Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/73143
Title: Acute-on-chronic liver failure: Epidemiology, prognosis, and outcome of a multicenter study in Thai population
Authors: Sakkarin Chirapongsathorn
Tongluk Teerasarntipan
Krit Tipchaichatta
Tanita Suttichaimongkol
Naichaya Chamroonkul
Chalermrat Bunchorntavakul
Sith Siramolpiwat
Siwaporn Chainuvati
Abhasnee Sobhonslidsuk
Apinya Leerapun
Teerha Piratvisuth
Wattana Sukeepaisarnjaroen
Tawesak Tanwandee
Sombat Treeprasertsuk
Authors: Sakkarin Chirapongsathorn
Tongluk Teerasarntipan
Krit Tipchaichatta
Tanita Suttichaimongkol
Naichaya Chamroonkul
Chalermrat Bunchorntavakul
Sith Siramolpiwat
Siwaporn Chainuvati
Abhasnee Sobhonslidsuk
Apinya Leerapun
Teerha Piratvisuth
Wattana Sukeepaisarnjaroen
Tawesak Tanwandee
Sombat Treeprasertsuk
Keywords: Medicine
Issue Date: 1-Mar-2022
Abstract: Background and Aim: Acute-on-chronic liver failure (ACLF) leads to multi-organ failure related to high mortality rates. This study aimed to gather epidemiological data and validate a scoring system to predict mortality in ACLF. Methods: This retrospective cohort study collected data from multicenter tertiary care hospitals in Thailand. A total of 638 hospitalized patients (acute decompensated liver disease [ADLD], 292 patients; ACLF, 346 patients) from January 2019 to June 2020 were enrolled in this study. We compared the mortality rate at days 30 and 90 between patients with ADLD and ACLF. Areas under the receiver operating characteristic (AUROC) curves of chronic liver failure–sequential organ failure assessment (CLIF-SOFA) and other existing scoring systems were compared among patients with ACLF. Results: The incidence of patients with ACLF was 54%. The main cause of chronic liver disease was alcohol (38%), with sepsis (50%) as the most common precipitating factor. ACLF with coagulopathy (AUROC 0.58, 95% confidence interval [CI]: 0.52–0.64), metabolic acidosis (AUROC 0.58, 95% CI: 0.52–0.64), and high aspartate aminotransferase (AST) (AUROC 0.59, 95% CI: 0.53–0.66) were associated with high 30-day mortality. The 30-day mortality rate of patients with acute decompensation and patients with ACLF was 46 and 58%, respectively. Respiratory system (P = 0.001) failure was the major end result in ACLF and constituted a significant factor to predict mortality. The AUROC of CLIF-SOFA score was superior to that of the other predicted score (AUROC 0.64, 95% CI: 0.585–0.704). Conclusion: Patients with ACLF with more organ failure and high CLIF-SOFA score were associated with high short-term mortality. Future studies should include an ACLF prospective registry to confirm these finding.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85126019147&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/73143
ISSN: 23979070
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.