Risk Stratification Based on Chronic Liver Failure Consortium Acute Decompensation Score in Patients With Child‐Pugh B Cirrhosis and Acute Variceal Bleeding

Background and Aims Optimal candidates for early transjugular intrahepatic portosystemic shunt (TIPS) in patients with Child‐Pugh B cirrhosis and acute variceal bleeding (AVB) remain unclear. This study aimed to test the hypothesis that risk stratification using the Chronic Liver Failure Consortium...

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Veröffentlicht in:Hepatology (Baltimore, Md.) Md.), 2021-04, Vol.73 (4), p.1478-1493
Hauptverfasser: Lv, Yong, Wang, Zhengyu, Li, Kai, Wang, Qiuhe, Bai, Wei, Yuan, Xulong, Yu, Tianlei, Niu, Jing, Yang, Zhiping, Zhu, Xuan, Zhao, Jianbo, Xue, Hui, Jiang, Zaibo, Zhuge, Yuzheng, Zhang, Chunqing, Sun, Junhui, Ding, Pengxu, Ren, Weixin, Li, Yingchun, Zhang, Kewei, Zhang, Wenguang, Guo, Wengang, Luo, Bohan, Li, Xiaomei, Yuan, Jie, Han, Na, Zhu, Ying, He, Chuangye, Yin, Zhanxin, Fan, Daiming, Han, Guohong
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container_issue 4
container_start_page 1478
container_title Hepatology (Baltimore, Md.)
container_volume 73
creator Lv, Yong
Wang, Zhengyu
Li, Kai
Wang, Qiuhe
Bai, Wei
Yuan, Xulong
Yu, Tianlei
Niu, Jing
Yang, Zhiping
Zhu, Xuan
Zhao, Jianbo
Xue, Hui
Jiang, Zaibo
Zhuge, Yuzheng
Zhang, Chunqing
Sun, Junhui
Ding, Pengxu
Ren, Weixin
Li, Yingchun
Zhang, Kewei
Zhang, Wenguang
Guo, Wengang
Luo, Bohan
Li, Xiaomei
Yuan, Jie
Han, Na
Zhu, Ying
He, Chuangye
Yin, Zhanxin
Fan, Daiming
Han, Guohong
description Background and Aims Optimal candidates for early transjugular intrahepatic portosystemic shunt (TIPS) in patients with Child‐Pugh B cirrhosis and acute variceal bleeding (AVB) remain unclear. This study aimed to test the hypothesis that risk stratification using the Chronic Liver Failure Consortium Acute Decompensation score (CLIF‐C ADs) may be useful to identify a subgroup at high risk of mortality or further bleeding that may benefit from early TIPS in patients with Child‐Pugh B cirrhosis and AVB. Approach and Results We analyzed the pooled individual data from two previous studies of 608 patients with Child‐Pugh B cirrhosis and AVB who received standard treatment between 2010 and 2017 in China. The concordance index values of CLIF‐C ADs for 6‐week and 1‐year mortality (0.715 and 0.708) were significantly better than those of active bleeding at endoscopy (0.633 [P 
doi_str_mv 10.1002/hep.31478
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This study aimed to test the hypothesis that risk stratification using the Chronic Liver Failure Consortium Acute Decompensation score (CLIF‐C ADs) may be useful to identify a subgroup at high risk of mortality or further bleeding that may benefit from early TIPS in patients with Child‐Pugh B cirrhosis and AVB. Approach and Results We analyzed the pooled individual data from two previous studies of 608 patients with Child‐Pugh B cirrhosis and AVB who received standard treatment between 2010 and 2017 in China. The concordance index values of CLIF‐C ADs for 6‐week and 1‐year mortality (0.715 and 0.708) were significantly better than those of active bleeding at endoscopy (0.633 [P &lt; 0.001] and 0.556 [P &lt; 0.001]) and other prognostic models. With X‐tile software identifying an optimal cutoff value, patients were categorized as low risk (CLIF‐C ADs &lt;48), intermediate risk (CLIF‐C ADs 48‐56), and high risk (CLIF‐C ADs &gt;56), with a 5.6%, 16.8%, and 25.4% risk of 6‐week death, respectively. Nevertheless, the performance of CLIF‐C ADs for predicting a composite endpoint of 6‐week death or further bleeding was not satisfactory (area under the receiver operating characteristics curve [AUC], 0.588). A nomogram incorporating components of CLIF‐C ADs and albumin, platelet, active bleeding, and ascites significantly improved the prediction accuracy (AUC, 0.725). Conclusions In patients with Child‐Pugh B cirrhosis and AVB, risk stratification using CLIF‐C ADs identifies a subgroup with high risk of death that may derive survival benefit from early TIPS. With improved prediction accuracy for 6‐week death or further bleeding, the data‐driven nomogram may help to stratify patients in randomized trials. Future external validation of these findings in patients with different etiologies is required.</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.31478</identifier><identifier>PMID: 32706906</identifier><language>eng</language><publisher>United States: Wolters Kluwer Health, Inc</publisher><subject>Acute Disease - epidemiology ; Acute-On-Chronic Liver Failure ; Adult ; Aged ; Ascites ; Bleeding ; China - epidemiology ; Cirrhosis ; Clinical trials ; Comorbidity ; Consortia ; Death ; Endoscopy ; Esophageal and Gastric Varices - epidemiology ; Esophageal and Gastric Varices - mortality ; Esophageal and Gastric Varices - surgery ; Female ; Follow-Up Studies ; Gastrointestinal Hemorrhage - epidemiology ; Gastrointestinal Hemorrhage - mortality ; Gastrointestinal Hemorrhage - surgery ; Hepatology ; Humans ; Liver cirrhosis ; Liver Cirrhosis - epidemiology ; Liver failure ; Male ; Middle Aged ; Mortality ; Nomograms ; Portasystemic Shunt, Transjugular Intrahepatic - methods ; Prognosis ; Prospective Studies ; Research Design ; Retrospective Studies ; Risk Assessment ; Treatment Outcome</subject><ispartof>Hepatology (Baltimore, Md.), 2021-04, Vol.73 (4), p.1478-1493</ispartof><rights>2020 by the American Association for the Study of Liver Diseases.</rights><rights>2021 by the American Association for the Study of Liver Diseases.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3538-120664fc01b257fac6133ec6b2188cb062b5b1237f070a26b571b4bfdef72e3f3</citedby><cites>FETCH-LOGICAL-c3538-120664fc01b257fac6133ec6b2188cb062b5b1237f070a26b571b4bfdef72e3f3</cites><orcidid>0000-0003-4568-3776</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhep.31478$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhep.31478$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32706906$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lv, Yong</creatorcontrib><creatorcontrib>Wang, Zhengyu</creatorcontrib><creatorcontrib>Li, Kai</creatorcontrib><creatorcontrib>Wang, Qiuhe</creatorcontrib><creatorcontrib>Bai, Wei</creatorcontrib><creatorcontrib>Yuan, Xulong</creatorcontrib><creatorcontrib>Yu, Tianlei</creatorcontrib><creatorcontrib>Niu, Jing</creatorcontrib><creatorcontrib>Yang, Zhiping</creatorcontrib><creatorcontrib>Zhu, Xuan</creatorcontrib><creatorcontrib>Zhao, Jianbo</creatorcontrib><creatorcontrib>Xue, Hui</creatorcontrib><creatorcontrib>Jiang, Zaibo</creatorcontrib><creatorcontrib>Zhuge, Yuzheng</creatorcontrib><creatorcontrib>Zhang, Chunqing</creatorcontrib><creatorcontrib>Sun, Junhui</creatorcontrib><creatorcontrib>Ding, Pengxu</creatorcontrib><creatorcontrib>Ren, Weixin</creatorcontrib><creatorcontrib>Li, Yingchun</creatorcontrib><creatorcontrib>Zhang, Kewei</creatorcontrib><creatorcontrib>Zhang, Wenguang</creatorcontrib><creatorcontrib>Guo, Wengang</creatorcontrib><creatorcontrib>Luo, Bohan</creatorcontrib><creatorcontrib>Li, Xiaomei</creatorcontrib><creatorcontrib>Yuan, Jie</creatorcontrib><creatorcontrib>Han, Na</creatorcontrib><creatorcontrib>Zhu, Ying</creatorcontrib><creatorcontrib>He, Chuangye</creatorcontrib><creatorcontrib>Yin, Zhanxin</creatorcontrib><creatorcontrib>Fan, Daiming</creatorcontrib><creatorcontrib>Han, Guohong</creatorcontrib><title>Risk Stratification Based on Chronic Liver Failure Consortium Acute Decompensation Score in Patients With Child‐Pugh B Cirrhosis and Acute Variceal Bleeding</title><title>Hepatology (Baltimore, Md.)</title><addtitle>Hepatology</addtitle><description>Background and Aims Optimal candidates for early transjugular intrahepatic portosystemic shunt (TIPS) in patients with Child‐Pugh B cirrhosis and acute variceal bleeding (AVB) remain unclear. This study aimed to test the hypothesis that risk stratification using the Chronic Liver Failure Consortium Acute Decompensation score (CLIF‐C ADs) may be useful to identify a subgroup at high risk of mortality or further bleeding that may benefit from early TIPS in patients with Child‐Pugh B cirrhosis and AVB. Approach and Results We analyzed the pooled individual data from two previous studies of 608 patients with Child‐Pugh B cirrhosis and AVB who received standard treatment between 2010 and 2017 in China. The concordance index values of CLIF‐C ADs for 6‐week and 1‐year mortality (0.715 and 0.708) were significantly better than those of active bleeding at endoscopy (0.633 [P &lt; 0.001] and 0.556 [P &lt; 0.001]) and other prognostic models. With X‐tile software identifying an optimal cutoff value, patients were categorized as low risk (CLIF‐C ADs &lt;48), intermediate risk (CLIF‐C ADs 48‐56), and high risk (CLIF‐C ADs &gt;56), with a 5.6%, 16.8%, and 25.4% risk of 6‐week death, respectively. Nevertheless, the performance of CLIF‐C ADs for predicting a composite endpoint of 6‐week death or further bleeding was not satisfactory (area under the receiver operating characteristics curve [AUC], 0.588). A nomogram incorporating components of CLIF‐C ADs and albumin, platelet, active bleeding, and ascites significantly improved the prediction accuracy (AUC, 0.725). Conclusions In patients with Child‐Pugh B cirrhosis and AVB, risk stratification using CLIF‐C ADs identifies a subgroup with high risk of death that may derive survival benefit from early TIPS. With improved prediction accuracy for 6‐week death or further bleeding, the data‐driven nomogram may help to stratify patients in randomized trials. Future external validation of these findings in patients with different etiologies is required.</description><subject>Acute Disease - epidemiology</subject><subject>Acute-On-Chronic Liver Failure</subject><subject>Adult</subject><subject>Aged</subject><subject>Ascites</subject><subject>Bleeding</subject><subject>China - epidemiology</subject><subject>Cirrhosis</subject><subject>Clinical trials</subject><subject>Comorbidity</subject><subject>Consortia</subject><subject>Death</subject><subject>Endoscopy</subject><subject>Esophageal and Gastric Varices - epidemiology</subject><subject>Esophageal and Gastric Varices - mortality</subject><subject>Esophageal and Gastric Varices - surgery</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gastrointestinal Hemorrhage - epidemiology</subject><subject>Gastrointestinal Hemorrhage - mortality</subject><subject>Gastrointestinal Hemorrhage - surgery</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Liver cirrhosis</subject><subject>Liver Cirrhosis - epidemiology</subject><subject>Liver failure</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Nomograms</subject><subject>Portasystemic Shunt, Transjugular Intrahepatic - methods</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Research Design</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Treatment Outcome</subject><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1u1DAQxy0EokvhwAsgS1zgkNYfiZ0cu6GllVbqivJxtBxn0rgk9mInoN54BJ6Ah-NJasjSAxIXj0fzm59G-iP0nJIjSgg77mF3xGkuywdoRQsmM84L8hCtCJMkqyivDtCTGG8IIVXOysfogKeBqIhYoZ_vbPyMr6agJ9tZk17v8FpHaHH61H3wzhq8sV8h4DNthzkArr2LPkx2HvGJmSfAb8D4cQcuLutXxifKOrxNPbgp4k926pPMDu2v7z-283WP17i2IfQ-2oi1a_eijzpYA3rA6wGgte76KXrU6SHCs309RB_OTt_X59nm8u1FfbLJDC94mVFGhMg7Q2jDCtlpIyjnYETDaFmahgjWFA1lXHZEEs1EU0ja5E3XQicZ8I4foleLdxf8lxnipEYbDQyDduDnqFjOJKuk5CyhL_9Bb_wcXLpOsYIyKqSgNFGvF8oEH2OATu2CHXW4VZSo36GpFJr6E1piX-yNczNCe0_-TSkBxwvwzQ5w-3-TOj_dLso74ASiRA</recordid><startdate>202104</startdate><enddate>202104</enddate><creator>Lv, Yong</creator><creator>Wang, Zhengyu</creator><creator>Li, Kai</creator><creator>Wang, Qiuhe</creator><creator>Bai, Wei</creator><creator>Yuan, Xulong</creator><creator>Yu, Tianlei</creator><creator>Niu, Jing</creator><creator>Yang, Zhiping</creator><creator>Zhu, Xuan</creator><creator>Zhao, Jianbo</creator><creator>Xue, Hui</creator><creator>Jiang, Zaibo</creator><creator>Zhuge, Yuzheng</creator><creator>Zhang, Chunqing</creator><creator>Sun, Junhui</creator><creator>Ding, Pengxu</creator><creator>Ren, Weixin</creator><creator>Li, Yingchun</creator><creator>Zhang, Kewei</creator><creator>Zhang, Wenguang</creator><creator>Guo, Wengang</creator><creator>Luo, Bohan</creator><creator>Li, Xiaomei</creator><creator>Yuan, Jie</creator><creator>Han, Na</creator><creator>Zhu, Ying</creator><creator>He, Chuangye</creator><creator>Yin, Zhanxin</creator><creator>Fan, Daiming</creator><creator>Han, Guohong</creator><general>Wolters Kluwer Health, Inc</general><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>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4568-3776</orcidid></search><sort><creationdate>202104</creationdate><title>Risk Stratification Based on Chronic Liver Failure Consortium Acute Decompensation Score in Patients With Child‐Pugh B Cirrhosis and Acute Variceal Bleeding</title><author>Lv, Yong ; Wang, Zhengyu ; Li, Kai ; Wang, Qiuhe ; Bai, Wei ; Yuan, Xulong ; Yu, Tianlei ; Niu, Jing ; Yang, Zhiping ; Zhu, Xuan ; Zhao, Jianbo ; Xue, Hui ; Jiang, Zaibo ; Zhuge, Yuzheng ; Zhang, Chunqing ; Sun, Junhui ; Ding, Pengxu ; Ren, Weixin ; Li, Yingchun ; Zhang, Kewei ; Zhang, Wenguang ; Guo, Wengang ; Luo, Bohan ; Li, Xiaomei ; Yuan, Jie ; Han, Na ; Zhu, Ying ; He, Chuangye ; Yin, Zhanxin ; Fan, Daiming ; Han, Guohong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3538-120664fc01b257fac6133ec6b2188cb062b5b1237f070a26b571b4bfdef72e3f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acute Disease - epidemiology</topic><topic>Acute-On-Chronic Liver Failure</topic><topic>Adult</topic><topic>Aged</topic><topic>Ascites</topic><topic>Bleeding</topic><topic>China - epidemiology</topic><topic>Cirrhosis</topic><topic>Clinical trials</topic><topic>Comorbidity</topic><topic>Consortia</topic><topic>Death</topic><topic>Endoscopy</topic><topic>Esophageal and Gastric Varices - epidemiology</topic><topic>Esophageal and Gastric Varices - mortality</topic><topic>Esophageal and Gastric Varices - surgery</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gastrointestinal Hemorrhage - epidemiology</topic><topic>Gastrointestinal Hemorrhage - mortality</topic><topic>Gastrointestinal Hemorrhage - surgery</topic><topic>Hepatology</topic><topic>Humans</topic><topic>Liver cirrhosis</topic><topic>Liver Cirrhosis - epidemiology</topic><topic>Liver failure</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Nomograms</topic><topic>Portasystemic Shunt, Transjugular Intrahepatic - methods</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Research Design</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lv, Yong</creatorcontrib><creatorcontrib>Wang, Zhengyu</creatorcontrib><creatorcontrib>Li, Kai</creatorcontrib><creatorcontrib>Wang, Qiuhe</creatorcontrib><creatorcontrib>Bai, Wei</creatorcontrib><creatorcontrib>Yuan, Xulong</creatorcontrib><creatorcontrib>Yu, Tianlei</creatorcontrib><creatorcontrib>Niu, Jing</creatorcontrib><creatorcontrib>Yang, Zhiping</creatorcontrib><creatorcontrib>Zhu, Xuan</creatorcontrib><creatorcontrib>Zhao, Jianbo</creatorcontrib><creatorcontrib>Xue, Hui</creatorcontrib><creatorcontrib>Jiang, Zaibo</creatorcontrib><creatorcontrib>Zhuge, Yuzheng</creatorcontrib><creatorcontrib>Zhang, Chunqing</creatorcontrib><creatorcontrib>Sun, Junhui</creatorcontrib><creatorcontrib>Ding, Pengxu</creatorcontrib><creatorcontrib>Ren, Weixin</creatorcontrib><creatorcontrib>Li, Yingchun</creatorcontrib><creatorcontrib>Zhang, Kewei</creatorcontrib><creatorcontrib>Zhang, Wenguang</creatorcontrib><creatorcontrib>Guo, Wengang</creatorcontrib><creatorcontrib>Luo, Bohan</creatorcontrib><creatorcontrib>Li, Xiaomei</creatorcontrib><creatorcontrib>Yuan, Jie</creatorcontrib><creatorcontrib>Han, Na</creatorcontrib><creatorcontrib>Zhu, Ying</creatorcontrib><creatorcontrib>He, Chuangye</creatorcontrib><creatorcontrib>Yin, Zhanxin</creatorcontrib><creatorcontrib>Fan, Daiming</creatorcontrib><creatorcontrib>Han, Guohong</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Hepatology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lv, Yong</au><au>Wang, Zhengyu</au><au>Li, Kai</au><au>Wang, Qiuhe</au><au>Bai, Wei</au><au>Yuan, Xulong</au><au>Yu, Tianlei</au><au>Niu, Jing</au><au>Yang, Zhiping</au><au>Zhu, Xuan</au><au>Zhao, Jianbo</au><au>Xue, Hui</au><au>Jiang, Zaibo</au><au>Zhuge, Yuzheng</au><au>Zhang, Chunqing</au><au>Sun, Junhui</au><au>Ding, Pengxu</au><au>Ren, Weixin</au><au>Li, Yingchun</au><au>Zhang, Kewei</au><au>Zhang, Wenguang</au><au>Guo, Wengang</au><au>Luo, Bohan</au><au>Li, Xiaomei</au><au>Yuan, Jie</au><au>Han, Na</au><au>Zhu, Ying</au><au>He, Chuangye</au><au>Yin, Zhanxin</au><au>Fan, Daiming</au><au>Han, Guohong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk Stratification Based on Chronic Liver Failure Consortium Acute Decompensation Score in Patients With Child‐Pugh B Cirrhosis and Acute Variceal Bleeding</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><addtitle>Hepatology</addtitle><date>2021-04</date><risdate>2021</risdate><volume>73</volume><issue>4</issue><spage>1478</spage><epage>1493</epage><pages>1478-1493</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><abstract>Background