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Risk factors for hepatic veno-occlusive disease caused by Gynura segetum: a retrospective study

BACKGROUND: Hepatic veno-occlusive disease (HVOD) caused by Gynura segetum has been increasingly reported in China in recent years. The aim of this retrospective study was to identify independent prognostic markers for survival in patients with Gynura segetum-induced HVOD and to evaluate the effect...

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Autores principales: Wang, Yan, Qiao, Dan, Li, Ya, Xu, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204041/
https://www.ncbi.nlm.nih.gov/pubmed/30367628
http://dx.doi.org/10.1186/s12876-018-0879-7
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author Wang, Yan
Qiao, Dan
Li, Ya
Xu, Feng
author_facet Wang, Yan
Qiao, Dan
Li, Ya
Xu, Feng
author_sort Wang, Yan
collection PubMed
description BACKGROUND: Hepatic veno-occlusive disease (HVOD) caused by Gynura segetum has been increasingly reported in China in recent years. The aim of this retrospective study was to identify independent prognostic markers for survival in patients with Gynura segetum-induced HVOD and to evaluate the effect of anticoagulants and transjugular intrahepatic portosystemic shunt (TIPS) on survival rate. METHODS: Clinical data including symptoms, signs, imaging characteristics, laboratory test results, results of liver tissue biopsies, type of treatment during follow-up and clinical outcomes were collected. Univariate, multivariate and time-dependent Cox regression analyses were performed. RESULTS: Survival rates were 91% (95% confidence interval [CI], 82–95%), 64% (95% CI, 53–69%) and 57% (95% CI, 51–65%) at 1, 3 and 60 months, respectively. Total bilirubin, albumin and hepatic encephalopathy were independent prognostic markers of survival. Anticoagulants were administered to 76% of the patients. Among 75 patients treated with anticoagulants, 49 patients (65.3%) were cured, whereas 26 patients (34.7%) died; the cure rate in anticoagulant-treated patients was higher than that of those not treated with anticoagulants (χ(2) = 9.129, P = 0.004). Cure rate of the anticoagulation + TIPS treatment group was 64.3%, which was also higher than that of the non-anticoagulation group; however, this was not significantly different (χ(2) = 3.938, P = 0.096). CONCLUSIONS: The presence of hepatic encephalopathy, serum bilirubin and albumin levels were major prognostic factors for Gynura segetum-induced HVOD. Anticoagulation therapy significantly increased the cure rate; however, TIPS treatment did not have a beneficial effect on the cure rate.
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spelling pubmed-62040412018-11-01 Risk factors for hepatic veno-occlusive disease caused by Gynura segetum: a retrospective study Wang, Yan Qiao, Dan Li, Ya Xu, Feng BMC Gastroenterol Research Article BACKGROUND: Hepatic veno-occlusive disease (HVOD) caused by Gynura segetum has been increasingly reported in China in recent years. The aim of this retrospective study was to identify independent prognostic markers for survival in patients with Gynura segetum-induced HVOD and to evaluate the effect of anticoagulants and transjugular intrahepatic portosystemic shunt (TIPS) on survival rate. METHODS: Clinical data including symptoms, signs, imaging characteristics, laboratory test results, results of liver tissue biopsies, type of treatment during follow-up and clinical outcomes were collected. Univariate, multivariate and time-dependent Cox regression analyses were performed. RESULTS: Survival rates were 91% (95% confidence interval [CI], 82–95%), 64% (95% CI, 53–69%) and 57% (95% CI, 51–65%) at 1, 3 and 60 months, respectively. Total bilirubin, albumin and hepatic encephalopathy were independent prognostic markers of survival. Anticoagulants were administered to 76% of the patients. Among 75 patients treated with anticoagulants, 49 patients (65.3%) were cured, whereas 26 patients (34.7%) died; the cure rate in anticoagulant-treated patients was higher than that of those not treated with anticoagulants (χ(2) = 9.129, P = 0.004). Cure rate of the anticoagulation + TIPS treatment group was 64.3%, which was also higher than that of the non-anticoagulation group; however, this was not significantly different (χ(2) = 3.938, P = 0.096). CONCLUSIONS: The presence of hepatic encephalopathy, serum bilirubin and albumin levels were major prognostic factors for Gynura segetum-induced HVOD. Anticoagulation therapy significantly increased the cure rate; however, TIPS treatment did not have a beneficial effect on the cure rate. BioMed Central 2018-10-26 /pmc/articles/PMC6204041/ /pubmed/30367628 http://dx.doi.org/10.1186/s12876-018-0879-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wang, Yan
Qiao, Dan
Li, Ya
Xu, Feng
Risk factors for hepatic veno-occlusive disease caused by Gynura segetum: a retrospective study
title Risk factors for hepatic veno-occlusive disease caused by Gynura segetum: a retrospective study
title_full Risk factors for hepatic veno-occlusive disease caused by Gynura segetum: a retrospective study
title_fullStr Risk factors for hepatic veno-occlusive disease caused by Gynura segetum: a retrospective study
title_full_unstemmed Risk factors for hepatic veno-occlusive disease caused by Gynura segetum: a retrospective study
title_short Risk factors for hepatic veno-occlusive disease caused by Gynura segetum: a retrospective study
title_sort risk factors for hepatic veno-occlusive disease caused by gynura segetum: a retrospective study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204041/
https://www.ncbi.nlm.nih.gov/pubmed/30367628
http://dx.doi.org/10.1186/s12876-018-0879-7
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