Identifying the early predictors of non-response to steroids in patients with flare of autoimmune hepatitis causing acute-on-chronic liver failure.


Journal

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

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 12 09 2022
accepted: 06 01 2023
medline: 31 7 2023
pubmed: 16 2 2023
entrez: 15 2 2023
Statut: ppublish

Résumé

Early identification of non-response to steroids is critical in patients with autoimmune hepatitis (AIH) causing acute-on-chronic liver failure (ACLF). We assessed if this non-response can be accurately identified within first few days of treatment. Patients with AIH-ACLF without baseline infection/hepatic encephalopathy were identified from APASL ACLF research consortium (AARC) database. Diagnosis of AIH-ACLF was based mainly on histology. Those treated with steroids were assessed for non-response (defined as death or liver transplant at 90 days for present study). Laboratory parameters, AARC, and model for end-stage liver disease (MELD) scores were assessed at baseline and day 3 to identify early non-response. Utility of dynamic SURFASA score [- 6.80 + 1.92*(D0-INR) + 1.94*(∆%3-INR) + 1.64*(∆%3-bilirubin)] was also evaluated. The performance of early predictors was compared with changes in MELD score at 2 weeks. Fifty-five out of one hundred and sixty-five patients (age-38.2 ± 15.0 years, 67.2% females) with AIH-ACLF [median MELD 24 (IQR: 22-27); median AARC score 7 (6-9)] given oral prednisolone 40 (20-40) mg per day were analyzed. The 90 day transplant-free survival in this cohort was 45.7% with worse outcomes in those with incident infections (56% vs 28.0%, p = 0.03). The AUROC of pre-therapy AARC score [0.842 (95% CI 0.754-0.93)], MELD [0.837 (95% CI 0.733-0.94)] score and SURFASA score [0.795 (95% CI 0.678-0.911)] were as accurate as ∆MELD at 2 weeks [0.770 (95% CI 0.687-0.845), p = 0.526] and better than ∆MELD at 3 days [0.541 (95% CI 0.395, 0.687), p < 0.001] to predict non-response. Combination of AARC score > 6, MELD score > 24 with SURFASA score ≥ - 1.2, could identify non-responders at day 3 (concomitant- 75% vs either - 42%, p < 0.001). Baseline AARC score, MELD score, and the dynamic SURFASA score on day 3 can accurately identify early non-response to steroids in AIH-ACLF.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
Early identification of non-response to steroids is critical in patients with autoimmune hepatitis (AIH) causing acute-on-chronic liver failure (ACLF). We assessed if this non-response can be accurately identified within first few days of treatment.
METHODS METHODS
Patients with AIH-ACLF without baseline infection/hepatic encephalopathy were identified from APASL ACLF research consortium (AARC) database. Diagnosis of AIH-ACLF was based mainly on histology. Those treated with steroids were assessed for non-response (defined as death or liver transplant at 90 days for present study). Laboratory parameters, AARC, and model for end-stage liver disease (MELD) scores were assessed at baseline and day 3 to identify early non-response. Utility of dynamic SURFASA score [- 6.80 + 1.92*(D0-INR) + 1.94*(∆%3-INR) + 1.64*(∆%3-bilirubin)] was also evaluated. The performance of early predictors was compared with changes in MELD score at 2 weeks.
RESULTS RESULTS
Fifty-five out of one hundred and sixty-five patients (age-38.2 ± 15.0 years, 67.2% females) with AIH-ACLF [median MELD 24 (IQR: 22-27); median AARC score 7 (6-9)] given oral prednisolone 40 (20-40) mg per day were analyzed. The 90 day transplant-free survival in this cohort was 45.7% with worse outcomes in those with incident infections (56% vs 28.0%, p = 0.03). The AUROC of pre-therapy AARC score [0.842 (95% CI 0.754-0.93)], MELD [0.837 (95% CI 0.733-0.94)] score and SURFASA score [0.795 (95% CI 0.678-0.911)] were as accurate as ∆MELD at 2 weeks [0.770 (95% CI 0.687-0.845), p = 0.526] and better than ∆MELD at 3 days [0.541 (95% CI 0.395, 0.687), p < 0.001] to predict non-response. Combination of AARC score > 6, MELD score > 24 with SURFASA score ≥ - 1.2, could identify non-responders at day 3 (concomitant- 75% vs either - 42%, p < 0.001).
CONCLUSION CONCLUSIONS
Baseline AARC score, MELD score, and the dynamic SURFASA score on day 3 can accurately identify early non-response to steroids in AIH-ACLF.

Identifiants

pubmed: 36790652
doi: 10.1007/s12072-023-10482-4
pii: 10.1007/s12072-023-10482-4
doi:

Substances chimiques

Prednisolone 9PHQ9Y1OLM

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

989-999

Informations de copyright

© 2023. Asian Pacific Association for the Study of the Liver.