and Aims Optimal candidates for early transjugular intrahepatic portosystemic shunt (TIPS) in patients with Child‐Pugh B cirrhosis and acute variceal bleeding (AVB) remain unclear. This study aimed to test the hypothesis that risk stratification using the Chronic Liver Failure Consortium Acute Decompensation score (CLIF‐C ADs) may be useful to identify a subgroup at high risk of mortality or further bleeding that may benefit from early TIPS in patients with Child‐Pugh B cirrhosis and AVB. Approach and Results We analyzed the pooled individual data from two previous studies of 608 patients with Child‐Pugh B cirrhosis and AVB who received standard treatment between 2010 and 2017 in China. The concordance index values of CLIF‐C ADs for 6‐week and 1‐year mortality (0.715 and 0.708) were significantly better than those of active bleeding at endoscopy (0.633 [P &lt; 0.001] and 0.556 [P &lt; 0.001]) and other prognostic models. With X‐tile software identifying an optimal cutoff value, patients were categorized as low risk (CLIF‐C ADs &lt;48), intermediate risk (CLIF‐C ADs 48‐56), and high risk (CLIF‐C ADs &gt;56), with a 5.6%, 16.8%, and 25.4% risk of 6‐week death, respectively. Nevertheless, the performance of CLIF‐C ADs for predicting a composite endpoint of 6‐week death or further bleeding was not satisfactory (area under the receiver operating characteristics curve [AUC], 0.588). A nomogram incorporating components of CLIF‐C ADs and albumin, platelet, active bleeding, and ascites significantly improved the prediction accuracy (AUC, 0.725). Conclusions In patients with Child‐Pugh B cirrhosis and AVB, risk stratification using CLIF‐C ADs identifies a subgroup with high risk of death that may derive survival benefit from early TIPS. With improved prediction accuracy for 6‐week death or further bleeding, the data‐driven nomogram may help to stratify patients in randomized trials. Future external validation of these findings in patients with different etiologies is required.</abstract><cop>United States</cop><pub>Wolters Kluwer Health, Inc</pub><pmid>32706906</pmid><doi>10.1002/hep.31478</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0003-4568-3776</orcidid></addata></record>
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source MEDLINE; Wiley Journals; EZB-FREE-00999 freely available EZB journals
subjects Acute Disease - epidemiology
Acute-On-Chronic Liver Failure
Adult
Aged
Ascites
Bleeding
China - epidemiology
Cirrhosis
Clinical trials
Comorbidity
Consortia
Death
Endoscopy
Esophageal and Gastric Varices - epidemiology
Esophageal and Gastric Varices - mortality
Esophageal and Gastric Varices - surgery
Female
Follow-Up Studies
Gastrointestinal Hemorrhage - epidemiology
Gastrointestinal Hemorrhage - mortality
Gastrointestinal Hemorrhage - surgery
Hepatology
Humans
Liver cirrhosis
Liver Cirrhosis - epidemiology
Liver failure
Male
Middle Aged
Mortality
Nomograms
Portasystemic Shunt, Transjugular Intrahepatic - methods
Prognosis
Prospective Studies
Research Design
Retrospective Studies
Risk Assessment
Treatment Outcome
title Risk Stratification Based on Chronic Liver Failure Consortium Acute Decompensation Score in Patients With Child‐Pugh B Cirrhosis and Acute Variceal Bleeding
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