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Liver failure determines the outcome in patients of acute-on-chronic liver failure (ACLF): comparison of APASL ACLF research consortium (AARC) and CLIF-SOFA models.
Choudhury, A; Jindal, A; Maiwall, R; Sharma, M K; Sharma, B C; Pamecha, V; Mahtab, M; Rahman, S; Chawla, Y K; Taneja, S; Tan, S S; Devarbhavi, H; Duan, Z; Yu, Chen; Ning, Q; Jia, Ji Dong; Amarapurkar, D; Eapen, C E; Goel, A; Hamid, S S; Butt, A S; Jafri, W; Kim, D J; Ghazinian, H; Lee, G H; Sood, Ajit; Lesmana, L A; Abbas, Z; Shiha, G; Payawal, D A; Dokmeci, A K; Sollano, J D; Carpio, G; Lau, G K; Karim, F; Rao, P N; Moreau, R; Jain, P; Bhatia, P; Kumar, G; Sarin, S K.
Afiliação
  • Choudhury A; Department of Hepatology and Transplant, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.
  • Jindal A; Department of Hepatology, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.
  • Maiwall R; Department of Hepatology and Transplant, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.
  • Sharma MK; Department of Hepatology, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.
  • Sharma BC; Department of Hepatology and Transplant, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.
  • Pamecha V; Department of Hepatology, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.
  • Mahtab M; Department of Hepatology and Transplant, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.
  • Rahman S; Department of Hepatology, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.
  • Chawla YK; Department of Hepatology and Transplant, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.
  • Taneja S; Department of Hepatology, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.
  • Tan SS; Department of Hepatology and Transplant, Institute of Liver and Biliary Sciences (ILBS), New Delhi, 110 070, India.
  • Devarbhavi H; Department of Hepatology, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.
  • Duan Z; Department of Hepatology, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.
  • Yu C; Department of Hepatology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
  • Ning Q; Department of Hepatology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
  • Jia JD; Department of Gastroenterology and Hepatology, Selayang Hospital, Kepong, Malaysia.
  • Amarapurkar D; Department of Gastroenterology and Hepatology, St John Medical College, Bangalore, India.
  • Eapen CE; Beijing Youan Hospital, Capital Medical University, Beijing, China.
  • Goel A; Beijing Youan Hospital, Capital Medical University, Beijing, China.
  • Hamid SS; Department of Infectious Disease, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
  • Butt AS; Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
  • Jafri W; Department of Gastroenterology and Hepatology, Bombay Hospital and Medical Research Centre, Mumbai, India.
  • Kim DJ; Department of Gastrointestinal Sciences, Christian Medical College, Vellore, India.
  • Ghazinian H; Department of Gastrointestinal Sciences, Christian Medical College, Vellore, India.
  • Lee GH; Department of Medicine, Aga Khan University Hospital, Karachi, Pakistan.
  • Sood A; Department of Medicine, Aga Khan University Hospital, Karachi, Pakistan.
  • Lesmana LA; Department of Medicine, Aga Khan University Hospital, Karachi, Pakistan.
  • Abbas Z; Hallym University Chuncheon Sacred Heart Hospital, Center for Liver and Digestive Diseases, Chuncheon, Gangwon-Do, Republic of Korea.
  • Shiha G; Department of Hepatology, Nork Clinical Hospital of Infectious Diseases, Yerevan, Armenia.
  • Payawal DA; Department of Gastroenterology and Hepatology, National University Health System, Singapore, Singapore.
  • Dokmeci AK; Department of Gastroenterology, Dayanand Medical College, Ludhiana, India.
  • Sollano JD; Division of Hepatology, University of Indonesia, Jakarta, Indonesia.
  • Carpio G; Department of Hepatogastroenterology, Sindh Institute of Urology and Transplantation, Karachi, Pakistan.
  • Lau GK; Department of Internal Medicine, Egyptian Liver Research Institute and Hospital, Cairo, Egypt.
  • Karim F; Department of Hepatology, Cardinal Santos Medical Center, Manila, Philippines.
  • Rao PN; Department of Gastroenterology, Ankara University School of Medicine, Ankara, Turkey.
  • Moreau R; Cardinal Santos Medical Center, Metro Manila, Philippines.
  • Jain P; Cardinal Santos Medical Center, Metro Manila, Philippines.
  • Bhatia P; The Institute of Translational Hepatology, Beijing, China.
  • Kumar G; Sir Salimur Rehman Medical College, Mitford Hospital, Dhaka, Bangladesh.
  • Sarin SK; Asian Institute of Gastroenterology, Hyderabad, India.
Hepatol Int ; 11(5): 461-471, 2017 Sep.
Article em En | MEDLINE | ID: mdl-28856540
ABSTRACT
BACKGROUND AND

AIMS:

Acute-on-chronic liver failure (ACLF) is a progressive disease associated with rapid clinical worsening and high mortality. Early prediction of mortality and intervention can improve patient outcomes. We aimed to develop a dynamic prognostic model and compare it with the existing models.

METHODS:

A total of 1402 ACLF patients, enrolled in the APASL-ACLF Research Consortium (AARC) with 90-day follow-up, were analyzed. An ACLF score was developed in a derivation cohort (n = 480) and was validated (n = 922).

RESULTS:

The overall survival of ACLF patients at 28 days was 51.7%, with a median of 26.3 days. Five baseline variables, total bilirubin, creatinine, serum lactate, INR and hepatic encephalopathy, were found to be independent predictors of mortality, with AUROC in derivation and validation cohorts being 0.80 and 0.78, respectively. AARC-ACLF score (range 5-15) was found to be superior to MELD and CLIF SOFA scores in predicting mortality with an AUROC of 0.80. The point scores were categorized into grades of liver failure (Gr I 5-7; II 8-10; and III 11-15 points) with 28-day cumulative mortalities of 12.7, 44.5 and 85.9%, respectively. The mortality risk could be dynamically calculated as, with each unit increase in AARC-ACLF score above 10, the risk increased by 20%. A score of ≥11 at baseline or persisting in the first week was often seen among nonsurvivors (p = 0.001).

CONCLUSIONS:

The AARC-ACLF score is easy to use, dynamic and reliable, and superior to the existing prediction models. It can reliably predict the need for interventions, such as liver transplant, within the first week.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Escores de Disfunção Orgânica / Insuficiência Hepática Crônica Agudizada Tipo de estudo: Diagnostic_studies / Evaluation_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Escores de Disfunção Orgânica / Insuficiência Hepática Crônica Agudizada Tipo de estudo: Diagnostic_studies / Evaluation_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article