Flare of Autoimmune Hepatitis Causing Acute on Chronic Liver Failure: Diagnosis and Response to Corticosteroid Therapy.


Journal

Hepatology (Baltimore, Md.)
ISSN: 1527-3350
Titre abrégé: Hepatology
Pays: United States
ID NLM: 8302946

Informations de publication

Date de publication:
08 2019
Historique:
received: 13 01 2018
accepted: 25 06 2018
pubmed: 17 8 2018
medline: 19 6 2020
entrez: 17 8 2018
Statut: ppublish

Résumé

Autoimmune hepatitis (AIH) is considered less common in the Asia Pacific region. Due to this, AIH flare as a cause of acute on chronic liver failure (ACLF) is often overlooked and treatment delayed. We aimed at the defining clinical and histopathological spectrum and role of steroid therapy in AIH-ACLF. Patients with AIH-ACLF, prospectively recruited and followed between 2012 and 2017, were analyzed from the Asian Pacific Association for the Study of the Liver ACLF Research Consortium (AARC) data base. Diagnosis of AIH was confirmed using International Autoimmune Hepatitis Group score or simplified AIH score with histopathological evidence. Of 2,825 ACLF patients, 82 (2.9%) fulfilled criteria of AIH (age 42.1 ± 18.1 years, 70% female). At baseline, mean bilirubin was 18.6 ± 8.2 mg/dL, Child-Turcotte-Pugh score was 11.7 ± 1.4, and Model for End-Stage Liver Disease (MELD) score was 27.6 ± 6.5. Mean immunoglobulin G was 21.61 ± 7.32 g/dL, and this was elevated ≥1.1 times in 97% of cases; 49% were seronegative. Liver histology was available in 90%, with median histological activity index of 10 (interquartile range, 7-12); 90% with moderate to severe interface activity; 56% showing significant parenchymal necrosis (bridging and confluent necrosis); and cirrhosis in 42%. Twenty-eight (34%) patients received steroid therapy and showed shorter intensive care unit (ICU) stay (median 1.5 versus 4 days, P < 0.001) and improved 90-day survival (75% versus 48.1%, P = 0.02) with comparable incidence of sepsis (P = 0.32) compared to those who did not. Patients of advanced age, more severe liver disease (MELD >27; 83.3% sensitivity, 78.9% specificity, area under the receiver operating characteristic curve 0.86), presence of hepatic encephalopathy, and fibrosis grade ≥F3 had an unfavorable response to corticosteroid therapy. Conclusion: AIH presenting as ACLF is not uncommon in Asian patients; a low threshold for liver biopsy is needed to confirm the diagnosis as nearly half the patients are seronegative; early stratification to steroid therapy or liver transplantation (MELD >27, hepatic encephalopathy in ≥F3) would reduce ICU stay and improve outcomes.

Identifiants

pubmed: 30113706
doi: 10.1002/hep.30205
doi:

Substances chimiques

Glucocorticoids 0
Prednisolone 9PHQ9Y1OLM

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

587-596

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

© 2018 by the American Association for the Study of Liver Diseases.

Auteurs

Lovkesh Anand (L)

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

Ashok Choudhury (A)

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

Chhagan Bihari (C)

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

Barjesh C Sharma (BC)

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

Manoj Kumar (M)

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

Rakhi Maiwall (R)

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

Soek Siam Tan (S)

Hepatology, Selayang Hospital, Kepong, Malaysia.

Samir R Shah (SR)

Hepatology, Global Hospital, Mumbai, India.

Saeed Hamid (S)

Medicine, Aga Khan University, Karachi, Pakistan.

Amna S Butt (AS)

Medicine, Aga Khan University, Karachi, Pakistan.

Wasim Jafri (W)

Medicine, Aga Khan University, Karachi, Pakistan.

Yogesh K Chawla (YK)

PGIMER, Chandigarh, India.

Sunil Taneja (S)

PGIMER, Chandigarh, India.

Ajay Duseja (A)

PGIMER, Chandigarh, India.

Radha K Dhiman (RK)

PGIMER, Chandigarh, India.

Mamun Al Mahtab (MA)

Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.

Hasmik Ghazinyan (H)

Nork Clinical Hospital, Yerevan, Armenia.

Zhongping Duan (Z)

Hepatology, Youan Hospital, Capital Medical University, Beijing, China.

Yu Chen (Y)

Kem Hospital, Mumbai, India.

Akash Shukla (A)

Kem Hospital, Mumbai, India.

Jinhua Hu (J)

302 Hospital, Beijing, China.

Zaigham Abbas (Z)

Ziauddin University, Karachi, Pakistan.

Sombat Treeprasertsuk (S)

Chulalongkorn University, Bangkok, Thailand.

Laurentius A Lesmana (LA)

Medistra Hospital, Jakarta, Indonesia.

Cosmas R Lesmana (CR)

Medistra Hospital, Jakarta, Indonesia.

Jose D Sollano (JD)

University of Santos Tomas, Manila, Philippines.

Gian Carpio (G)

University of Santos Tomas, Manila, Philippines.

Manoj K Sahu (MK)

IMS & SUM Hospital, Odissa, India.

Guresh Kumar (G)

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

Shiv K Sarin (SK)

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

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