Impact of compensated cirrhosis on survival in patients with acute-on-chronic liver failure.

Acute-on-chronic liver failure Chronic liver disease Cirrhosis Liver injury Mortality Prognosis

Journal

Hepatology international
ISSN: 1936-0541
Titre abrégé: Hepatol Int
Pays: United States
ID NLM: 101304009

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 24 08 2021
accepted: 24 10 2021
pubmed: 26 11 2021
medline: 17 2 2022
entrez: 25 11 2021
Statut: ppublish

Résumé

Acute-on-chronic liver failure (ACLF) is considered a main prognostic event in patients with chronic liver disease (CLD). We analyzed the 28-day and 90-day mortality in ACLF patients with or without underlying cirrhosis enrolled in the ACLF Research Consortium (AARC) database. A total of 1,621 patients were prospectively enrolled and 637 (39.3%) of these patients had cirrhosis. Baseline characteristics, complications and mortality were compared between patients with and without cirrhosis. Alcohol consumption was more common in cirrhosis than non-cirrhosis (66.4% vs. 44.2%, p < 0.0001), while non-alcoholic fatty liver disease/cryptogenic CLD (10.9% vs 5.8%, p < 0.0001) and chronic HBV reactivation (18.8% vs 11.8%, p < 0.0001) were more common in non-cirrhosis. Only 0.8% of patients underwent liver transplantation. Overall, 28-day and 90-day mortality rates were 39.3% and 49.9%, respectively. Patients with cirrhosis had a greater chance of survival compared to those without cirrhosis both at 28-day (HR = 0.48; 95% CI 0.36-0.63, p < 0.0001) and 90-day (HR = 0.56; 95% CI 0.43-0.72, p < 0.0001), respectively. In alcohol CLD, non-cirrhosis patients had a higher 28-day (49.9% vs. 23.6%, p < 0.001) and 90-day (58.4% vs. 35.2%, p < 0.001) mortality rate than cirrhosis patients. ACLF patients with cirrhosis had longer mean survival than non-cirrhosis patients (25.5 vs. 18.8 days at 28-day and 65.2 vs. 41.2 days at 90-day). Exaggerated systemic inflammation might be the reason why non-cirrhosis patients had a poorer prognosis than those with cirrhosis after ACLF had occurred. The 28-day and 90-day mortality rates of ACLF patients without cirrhosis were significantly higher than those with cirrhosis in alcoholic CLD. The presence of cirrhosis and its stage should be evaluated at baseline to guide for management. Thai Clinical Trials Registry, TCTR20191226002.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Acute-on-chronic liver failure (ACLF) is considered a main prognostic event in patients with chronic liver disease (CLD). We analyzed the 28-day and 90-day mortality in ACLF patients with or without underlying cirrhosis enrolled in the ACLF Research Consortium (AARC) database.
METHODS METHODS
A total of 1,621 patients were prospectively enrolled and 637 (39.3%) of these patients had cirrhosis. Baseline characteristics, complications and mortality were compared between patients with and without cirrhosis.
RESULTS RESULTS
Alcohol consumption was more common in cirrhosis than non-cirrhosis (66.4% vs. 44.2%, p < 0.0001), while non-alcoholic fatty liver disease/cryptogenic CLD (10.9% vs 5.8%, p < 0.0001) and chronic HBV reactivation (18.8% vs 11.8%, p < 0.0001) were more common in non-cirrhosis. Only 0.8% of patients underwent liver transplantation. Overall, 28-day and 90-day mortality rates were 39.3% and 49.9%, respectively. Patients with cirrhosis had a greater chance of survival compared to those without cirrhosis both at 28-day (HR = 0.48; 95% CI 0.36-0.63, p < 0.0001) and 90-day (HR = 0.56; 95% CI 0.43-0.72, p < 0.0001), respectively. In alcohol CLD, non-cirrhosis patients had a higher 28-day (49.9% vs. 23.6%, p < 0.001) and 90-day (58.4% vs. 35.2%, p < 0.001) mortality rate than cirrhosis patients. ACLF patients with cirrhosis had longer mean survival than non-cirrhosis patients (25.5 vs. 18.8 days at 28-day and 65.2 vs. 41.2 days at 90-day). Exaggerated systemic inflammation might be the reason why non-cirrhosis patients had a poorer prognosis than those with cirrhosis after ACLF had occurred.
CONCLUSIONS CONCLUSIONS
The 28-day and 90-day mortality rates of ACLF patients without cirrhosis were significantly higher than those with cirrhosis in alcoholic CLD. The presence of cirrhosis and its stage should be evaluated at baseline to guide for management. Thai Clinical Trials Registry, TCTR20191226002.

