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Bicyclol for the treatment of drug-induced liver injury: a propensity score matching analysis using a nationwide inpatient database

OBJECTIVE: To evaluate the efficacy and safety of bicyclol in patients with drug-induced liver injury (DILI) using a nationwide database. METHODS: We retrospectively analyzed the clinical data of DILI patients in the DILI-R database. Propensity score matching was performed to balance the bicyclol an...

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Autores principales: Wang, Yongfeng, Lai, Rongtao, Zong, Peilan, Xu, Qingling, Shang, Jia, Zhang, Xia, Zhong, Wei, Tang, Jieting, Han, Xi’an, Chen, Chengwei, Mao, Yimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8059044/
https://www.ncbi.nlm.nih.gov/pubmed/33853430
http://dx.doi.org/10.1177/03000605211005945
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author Wang, Yongfeng
Lai, Rongtao
Zong, Peilan
Xu, Qingling
Shang, Jia
Zhang, Xia
Zhong, Wei
Tang, Jieting
Han, Xi’an
Chen, Chengwei
Mao, Yimin
author_facet Wang, Yongfeng
Lai, Rongtao
Zong, Peilan
Xu, Qingling
Shang, Jia
Zhang, Xia
Zhong, Wei
Tang, Jieting
Han, Xi’an
Chen, Chengwei
Mao, Yimin
author_sort Wang, Yongfeng
collection PubMed
description OBJECTIVE: To evaluate the efficacy and safety of bicyclol in patients with drug-induced liver injury (DILI) using a nationwide database. METHODS: We retrospectively analyzed the clinical data of DILI patients in the DILI-R database. Propensity score matching was performed to balance the bicyclol and control groups, and alanine aminotransferase (ALT) recovery was compared between the two groups. Factors associated with ALT recovery and safety were identified. RESULTS: The analysis included the data of 25,927 patients. Eighty-seven cases were included in the bicyclol group, with 932 cases in the control group. One-to-one propensity score matching created 86 matched pairs. The ALT normalization rate in the bicyclol group was significantly higher than that in the control group (50.00% vs. 24.42%), and statistical significance was found in the superiority test. After adjustment of baseline ALT levels, baseline total bilirubin levels, sex, age, acute or chronic liver diseases, and suspected drugs in the multivariate logic regression analysis, the major influencing factors for ALT recovery included the time interval between ALT tests (days) and the group factor (bicyclol treatment). There were no differences in the proportion of renal function impairment or blood abnormalities between the two groups. CONCLUSIONS: Bicyclol is a potential candidate for DILI.
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spelling pubmed-80590442021-05-04 Bicyclol for the treatment of drug-induced liver injury: a propensity score matching analysis using a nationwide inpatient database Wang, Yongfeng Lai, Rongtao Zong, Peilan Xu, Qingling Shang, Jia Zhang, Xia Zhong, Wei Tang, Jieting Han, Xi’an Chen, Chengwei Mao, Yimin J Int Med Res Retrospective Clinical Research Report OBJECTIVE: To evaluate the efficacy and safety of bicyclol in patients with drug-induced liver injury (DILI) using a nationwide database. METHODS: We retrospectively analyzed the clinical data of DILI patients in the DILI-R database. Propensity score matching was performed to balance the bicyclol and control groups, and alanine aminotransferase (ALT) recovery was compared between the two groups. Factors associated with ALT recovery and safety were identified. RESULTS: The analysis included the data of 25,927 patients. Eighty-seven cases were included in the bicyclol group, with 932 cases in the control group. One-to-one propensity score matching created 86 matched pairs. The ALT normalization rate in the bicyclol group was significantly higher than that in the control group (50.00% vs. 24.42%), and statistical significance was found in the superiority test. After adjustment of baseline ALT levels, baseline total bilirubin levels, sex, age, acute or chronic liver diseases, and suspected drugs in the multivariate logic regression analysis, the major influencing factors for ALT recovery included the time interval between ALT tests (days) and the group factor (bicyclol treatment). There were no differences in the proportion of renal function impairment or blood abnormalities between the two groups. CONCLUSIONS: Bicyclol is a potential candidate for DILI. SAGE Publications 2021-04-14 /pmc/articles/PMC8059044/ /pubmed/33853430 http://dx.doi.org/10.1177/03000605211005945 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Retrospective Clinical Research Report
Wang, Yongfeng
Lai, Rongtao
Zong, Peilan
Xu, Qingling
Shang, Jia
Zhang, Xia
Zhong, Wei
Tang, Jieting
Han, Xi’an
Chen, Chengwei
Mao, Yimin
Bicyclol for the treatment of drug-induced liver injury: a propensity score matching analysis using a nationwide inpatient database
title Bicyclol for the treatment of drug-induced liver injury: a propensity score matching analysis using a nationwide inpatient database
title_full Bicyclol for the treatment of drug-induced liver injury: a propensity score matching analysis using a nationwide inpatient database
title_fullStr Bicyclol for the treatment of drug-induced liver injury: a propensity score matching analysis using a nationwide inpatient database
title_full_unstemmed Bicyclol for the treatment of drug-induced liver injury: a propensity score matching analysis using a nationwide inpatient database
title_short Bicyclol for the treatment of drug-induced liver injury: a propensity score matching analysis using a nationwide inpatient database
title_sort bicyclol for the treatment of drug-induced liver injury: a propensity score matching analysis using a nationwide inpatient database
topic Retrospective Clinical Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8059044/
https://www.ncbi.nlm.nih.gov/pubmed/33853430
http://dx.doi.org/10.1177/03000605211005945
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