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Application of a biochemical and clinical model to predict individual survival in patients with end-stage liver disease

AIM: To investigate the capability of a biochemical and clinical model, BioCliM, in predicting the survival of cirrhotic patients. METHODS: We prospectively evaluated the survival of 172 cirrhotic patients. The model was constructed using clinical (ascites, encephalopathy and variceal bleeding) and...

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Published in:World journal of gastroenterology : WJG 2009-06, Vol.15 (22), p.2768-2777
Main Authors: Gomez, Eduardo Vilar, Bertot, Luis Calzadilla, Oramas, Bienvenido Gra, Soler, Enrique Arus, Navarro, Raimundo Llanio, Elias, Javier Diaz, Jiménez, Oscar Villa, Abreu Vazquez, Maria del Rosario
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cited_by cdi_FETCH-LOGICAL-c435t-beb58dc8e2fc1c84809f942c85f25b961bb5d9e55ea67c6a3bfb1df47798c4203
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container_title World journal of gastroenterology : WJG
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creator Gomez, Eduardo Vilar
Bertot, Luis Calzadilla
Oramas, Bienvenido Gra
Soler, Enrique Arus
Navarro, Raimundo Llanio
Elias, Javier Diaz
Jiménez, Oscar Villa
Abreu Vazquez, Maria del Rosario
description AIM: To investigate the capability of a biochemical and clinical model, BioCliM, in predicting the survival of cirrhotic patients. METHODS: We prospectively evaluated the survival of 172 cirrhotic patients. The model was constructed using clinical (ascites, encephalopathy and variceal bleeding) and biochemical (serum creatinine and serum total bilirubin) variables that were selected from a Cox proportional hazards model. It was applied to estimate 12-, 52- and 104-wk survival. The model's calibration using the Hosmer-Lemeshow statistic was computed at 104 wk in a validation dataset. Finally, the model's validity was tested among an independent set of 85 patients who were stratified into 2 risk groups (low risk ≤ 8 and high risk 〉 8).RESULTS: In the validation cohort, all measures of fit, discrimination and calibration were improved when the biochemical and clinical model was used. The proposed model had better predictive values (c-statistic: 0.90, 0.91, 0.91) than the Model for End-stage Liver Disease (MELD) and Child-Pugh (CP) scores for 12-, 52- and 104-wk mortality, respectively. In addition, the Hosmer-Lemeshow (H-L) statistic revealed that the biochemical and clinical model (H-L, 4.69) is better calibrated than MELD (H-L, 17.06) and CP (H-L, 14.23). There were no significant differences between the observed and expected survival curves in the stratified risk groups (low risk, P = 0.61; high risk, P = 0.77). CONCLUSION: Our data suggest that the proposed model is able to accurately predict survival in cirrhotic patients.
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METHODS: We prospectively evaluated the survival of 172 cirrhotic patients. The model was constructed using clinical (ascites, encephalopathy and variceal bleeding) and biochemical (serum creatinine and serum total bilirubin) variables that were selected from a Cox proportional hazards model. It was applied to estimate 12-, 52- and 104-wk survival. The model's calibration using the Hosmer-Lemeshow statistic was computed at 104 wk in a validation dataset. Finally, the model's validity was tested among an independent set of 85 patients who were stratified into 2 risk groups (low risk ≤ 8 and high risk 〉 8).RESULTS: In the validation cohort, all measures of fit, discrimination and calibration were improved when the biochemical and clinical model was used. The proposed model had better predictive values (c-statistic: 0.90, 0.91, 0.91) than the Model for End-stage Liver Disease (MELD) and Child-Pugh (CP) scores for 12-, 52- and 104-wk mortality, respectively. In addition, the Hosmer-Lemeshow (H-L) statistic revealed that the biochemical and clinical model (H-L, 4.69) is better calibrated than MELD (H-L, 17.06) and CP (H-L, 14.23). There were no significant differences between the observed and expected survival curves in the stratified risk groups (low risk, P = 0.61; high risk, P = 0.77). CONCLUSION: Our data suggest that the proposed model is able to accurately predict survival in cirrhotic patients.