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Progression of liver cirrhosis to HCC: an application of hidden Markov model

BACKGROUND: Health service databases of administrative type can be a useful tool for the study of progression of a disease, but the data reported in such sources could be affected by misclassifications of some patients' real disease states at the time. Aim of this work was to estimate the trans...

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Autores principales: Bartolomeo, Nicola, Trerotoli, Paolo, Serio, Gabriella
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3087702/
https://www.ncbi.nlm.nih.gov/pubmed/21457586
http://dx.doi.org/10.1186/1471-2288-11-38
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author Bartolomeo, Nicola
Trerotoli, Paolo
Serio, Gabriella
author_facet Bartolomeo, Nicola
Trerotoli, Paolo
Serio, Gabriella
author_sort Bartolomeo, Nicola
collection PubMed
description BACKGROUND: Health service databases of administrative type can be a useful tool for the study of progression of a disease, but the data reported in such sources could be affected by misclassifications of some patients' real disease states at the time. Aim of this work was to estimate the transition probabilities through the different degenerative phases of liver cirrhosis using health service databases. METHODS: We employed a hidden Markov model to determine the transition probabilities between two states, and of misclassification. The covariates inserted in the model were sex, age, the presence of comorbidities correlated with alcohol abuse, the presence of diagnosis codes indicating hepatitis C virus infection, and the Charlson Index. The analysis was conducted in patients presumed to have suffered the onset of cirrhosis in 2000, observing the disease evolution and, if applicable, death up to the end of the year 2006. RESULTS: The incidence of hepatocellular carcinoma (HCC) in cirrhotic patients was 1.5% per year. The probability of developing HCC is higher in males (OR = 2.217) and patients over 65 (OR = 1.547); over 65-year-olds have a greater probability of death both while still suffering from cirrhosis (OR = 2.379) and if they have developed HCC (OR = 1.410). A more severe casemix affects the transition from HCC to death (OR = 1.714). The probability of misclassifying subjects with HCC as exclusively affected by liver cirrhosis is 14.08%. CONCLUSIONS: The hidden Markov model allowing for misclassification is well suited to analyses of health service databases, since it is able to capture bias due to the fact that the quality and accuracy of the available information are not always optimal. The probability of evolution of a cirrhotic subject to HCC depends on sex and age class, while hepatitis C virus infection and comorbidities correlated with alcohol abuse do not seem to have an influence.
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spelling pubmed-30877022011-05-05 Progression of liver cirrhosis to HCC: an application of hidden Markov model Bartolomeo, Nicola Trerotoli, Paolo Serio, Gabriella BMC Med Res Methodol Research Article BACKGROUND: Health service databases of administrative type can be a useful tool for the study of progression of a disease, but the data reported in such sources could be affected by misclassifications of some patients' real disease states at the time. Aim of this work was to estimate the transition probabilities through the different degenerative phases of liver cirrhosis using health service databases. METHODS: We employed a hidden Markov model to determine the transition probabilities between two states, and of misclassification. The covariates inserted in the model were sex, age, the presence of comorbidities correlated with alcohol abuse, the presence of diagnosis codes indicating hepatitis C virus infection, and the Charlson Index. The analysis was conducted in patients presumed to have suffered the onset of cirrhosis in 2000, observing the disease evolution and, if applicable, death up to the end of the year 2006. RESULTS: The incidence of hepatocellular carcinoma (HCC) in cirrhotic patients was 1.5% per year. The probability of developing HCC is higher in males (OR = 2.217) and patients over 65 (OR = 1.547); over 65-year-olds have a greater probability of death both while still suffering from cirrhosis (OR = 2.379) and if they have developed HCC (OR = 1.410). A more severe casemix affects the transition from HCC to death (OR = 1.714). The probability of misclassifying subjects with HCC as exclusively affected by liver cirrhosis is 14.08%. CONCLUSIONS: The hidden Markov model allowing for misclassification is well suited to analyses of health service databases, since it is able to capture bias due to the fact that the quality and accuracy of the available information are not always optimal. The probability of evolution of a cirrhotic subject to HCC depends on sex and age class, while hepatitis C virus infection and comorbidities correlated with alcohol abuse do not seem to have an influence. BioMed Central 2011-04-04 /pmc/articles/PMC3087702/ /pubmed/21457586 http://dx.doi.org/10.1186/1471-2288-11-38 Text en Copyright ©2011 Bartolomeo et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bartolomeo, Nicola
Trerotoli, Paolo
Serio, Gabriella
Progression of liver cirrhosis to HCC: an application of hidden Markov model
title Progression of liver cirrhosis to HCC: an application of hidden Markov model
title_full Progression of liver cirrhosis to HCC: an application of hidden Markov model
title_fullStr Progression of liver cirrhosis to HCC: an application of hidden Markov model
title_full_unstemmed Progression of liver cirrhosis to HCC: an application of hidden Markov model
title_short Progression of liver cirrhosis to HCC: an application of hidden Markov model
title_sort progression of liver cirrhosis to hcc: an application of hidden markov model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3087702/
https://www.ncbi.nlm.nih.gov/pubmed/21457586
http://dx.doi.org/10.1186/1471-2288-11-38
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