Identifiants

pubmed: 34822057
doi: 10.1007/s12072-021-10266-8
pii: 10.1007/s12072-021-10266-8
pmc: PMC8844167
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

171-182

Subventions

Organisme : Ratchadaphiseksomphot Endowment Fund of hepatic fibrosis and cirrhosis research unit
ID : GRU 6105530009-1.

Investigateurs

Shiv Kumar Sarin (SK)
Ashok Choudhury (A)
Manoj K Sharma (MK)
Rakhi Maiwall (R)
Mamun Al Mahtab (MA)
Salimur Rahman (S)
Sanjiv Saigal (S)
Neeraj Saraf (N)
A S Soin (AS)
Harshad Devarbhavi (H)
Dong Joon Kim (DJ)
R K Dhiman (RK)
Ajay Duseja (A)
Sunil Taneja (S)
C E Eapen (CE)
Ashish Goel (A)
Q Ning (Q)
Tao Chen (T)
Ke Ma (K)
Z Duan (Z)
Chen Yu (C)
Sombat Treeprasertsuk (S)
S S Hamid (SS)
Amna S Butt (AS)
Wasim Jafri (W)
Akash Shukla (A)
Vivek Saraswat (V)
Soek Siam Tan (SS)
Ajit Sood (A)
Vandana Midha (V)
Omesh Goyal (O)
Hasmik Ghazinyan (H)
Anil Arora (A)
Jinhua Hu (J)
Manoj Sahu (M)
P N Rao (PN)
Guan H Lee (GH)
Seng G Lim (SG)
Laurentius A Lesmana (LA)
Cosmas Rinaldi Lesmana (CR)
Samir Shah (S)
V G Mohan Prasad (VG)
Diana A Payawal (DA)
Zaigham Abbas (Z)
A Kadir Dokmeci (A)
Jose D Sollano (JD)
Gian Carpio (G)
Ananta Shresta (A)
G K Lau (GK)
Md Fazal Karim (M)
Gamal Shiha (G)
Rino Gani (R)
Kemal Fariz Fariz Kalista (KFF)
Man-Fung Yuen (MF)
Seema Alam (S)
Rajeev Khanna (R)
Vikrant Sood (V)
Bikrant Bihari Lal (BB)
Viniyendra Pamecha (V)
Ankur Jindal (A)
V Rajan (V)
Vinod Arora (V)
Osamu Yokosuka (O)
Madunil A Niriella (MA)
Hai Li (H)
Xiaolong Qi (X)
Atsushi Tanaka (A)
Satoshi Mochida (S)
Dominic Ray Chaudhuri (DR)
Ed Gane (E)
Khin Maung Win (KM)
Wei Ting Chen (WT)
Mohd Rela (M)
Dharmesh Kapoor (D)
Amit Rastogi (A)
Pratibha Kale (P)
Archana Rastogi (A)
Chhagan Bihari Sharma (CB)
Meenu Bajpai (M)
Virender Singh (V)
Madhumita Premkumar (M)
Sudhir Sudhir (S)
A Olithselvan (A)
Cyriac Abby Philips (CA)
Anshu Srivastava (A)
Surender K Yachha (SK)
Zeeshan Ahmad Wani (ZA)
B R Thapa (BR)
Anoop Saraya (A)
None Shalimar
Ashish Kumar (A)
Manav Wadhawan (M)
Subash Gupta (S)
Kaushal Madan (K)
Puja Sakhuja (P)
Vivek Vij (V)
Barjesh C Sharma (BC)
Hitendra Garg (H)
Vishal Garg (V)
Chetan Kalal (C)
Lovkesh Anand (L)
Tanmay Vyas (T)
Rajan P Mathur (RP)
Guresh Kumar (G)
Priyanka Jain (P)
Samba Siva Rao Pasupuleti (SSR)
Yogesh K Chawla (YK)
Abhijit Chowdhury (A)
Shahinul Alam (S)
Do Seon Song (DS)
Jin Mo Yang (JM)

Informations de copyright

© 2021. The Author(s).

