACLF: 42.9%). Interestingly, systemic inflammation gradually increased (e.g., C‐reactive protein, SDC: 0.9 mg/dl, vs. UDC: 2.0 mg/dl vs. pre‐ACLF: 3.2 mg/dl, p  < 0.001) while renal function was progressively deteriorating (creatinine levels, SDC: 0.8 mg/dl vs. UDC: 0.9 mg/dl vs. pre‐ACLF: 1.2 mg/dl, p  < 0.001) across prognostic subgroups in patients with cirrhosis. Discussion The recently proposed pathophysiological/prognostic EF‐CLIF subgroups are also reproduceable in a real‐life cohort of cirrhotic patients. As ACLF is a common and important complication, patients at risk of pre‐ACLF at index AD should be evaluated and if disease proceeds, been treated early and aggressively to avoid excessive mortality.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here