Evidence map›Paper›PMID 41846518›Full record

ReviewClinical and molecular hepatology2026

Severe hepatitis B flare and liver failure: current assessment and management.

Seng Gee Lim, Maria Buti, Jordan J Feld, James Fung, Adam J Gehring, K Rajender Reddy

Abstract readReview
In one paragraph

Review in Clinical and molecular hepatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Seng Gee LimDivision of Gastroenterology and Hepatology, Department of Medicine, National University Health System, Singapore. mdclimsg@nus.edu.sg.
Maria ButiLiver Unit, Hospital General Universitari Valle Hebron, Barcelona, Spain.
Jordan J FeldToronto Center for Liver Disease, Toronto General Hospital, University of Toronto, Toronto, ON, Canada.
James FungDepartment of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR.
Adam J GehringToronto Center for Liver Disease, Toronto General Hospital, University of Toronto, Toronto, ON, Canada.
K Rajender ReddyDepartment of Medicine, University of Pennsylvania, Philadelphia (K.R.R.), PA, USA.

Funding

National Medical Research Council NMRC/CIRG/1351/2013National Medical Research Council NMRC/CIRG/1479/2017National Medical Research Council NMRC/CSASI/0016/2017National Medical Research Council NMRC/OFLCG-19May-0038National Medical Research Council NMRC/TCR/014-NUHS/2015
6 · The paper itself

Abstract

Hepatitis B flare is a common complication of chronic hepatitis B and is defined as an increase in HBV viral load associated with abnormal alanine aminotransferases (ALT), the consensus being an ALT level ≥5 times the upper limit of normal. The immunopathogenesis is related to induction of inflammatory cells and cytokines by the rise in HBV DNA. There are multiple causes of flares, and they carry the risk of progression to hepatic decompensation and acute-on-chronic liver failure (ACLF) with associated mortality, potentially requiring liver transplantation. Initial assessment should exclude other causes of liver dysfunction and determine severity and prognosis. General prognostic models of ACLF are useful but the COSSH-ACLF II score is specific to HBV. Early initiation of nucleos(t)ide analogues is crucial, even in severe HBV flares; it can reduce mortality by 73.6%. Once jaundice and coagulopathy occur, salvage by antivirals is challenging, and liver transplantation should be considered. However, many patients may not be suitable candidates for transplant or donor livers may not be available, as is common in Asia. Recently, there has been increasing evidence of the benefits of adjunctive therapies such as corticosteroids and plasma exchange, but there are associated risks and these approaches should be considered rescue therapies in severe HBV flares or ACLF. Liver transplant is the ultimate intervention when these other strategies fail. In summary, HBV flares are clinically serious events that can lead to hepatic decompensation, ACLF, and the need for a donor liver; however, strategies for rescue should be considered before liver transplantation.

Indexed as

Hepatitis B, ChronicLiver FailureAcute-On-Chronic Liver FailureAlanine TransaminaseAntiviral AgentsDNA, ViralHepatitis B virusHumansLiver TransplantationPrognosisViral LoadAlanine TransaminaseAntiviral AgentsDNA, ViralAcute-on-chronic liver failureAlanine transaminaseHepatitis B, chronicHepatitis B, chronic/therapyPlasma exchange

Identifiers

PMID41846518
PMCPMC13430368

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.