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.15.2768</identifier><identifier>PMID: 19522028</identifier><language>eng</language><publisher>United States: Department of Hepatology,National Institute of Gastroenterology,Havana 10400,Cuba%Department of Pathology,National Institute of Gastroenterology,Havana 10400,Cuba%Department of Gastroenterology,National Institute of Gastroenterology,Havana 10400,Cuba%Deparment of Gastroenterology,The "Calixto Garcia" Hospital,Havana 10400,Cuba Oscar%Department of Biostatistics,National Institute of Gastroenterology,Havana 10400,Cuba</publisher><subject>Adult ; Aged ; Brief ; Female ; Humans ; Liver Failure - diagnosis ; Liver Failure - mortality ; Male ; Middle Aged ; Models, Biological ; Multivariate Analysis ; Prognosis ; Proportional Hazards Models ; Prospective Studies ; Reproducibility of Results ; Risk Factors ; Young Adult ; 模型预测</subject><ispartof>World journal of gastroenterology : WJG, 2009-06, Vol.15 (22), p.2768-2777</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><rights>2009 The WJG Press and Baishideng. All rights reserved. 2009</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-beb58dc8e2fc1c84809f942c85f25b961bb5d9e55ea67c6a3bfb1df47798c4203</citedby><cites>FETCH-LOGICAL-c435t-beb58dc8e2fc1c84809f942c85f25b961bb5d9e55ea67c6a3bfb1df47798c4203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695893/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695893/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19522028$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gomez, Eduardo Vilar</creatorcontrib><creatorcontrib>Bertot, Luis Calzadilla</creatorcontrib><creatorcontrib>Oramas, Bienvenido Gra</creatorcontrib><creatorcontrib>Soler, Enrique Arus</creatorcontrib><creatorcontrib>Navarro, Raimundo Llanio</creatorcontrib><creatorcontrib>Elias, Javier Diaz</creatorcontrib><creatorcontrib>Jiménez, Oscar Villa</creatorcontrib><creatorcontrib>Abreu Vazquez, Maria del Rosario</creatorcontrib><title>Application of a biochemical and clinical model to predict individual survival in patients with end-stage liver disease</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM: To investigate the capability of a biochemical and clinical model, BioCliM, in predicting the survival of cirrhotic patients. 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METHODS: We prospectively evaluated the survival of 172 cirrhotic patients. The model was constructed using clinical (ascites, encephalopathy and variceal bleeding) and biochemical (serum creatinine and serum total bilirubin) variables that were selected from a Cox proportional hazards model. It was applied to estimate 12-, 52- and 104-wk survival. The model's calibration using the Hosmer-Lemeshow statistic was computed at 104 wk in a validation dataset. Finally, the model's validity was tested among an independent set of 85 patients who were stratified into 2 risk groups (low risk ≤ 8 and high risk 〉 8).RESULTS: In the validation cohort, all measures of fit, discrimination and calibration were improved when the biochemical and clinical model was used. The proposed model had better predictive values (c-statistic: 0.90, 0.91, 0.91) than the Model for End-stage Liver Disease (MELD) and Child-Pugh (CP) scores for 12-, 52- and 104-wk mortality, respectively. In addition, the Hosmer-Lemeshow (H-L) statistic revealed that the biochemical and clinical model (H-L, 4.69) is better calibrated than MELD (H-L, 17.06) and CP (H-L, 14.23). There were no significant differences between the observed and expected survival curves in the stratified risk groups (low risk, P = 0.61; high risk, P = 0.77). 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subjects Adult
Aged
Brief
Female
Humans
Liver Failure - diagnosis
Liver Failure - mortality
Male
Middle Aged
Models, Biological
Multivariate Analysis
Prognosis
Proportional Hazards Models
Prospective Studies
Reproducibility of Results
Risk Factors
Young Adult
模型预测
title Application of a biochemical and clinical model to predict individual survival in patients with end-stage liver disease
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