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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 |
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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. 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><subject>Adult</subject><subject>Aged</subject><subject>Brief</subject><subject>Female</subject><subject>Humans</subject><subject>Liver Failure - diagnosis</subject><subject>Liver Failure - mortality</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Models, Biological</subject><subject>Multivariate Analysis</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Prospective Studies</subject><subject>Reproducibility of Results</subject><subject>Risk Factors</subject><subject>Young Adult</subject><subject>模型预测</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNpVkcmLFDEUh4MoTjt68i5BxItUm6VSlVwGhsENBrzoOWStTptOaipV1fjfm7Ybl1OW9-N7H-8B8BKjLe1b_v64H7aYbUnf8UdgQwgWDeEtegw2GKG-EZT0V-BZKXuECKWMPAVXWDBCEOEbcLwdxxiMmkNOMHuooA7Z7Nyh_kWokoUmhvT7ccjWRThnOE7OBjPDkGxYg11qrSzTGtZ6CQmOFebSXOAxzDvokm3KrAYHY1jdBG0oThX3HDzxKhb34nJeg-8fP3y7-9zcf_305e72vjEtZXOjnWbcGu6IN9jwliPhRUsMZ54wLTqsNbPCMeZU15tOUe01tr7te8FNSxC9Bjdn7rjog7Omik0qynEKBzX9lFkF-X8lhZ0c8ipJJxgXtALenAFHlbxKg9znZUpVWda5E4REHSQmNfb20mfKD4srszyEYlyMKrm8FNn1tONYnITenYNmyqVMzv9xwUie9nniSszkaZ81_epf_b_ZywJr4PUFt8tpeAhVUCvzw4foJEW8ZV3t_Au2Rao-</recordid><startdate>20090614</startdate><enddate>20090614</enddate><creator>Gomez, Eduardo Vilar</creator><creator>Bertot, Luis Calzadilla</creator><creator>Oramas, Bienvenido Gra</creator><creator>Soler, Enrique Arus</creator><creator>Navarro, Raimundo Llanio</creator><creator>Elias, Javier Diaz</creator><creator>Jiménez, Oscar Villa</creator><creator>Abreu Vazquez, Maria del Rosario</creator><general>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</general><general>The WJG Press and Baishideng</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W92</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope><scope>5PM</scope></search><sort><creationdate>20090614</creationdate><title>Application of a biochemical and clinical model to predict individual survival in patients with end-stage liver disease</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-beb58dc8e2fc1c84809f942c85f25b961bb5d9e55ea67c6a3bfb1df47798c4203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Brief</topic><topic>Female</topic><topic>Humans</topic><topic>Liver Failure - diagnosis</topic><topic>Liver Failure - mortality</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Models, Biological</topic><topic>Multivariate Analysis</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Prospective Studies</topic><topic>Reproducibility of Results</topic><topic>Risk Factors</topic><topic>Young Adult</topic><topic>模型预测</topic><toplevel>online_resources</toplevel><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><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-工程技术</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastroenterology : WJG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gomez, Eduardo Vilar</au><au>Bertot, Luis Calzadilla</au><au>Oramas, Bienvenido Gra</au><au>Soler, Enrique Arus</au><au>Navarro, Raimundo Llanio</au><au>Elias, Javier Diaz</au><au>Jiménez, Oscar Villa</au><au>Abreu Vazquez, Maria del Rosario</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of a biochemical and clinical model to predict individual survival in patients with end-stage liver disease</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World Journal of Gastroenterology</addtitle><date>2009-06-14</date><risdate>2009</risdate><volume>15</volume><issue>22</issue><spage>2768</spage><epage>2777</epage><pages>2768-2777</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>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.</abstract><cop>United States</cop><pub>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</pub><pmid>19522028</pmid><doi>10.3748/wjg.15.2768</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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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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