ArticleiLIVER2023
Prednisolone therapy accelerates recovery of severe drug-induced liver injury: A prospective, randomized controlled study.
Article in iLIVER, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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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.
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Who cites it
4 citing papers in PubMed.
- Re-exploration of the pharmacotherapeutic strategy for drug-induced liver injury: a narrative review.Frontiers in medicine · 2026Review
- Risk assessment of daikenchuto-induced hepatobiliary injury in colon cancer patients post-colectomy: a retrospective cohort study.BMC complementary medicine and therapies · 2025Article
- Model Prediction of Infection Risk After Glucocorticoid Treatment for Severe Drug-Induced Liver Injury: Globulin is a Core Predictive Factor.Drug design, development and therapy · 2025Article
- Risk factors related to significant hepatic inflammation in patients with acute drug-induced liver injury.iLIVER · 2024Article
Corrections and comments
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Authors and funding
13 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background and aims: Drug-induced liver injury (DILI) is one of the most serious adverse drug reactions and its incidence has been increasing rapidly. Accumulating evidence suggests that immune activation and systemic inflammatory responses are very important in the progression of DILI. Corticosteroids are often used in DILI, but their clinical usefulness remains controversial. We therefore conducted a prospective, randomized controlled study to investigate whether corticosteroid therapy can accelerate recovery and reduce mortality in severe DILI (SDILI). Methods: SDILI patients with total bilirubin ≥171 μmol/L who presented to the Fifth Medical Center of Chinese PLA General Hospital, Beijing from 2016 to 2019 were randomly allocated to prednisolone and control groups. The endpoints were resolution of SDILI, defined as a decrease in total bilirubin of at least 35 μmol/L to <171 μmol/L, and overall survival at 6 months. Patients in the prednisolone group received prednisolone 60 mg/day therapy for the first 7 days. Patients with a decrease in total bilirubin of more than 35 μmol/L on day 8 continued on tapering doses of prednisolone; otherwise, prednisolone was discontinued. Results: On day 8, 50.75% (34/67) and 26.47% (18/68) of the participants in the prednisolone and control groups, respectively, achieved the primary endpoint ( Conclusion: Prednisolone therapy may accelerate the recovery of SDILI.
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