Références

Mack CL, Adams D, Assis DN, et al. Diagnosis and management of autoimmune hepatitis in adults and children: 2019 practice guidance and guidelines from the American association for the study of liver diseases. Hepatology. 2020. https://doi.org/10.1002/hep.31065
doi: 10.1002/hep.31065 pubmed: 32500593
Rahim MN, Liberal R, Miquel R, Heaton ND, Heneghan MA. Acute severe autoimmune hepatitis: corticosteroids or liver transplantation? Liver Transpl. 2019;25(6):946–959. https://doi.org/10.1002/lt.25451
doi: 10.1002/lt.25451 pubmed: 30900368
Rahim MN, Miquel R, Heneghan MA. Approach to the patient with acute severe autoimmune hepatitis. JHEPReport. 2020;2:6. https://doi.org/10.1016/j.jhepr.2020.100149
doi: 10.1016/j.jhepr.2020.100149
Sarin SK, Choudhury A, Sharma MK, et al. Acute-on-chronic liver failure: consensus recommendations of the Asian Pacific association for the study of the liver (APASL): an update. Hepatol Int. 2019;13(4):353–390. https://doi.org/10.1007/s12072-019-09946-3
doi: 10.1007/s12072-019-09946-3 pubmed: 31172417
Yeoman AD, Westbrook RH, Zen Y, et al. Prognosis of acute severe autoimmune hepatitis (AS-AIH): the role of corticosteroids in modifying outcome. J Hepatol. 2014;61(4):876–882. https://doi.org/10.1016/j.jhep.2014.05.021
doi: 10.1016/j.jhep.2014.05.021 pubmed: 24842305
Zachou K, Arvaniti P, Azariadis K, et al. Prompt initiation of high-dose i.v. corticosteroids seems to prevent progression to liver failure in patients with original acute severe autoimmune hepatitis. Hepatol Res. 2019;49(1):96–104. https://doi.org/10.1111/hepr.13252
doi: 10.1111/hepr.13252 pubmed: 30248210
Anand L, Choudhury A, Bihari C, et al. Flare of autoimmune hepatitis causing acute on chronic liver failure: diagnosis and response to corticosteroid therapy. Hepatology. 2019;70(2):587–596. https://doi.org/10.1002/hep.30205
doi: 10.1002/hep.30205 pubmed: 30113706
Fujiwara K, Yasui S, Yokosuka O. Autoimmune acute liver failure: an emerging etiology for intractable acute liver failure. Hepatol Int. 2013;7(2):335–346. https://doi.org/10.1007/s12072-012-9402-3
doi: 10.1007/s12072-012-9402-3 pubmed: 26201768
Ichai P, Duclos-Vallée JC, Guettier C, et al. Usefulness of corticosteroids for the treatment of severe and fulminant forms of autoimmune hepatitis. Liver Transpl. 2007;13(7):996–1003. https://doi.org/10.1002/lt.21036
doi: 10.1002/lt.21036 pubmed: 17370335
Joshita S, Yoshizawa K, Umemura T, et al. Clinical features of autoimmune hepatitis with acute presentation: a Japanese nationwide survey. J Gastroenterol. 2018;53(9):1079–1088. https://doi.org/10.1007/s00535-018-1444-4
doi: 10.1007/s00535-018-1444-4 pubmed: 29476251
Martin ED, Coilly A, Chazouillères O, et al. Early liver transplantation for corticosteroid non-responders with acute severe autoimmune hepatitis: the SURFASA score. J Hepatol. 2021;74(6):1325–1334. https://doi.org/10.1016/j.jhep.2020.12.033
doi: 10.1016/j.jhep.2020.12.033 pubmed: 33503489
Noguchi F, Chu P, sung, Yoshida A, et al. Early dynamics of meld scores predict corticosteroid responsiveness to severe acute-onset autoimmune hepatitis. Clin Gastroenterol Hepatol. 2021. https://doi.org/10.1016/j.cgh.2021.06.006
doi: 10.1016/j.cgh.2021.06.006 pubmed: 34102339
Shalimar N, Kedia S, Mahapatra SJ, et al. Severity and outcome of acute-on-chronic liver failure is dependent on the etiology of acute hepatic insults: analysis of 368 patients. J Clin Gastroenterol. 2017;51(8):734–741. https://doi.org/10.1097/MCG.0000000000000823
doi: 10.1097/MCG.0000000000000823 pubmed: 28296656
Sharma S, Agarwal S, Gopi S, et al. Determinants of outcomes in autoimmune hepatitis presenting as acute on chronic liver failure without extrahepatic organ dysfunction upon treatment with steroids. J Clin Exp Hepatol. 2021;11(2):171–180. https://doi.org/10.1016/j.jceh.2020.08.007
doi: 10.1016/j.jceh.2020.08.007 pubmed: 33746441
Granito A, Muratori P, Muratori L. Acute-on-chronic liver failure: a complex clinical entity in patients with autoimmune hepatitis. J Hepatol. 2021. https://doi.org/10.1016/j.jhep.2021.06.035
doi: 10.1016/j.jhep.2021.06.035 pubmed: 34793869
Stravitz RT, Lefkowitch JH, Fontana RJ, et al. Autoimmune acute liver failure: proposed clinical and histological criteria. Hepatology. 2011;53(2):517–526. https://doi.org/10.1002/hep.24080
doi: 10.1002/hep.24080 pubmed: 21274872
Choudhury A, Jindal A, Maiwall R, et al. 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. Hepatol Int. 2017;11(5):461–471. https://doi.org/10.1007/s12072-017-9816-z
doi: 10.1007/s12072-017-9816-z pubmed: 28856540

Auteurs

Sanchit Sharma (S)

Department of Gastroenterology and Human Nutrition, All India Institute of Medical Sciences, New Delhi, 110026, India.

