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Development and evaluation of a baseline-event-anticipation score for hepatitis delta

Hepatitis delta is considered the most severe form of viral hepatitis, but variables associated with disease progression are poorly defined. This study aimed to identify risk factors associated with worse clinical outcome in patients with hepatitis delta and to develop a clinical score to determine...

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Autores principales: Calle Serrano, B, Großhennig, A, Homs, M, Heidrich, B, Erhardt, A, Deterding, K, Jaroszewicz, J, Bremer, B, Koch, A, Cornberg, M, Manns, M P, Buti, M, Wedemeyer, H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4263246/
https://www.ncbi.nlm.nih.gov/pubmed/24673975
http://dx.doi.org/10.1111/jvh.12251
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author Calle Serrano, B
Großhennig, A
Homs, M
Heidrich, B
Erhardt, A
Deterding, K
Jaroszewicz, J
Bremer, B
Koch, A
Cornberg, M
Manns, M P
Buti, M
Wedemeyer, H
author_facet Calle Serrano, B
Großhennig, A
Homs, M
Heidrich, B
Erhardt, A
Deterding, K
Jaroszewicz, J
Bremer, B
Koch, A
Cornberg, M
Manns, M P
Buti, M
Wedemeyer, H
author_sort Calle Serrano, B
collection PubMed
description Hepatitis delta is considered the most severe form of viral hepatitis, but variables associated with disease progression are poorly defined. This study aimed to identify risk factors associated with worse clinical outcome in patients with hepatitis delta and to develop a clinical score to determine their risk of experiencing liver-related morbidity or mortality. We followed 75 HBsAg–anti-HDV-positive patients with hepatitis delta for up to 16 years (median 5 years). The baseline-event-anticipation score (BEA score) was developed based on variables associated with the development of liver-related clinical complications. Age, region of origin, presence of cirrhosis, albumin, INR, hyperbilirubinemia and thrombocytopenia were all associated with the development of an event in the training cohort. The BEA score included age, sex, region of origin, bilirubin, platelets and INR. Points were allocated according to hazard ratios, and three risk groups were defined: BEA-A mild risk, BEA-B moderate risk and BEA-C high risk. Hazard ratios of BEA-B and BEA-C patients for liver-related clinical endpoints were 9.01 and 25.27 vs BEA-A with an area under curve of the receiving operating characteristic curve of 0.88. The accuracy of the BEA score was confirmed in two independent validation cohorts followed in Barcelona (n = 77) and Düsseldorf (n = 62). Delta hepatitis is associated with a very severe long-term outcome. The BEA score is easy to apply and predicts with a very high accuracy the development of liver-related complications in patients with hepatitis delta.
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spelling pubmed-42632462014-12-15 Development and evaluation of a baseline-event-anticipation score for hepatitis delta Calle Serrano, B Großhennig, A Homs, M Heidrich, B Erhardt, A Deterding, K Jaroszewicz, J Bremer, B Koch, A Cornberg, M Manns, M P Buti, M Wedemeyer, H J Viral Hepat Original Articles Hepatitis delta is considered the most severe form of viral hepatitis, but variables associated with disease progression are poorly defined. This study aimed to identify risk factors associated with worse clinical outcome in patients with hepatitis delta and to develop a clinical score to determine their risk of experiencing liver-related morbidity or mortality. We followed 75 HBsAg–anti-HDV-positive patients with hepatitis delta for up to 16 years (median 5 years). The baseline-event-anticipation score (BEA score) was developed based on variables associated with the development of liver-related clinical complications. Age, region of origin, presence of cirrhosis, albumin, INR, hyperbilirubinemia and thrombocytopenia were all associated with the development of an event in the training cohort. The BEA score included age, sex, region of origin, bilirubin, platelets and INR. Points were allocated according to hazard ratios, and three risk groups were defined: BEA-A mild risk, BEA-B moderate risk and BEA-C high risk. Hazard ratios of BEA-B and BEA-C patients for liver-related clinical endpoints were 9.01 and 25.27 vs BEA-A with an area under curve of the receiving operating characteristic curve of 0.88. The accuracy of the BEA score was confirmed in two independent validation cohorts followed in Barcelona (n = 77) and Düsseldorf (n = 62). Delta hepatitis is associated with a very severe long-term outcome. The BEA score is easy to apply and predicts with a very high accuracy the development of liver-related complications in patients with hepatitis delta. BlackWell Publishing Ltd 2014-11 2014-03-27 /pmc/articles/PMC4263246/ /pubmed/24673975 http://dx.doi.org/10.1111/jvh.12251 Text en © 2014 The Authors. Journal of Viral Hepatitis published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Calle Serrano, B
Großhennig, A
Homs, M
Heidrich, B
Erhardt, A
Deterding, K
Jaroszewicz, J
Bremer, B
Koch, A
Cornberg, M
Manns, M P
Buti, M
Wedemeyer, H
Development and evaluation of a baseline-event-anticipation score for hepatitis delta
title Development and evaluation of a baseline-event-anticipation score for hepatitis delta
title_full Development and evaluation of a baseline-event-anticipation score for hepatitis delta
title_fullStr Development and evaluation of a baseline-event-anticipation score for hepatitis delta
title_full_unstemmed Development and evaluation of a baseline-event-anticipation score for hepatitis delta
title_short Development and evaluation of a baseline-event-anticipation score for hepatitis delta
title_sort development and evaluation of a baseline-event-anticipation score for hepatitis delta
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4263246/
https://www.ncbi.nlm.nih.gov/pubmed/24673975
http://dx.doi.org/10.1111/jvh.12251
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