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Prednisone is not beneficial for the treatment of severe drug-induced liver injury: An observational study (STROBE compliant)

There is limited information about the effects of corticosteroids on severe drug-induced liver injury (DILI). This study aimed to investigate the efficacy and safety of prednisone in severe DILI. Ninety patients with severe DILI were enrolled and studied retrospectively. They were divided into predn...

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Autores principales: Wan, Yue-Meng, Wu, Jie-Fang, Li, Yu-Hua, Wu, Hua-Mei, Wu, Xi-Nan, Xu, Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6616446/
https://www.ncbi.nlm.nih.gov/pubmed/31261497
http://dx.doi.org/10.1097/MD.0000000000015886
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author Wan, Yue-Meng
Wu, Jie-Fang
Li, Yu-Hua
Wu, Hua-Mei
Wu, Xi-Nan
Xu, Ying
author_facet Wan, Yue-Meng
Wu, Jie-Fang
Li, Yu-Hua
Wu, Hua-Mei
Wu, Xi-Nan
Xu, Ying
author_sort Wan, Yue-Meng
collection PubMed
description There is limited information about the effects of corticosteroids on severe drug-induced liver injury (DILI). This study aimed to investigate the efficacy and safety of prednisone in severe DILI. Ninety patients with severe DILI were enrolled and studied retrospectively. They were divided into prednisone (n = 66) and control groups (n = 24), undergoing the same treatment regimen except that patients in the prednisone group received a median daily dose of 40 mg prednisone. The primary endpoint was severity reduction (serum total bilirubin [TBIL] <86 μmol/L). During the study, the cumulative rates of severity reduction at 4-, 8-, and 12 days were comparable between the 2 groups (prednisone versus control: 7.6%, 33.3%, and 60.6% versus 12.5%, 37.5%, and 66.7%, P = .331), and were markedly lower in the high-dose group than in the low-dose group (0%, 28.6%, and 35.7% versus 9.6%, 34.6%, and 67.3%, P = .012) or in the control group (0%, 28.6%, and 35.7% versus 12.5%, 37.5%, and 66.7%, P = .023). The 30-day overall survival rate in the prednisone group was significantly higher than in the control group (100% versus 91.7%, P = .018). Serum bilirubin and transaminase values gradually decreased in both groups, which were not significantly different mostly. Cox-regression models revealed that baseline TBIL (hazard ratio: 0.235; 95% confidence interval: 0.084–0.665; P = .006) was the only predictor for severity reduction. No severe adverse event was noted in both groups. Prednisone therapy is safe but not beneficial, and even detrimental at a daily dose > 40 mg for the treatment of severe DILI.
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spelling pubmed-66164462019-07-22 Prednisone is not beneficial for the treatment of severe drug-induced liver injury: An observational study (STROBE compliant) Wan, Yue-Meng Wu, Jie-Fang Li, Yu-Hua Wu, Hua-Mei Wu, Xi-Nan Xu, Ying Medicine (Baltimore) Research Article There is limited information about the effects of corticosteroids on severe drug-induced liver injury (DILI). This study aimed to investigate the efficacy and safety of prednisone in severe DILI. Ninety patients with severe DILI were enrolled and studied retrospectively. They were divided into prednisone (n = 66) and control groups (n = 24), undergoing the same treatment regimen except that patients in the prednisone group received a median daily dose of 40 mg prednisone. The primary endpoint was severity reduction (serum total bilirubin [TBIL] <86 μmol/L). During the study, the cumulative rates of severity reduction at 4-, 8-, and 12 days were comparable between the 2 groups (prednisone versus control: 7.6%, 33.3%, and 60.6% versus 12.5%, 37.5%, and 66.7%, P = .331), and were markedly lower in the high-dose group than in the low-dose group (0%, 28.6%, and 35.7% versus 9.6%, 34.6%, and 67.3%, P = .012) or in the control group (0%, 28.6%, and 35.7% versus 12.5%, 37.5%, and 66.7%, P = .023). The 30-day overall survival rate in the prednisone group was significantly higher than in the control group (100% versus 91.7%, P = .018). Serum bilirubin and transaminase values gradually decreased in both groups, which were not significantly different mostly. Cox-regression models revealed that baseline TBIL (hazard ratio: 0.235; 95% confidence interval: 0.084–0.665; P = .006) was the only predictor for severity reduction. No severe adverse event was noted in both groups. Prednisone therapy is safe but not beneficial, and even detrimental at a daily dose > 40 mg for the treatment of severe DILI. Wolters Kluwer Health 2019-06-28 /pmc/articles/PMC6616446/ /pubmed/31261497 http://dx.doi.org/10.1097/MD.0000000000015886 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle Research Article
Wan, Yue-Meng
Wu, Jie-Fang
Li, Yu-Hua
Wu, Hua-Mei
Wu, Xi-Nan
Xu, Ying
Prednisone is not beneficial for the treatment of severe drug-induced liver injury: An observational study (STROBE compliant)
title Prednisone is not beneficial for the treatment of severe drug-induced liver injury: An observational study (STROBE compliant)
title_full Prednisone is not beneficial for the treatment of severe drug-induced liver injury: An observational study (STROBE compliant)
title_fullStr Prednisone is not beneficial for the treatment of severe drug-induced liver injury: An observational study (STROBE compliant)
title_full_unstemmed Prednisone is not beneficial for the treatment of severe drug-induced liver injury: An observational study (STROBE compliant)
title_short Prednisone is not beneficial for the treatment of severe drug-induced liver injury: An observational study (STROBE compliant)
title_sort prednisone is not beneficial for the treatment of severe drug-induced liver injury: an observational study (strobe compliant)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6616446/
https://www.ncbi.nlm.nih.gov/pubmed/31261497
http://dx.doi.org/10.1097/MD.0000000000015886
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