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Auteurs

Kessarin Thanapirom (K)

Division of Gastroenterology, Department of Medicine, Faculty of Medicine, Thai Red Cross, King Chulalongkorn Memorial Hospital, Chulalongkorn University, Pathumwan, Bangkok, Thailand.
Liver Fibrosis and Cirrhosis Research Unit, Chulalongkorn University, Bangkok, Thailand.

Tongluk Teerasarntipan (T)

Division of Gastroenterology, Department of Medicine, Faculty of Medicine, Thai Red Cross, King Chulalongkorn Memorial Hospital, Chulalongkorn University, Pathumwan, Bangkok, Thailand.

Sombat Treeprasertsuk (S)

Division of Gastroenterology, Department of Medicine, Faculty of Medicine, Thai Red Cross, King Chulalongkorn Memorial Hospital, Chulalongkorn University, Pathumwan, Bangkok, Thailand. battan5410@gmail.com.

Ashok Choudhury (A)

Department of Hepatology, Institute of Liver and Biliary Sciences, New Delhi, India.

Manoj K Sahu (MK)

IMS &SUM Hospital, Bhubaneswar, Odisha, India.

Rakhi Maiwall (R)

Department of Hepatology, Institute of Liver and Biliary Sciences, D-1, Vasant Kunj, New Delhi, India.

Viniyendra Pamecha (V)

Department of Liver Transplantation and Hepato Pancreatico Biliary Surgery, Institute of Liver and Biliary Sciences, New Delhi, India.

Richard Moreau (R)

EF Clif, EASL-CLIF Consortium and Grifols Chair, Barcelona, Spain.
Inserm, U1149, Centre de Recherche Sur L'Inflammation (CRI),, Paris, France.
UMRS1149, Université de Paris, Paris, France.
Service d'Hépatologie, Hôpital Beaujon, Assistance Publique-Hôpitaux de Paris, Clichy, France.

Mamun Al Mahtab (M)

Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.

Yogesh Kumar Chawla (YK)

PGIMER, Chandigarh, India.

Harshad Devarbhavi (H)

St John's Medical College, Bangalore, India.

Chen Yu (C)

Beijing Youan Hospital and Translational Hepatology Institute, Beijing, China.

Qin Ning (Q)

Tongji Hospital, Tongji Medical College, Wuhan, China.

Deepak Amarapurkar (D)

Department of Gastroenterology, Bombay Hospital and Medical Research Centre, Mumbai, India.

Chundamannil E Eapen (CE)

CMC, Vellore, India.

Saeed Sadiq Hamid (SS)

Aga Khan University Hospital, Karachi, Pakistan.

Amna Subhan Butt (AS)

Aga Khan University Hospital, Karachi, Pakistan.

Dong Joon Kim (DJ)

Hallym University College of Medicine, Chuncheon, South Korea.

Guan H Lee (GH)

Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.

Ajit Sood (A)

Dayanand Medical College, Ludhiana, India.

Laurentious A Lesmana (LA)

Digestive Disease & Oncology Centers, Medistra Hospital, Jakarta, Indonesia.

Zaigham Abbas (Z)

Ziauddin University, Karachi, Pakistan.

Gamal Shiha (G)

Egyptian Liver Research Institute and Hospital, Cairo, Egypt.

Diana A Payawal (DA)

Cardinal Santos Medical Center, San Jaun, Philippines.

Man-Fung Yuen (MF)

Queen Mary Hospital, The University of Hong Kong, Pok Fu Lam, Hong Kong.

Albert Chan (A)

Queen Mary Hospital, The University of Hong Kong, Pok Fu Lam, Hong Kong.

George Lau (G)

Department of Medicine, Humanity and Health Medical Group, New Kowloon, Hongkong, China.

Jidong Jia (J)

Friendship Hospital, Capital University, Beijing, China.

Salimur Rahman (S)

Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.

Barjesh C Sharma (BC)

Department of Hepatology, Institute of Liver and Biliary Sciences, D-1, Acharya Shree Tulsi Marg, Vasant Kunj, New Delhi, 110070, India.
Department of Advanced Endoscopy, Institute of Liver and Biliary Sciences, D-1, Acharya Shree Tulsi Marg, Vasant Kunj, New Delhi, 110070, India.

Osamu Yokosuka (O)

Chiba University, Chiba, Japan.

Shiv Kumar Sarin (SK)

Institute of Liver and Biliary Sciences, New Delhi, India.

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