Samagra Agarwal (S)

Department of Gastroenterology and Human Nutrition, All India Institute of Medical Sciences, New Delhi, 110026, India.

Anoop Saraya (A)

Department of Gastroenterology and Human Nutrition, All India Institute of Medical Sciences, New Delhi, 110026, India. ansaraya@yahoo.com.

Ashok Kumar Choudhury (AK)

Department of Hepatology, Institute of Liver and Biliary Sciences, New Delhi, 110070, India.

Sanjiv Saigal (S)

Department of Hepatology, Medanta, Medicity, Gurugram, Haryana, India.

A S Soin (AS)

Department of Hepatology, Medanta, Medicity, Gurugram, Haryana, India.

Akash Shukla (A)

Department of Gastroenterology, LTMMC, Mumbai, Maharashtra, India.

Manoj K Sahu (MK)

Department of Hepatology, IMS and SUM Hospital, Bhubneshwar, Odhisha, India.

Laurentius A Lesmana (LA)

Department of Medicine, Medistra Hospital, Jakarta, Indonesia.

Renaldi C Lesmana (RC)

Department of Medicine, Medistra Hospital, Jakarta, Indonesia.

Samir N Shah (SN)

Department of Hepatology, Global Hospital, Mumbai, India.

Jinhua Hu (J)

Department of Medicine, 302 Military Hospital, Bejing, China.

Soek Siam Tan (SS)

Department of Medicine, Hospital Selayang, Bata Cabs, Selangor, Malaysia.

Dinesh Jothimani (D)

Department of Liver Transplant and Surgery, Dr. Rela Institute and Medical Centre, Chennai, India.

Mohammed Rela (M)

Department of Liver Transplant and Surgery, Dr. Rela Institute and Medical Centre, Chennai, India.

Hasmik L Ghazinyan (HL)

Department of Hepatology, Nork Clinical Hospital of Infectious Disease, Yerevan, Armenia.

D N Amrapurkar (DN)

Bombay Hospital, Mumbai, Maharashtra, India.

C E Eapen (CE)

Department of Hepatology, Christan Medical College, Vellore, India.

Ashish Goel (A)

Department of Hepatology, Christan Medical College, Vellore, India.

Diana Alcantra Payawal (DA)

Department of Medicine, Cardinal Santos Medical Center, Metro Manila, Philippines.

Saeed Hamid (S)

Department of Medicine, Aga Khan University Hospital, Karachi, Pakistan.

Amna S Butt (AS)

Department of Medicine, Aga Khan University Hospital, Karachi, Pakistan.

Duan Zhongping (D)

Translational Hepatology Institute Capital Medical University, Beijing You' an Hospital, Beijing, China.

Virender Singh (V)

Department of Hepatology, PGIMER, Chandigarh, India.

Ajay Duseja (A)

Department of Hepatology, PGIMER, Chandigarh, India.

Ajit Sood (A)

Department of Gastroenterology, Dayanand Medical College, Ludhiana, India.

Vandana Midha (V)

Department of Gastroenterology, Dayanand Medical College, Ludhiana, India.

Mamun Al Mahtab (M)

Department of Hepatology, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.

Dong Joon Kim (DJ)

Department of Internal Medicine, Hallym University College of Medicine, Seoul, Korea.

Qin Ning (Q)

Department of Medicine, Tongji Hospital, Tongji Medical College, Wuhan, China.

Anand V Kulkarni (AV)

Asian Institute of Gastroenterology, Hyderabad, India.

P N Rao (PN)

Asian Institute of Gastroenterology, Hyderabad, India.

Guan Huei Lee (GH)

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

Sombat Treeprasertsuk (S)

Department of Medicine, Chulalongkorn University, Bangkok, Thailand.

Xin Shaojie (X)

Medical School of Chinese PLA, Beijing, China.

Md Fazal Karim (MF)

Department of Hepatology, Sir Salimullah Medical College, Dhaka, Bangladesh.

Jose D Sollano (JD)

Department of Medicine, University of Santo Tomas, Manila, Philippines.

Kemal Fariz Kalista (KF)

Division of Hepatobiliary, Cipto Mangunkusuamo Hospital, University of Indonesia, Jakarta, Indonesia.

Rino Alvani Gani (RA)

Division of Hepatobiliary, Cipto Mangunkusuamo Hospital, University of Indonesia, Jakarta, Indonesia.

V G Mohan Prasad (VGM)

Department of Gastroenterology, VGM Hospital, Coimbatore, India.

Shiv Kumar Sarin (SK)

Department of Hepatology, Institute of Liver and Biliary Sciences, New Delhi, 110070, India. shivsarin@gmail.com.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH