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clinical course and prognostic factors of hepatorenal syndrome:a retrospective single-center cohort study

AIM: To investigate clinical and biochemical features of hepatorenal syndrome(HRS), to assess short and long- term survival evaluating potential predictors of early mortality. METHODS: Sixty-two patients with liver cirrhosis and renal failure, defined as a serum creatinine value > 1.5 mg/dL o...

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Published in:World journal of hepatology 2013-12, Vol.5 (12), p.685-691
Main Authors: Licata, Anna, Maida, Marcello, Bonaccorso, Ambra, Macaluso, Fabio Salvatore, Cappello, Maria, Craxì, Antonio, Almasio, Piero Luigi
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description AIM: To investigate clinical and biochemical features of hepatorenal syndrome(HRS), to assess short and long- term survival evaluating potential predictors of early mortality. METHODS: Sixty-two patients with liver cirrhosis and renal failure, defined as a serum creatinine value > 1.5 mg/dL on at least two measurements within 48 h, admitted to our tertiary referral Unit from 2001 to 201, were retrospectively reviewed. Among them, 33 patients(53.2%) fulfilled the revised criteria of the International Ascites Club for the diagnosis of HRS. Twenty-eight patients were treated with combinations of terlipressin and albumin, two with dopamine and al- bumin, and three with albumin alone. No patients were suitable for liver transplantation. Complete response was defined as normalization of creatinine levels to less than 1.5 mg/dL, partial response as a decrease of at least 50% but not to less than 1.5 mg/dL, no response as no reduction in creatinine or a decrease of less 50% compared to pre-treatment values. All of the patients were followed up for at least 1 year until January 2013. RESULTS: HRS type 1 was diagnosed in 15 patients(45.5%). Hepatitis C virus infection was the primary etiology(69.6%), followed by alcohol(15.2%), and cryptogenesis(15.2%). Complete response to therapy was obtained in only 3 cases(9.1%) and partial re- sponse in 7 patients(21.2%). Median survival was 30 d(range: 10-274) without significant differences be- tween type 1 and type 2 HRS. By univariate analysis, Child-Pugh class C(P = 0.009), presence of hepatocel- lular carcinoma(P = 0.04), low serum sodium(P = 0.02), high bilirubin values(P = 0.009) and high Model for End-stage Liver Disease(MELD) score(P = 0.03) were predictive factors of 30-d mortality. By multivari- ate analysis, only serum sodium < 132 mEq/L(OR = 31.39; P = 0.02) and MELD score > 27(OR = 18.72; P = 0.01) were independently associated with a survival of less than one month. CONCLUSION: HRS still has a poor prognosis, even when vasoactive drug therapies are extensively used.
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METHODS: Sixty-two patients with liver cirrhosis and renal failure, defined as a serum creatinine value &amp;gt; 1.5 mg/dL on at least two measurements within 48 h, admitted to our tertiary referral Unit from 2001 to 201, were retrospectively reviewed. Among them, 33 patients(53.2%) fulfilled the revised criteria of the International Ascites Club for the diagnosis of HRS. Twenty-eight patients were treated with combinations of terlipressin and albumin, two with dopamine and al- bumin, and three with albumin alone. No patients were suitable for liver transplantation. Complete response was defined as normalization of creatinine levels to less than 1.5 mg/dL, partial response as a decrease of at least 50% but not to less than 1.5 mg/dL, no response as no reduction in creatinine or a decrease of less 50% compared to pre-treatment values. All of the patients were followed up for at least 1 year until January 2013. RESULTS: HRS type 1 was diagnosed in 15 patients(45.5%). Hepatitis C virus infection was the primary etiology(69.6%), followed by alcohol(15.2%), and cryptogenesis(15.2%). Complete response to therapy was obtained in only 3 cases(9.1%) and partial re- sponse in 7 patients(21.2%). Median survival was 30 d(range: 10-274) without significant differences be- tween type 1 and type 2 HRS. By univariate analysis, Child-Pugh class C(P = 0.009), presence of hepatocel- lular carcinoma(P = 0.04), low serum sodium(P = 0.02), high bilirubin values(P = 0.009) and high Model for End-stage Liver Disease(MELD) score(P = 0.03) were predictive factors of 30-d mortality. By multivari- ate analysis, only serum sodium &amp;lt; 132 mEq/L(OR = 31.39; P = 0.02) and MELD score &amp;gt; 27(OR = 18.72; P = 0.01) were independently associated with a survival of less than one month. CONCLUSION: HRS still has a poor prognosis, even when vasoactive drug therapies are extensively used.</description><identifier>ISSN: 1948-5182</identifier><identifier>EISSN: 1948-5182</identifier><identifier>DOI: 10.4254/wjh.v5.i12.685</identifier><identifier>PMID: 24432185</identifier><language>eng</language><publisher>United States: Baishideng Publishing Group Co., Limited</publisher><subject>cirrhosis ; drugs ; Hepatitis ; Hepatorenal ; Liver ; Mortality ; Original ; syndrome ; vasoactive ; virus</subject><ispartof>World journal of hepatology, 2013-12, Vol.5 (12), p.685-691</ispartof><rights>2013 Baishideng Publishing Group Co., Limited. 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METHODS: Sixty-two patients with liver cirrhosis and renal failure, defined as a serum creatinine value &amp;gt; 1.5 mg/dL on at least two measurements within 48 h, admitted to our tertiary referral Unit from 2001 to 201, were retrospectively reviewed. Among them, 33 patients(53.2%) fulfilled the revised criteria of the International Ascites Club for the diagnosis of HRS. Twenty-eight patients were treated with combinations of terlipressin and albumin, two with dopamine and al- bumin, and three with albumin alone. No patients were suitable for liver transplantation. Complete response was defined as normalization of creatinine levels to less than 1.5 mg/dL, partial response as a decrease of at least 50% but not to less than 1.5 mg/dL, no response as no reduction in creatinine or a decrease of less 50% compared to pre-treatment values. All of the patients were followed up for at least 1 year until January 2013. RESULTS: HRS type 1 was diagnosed in 15 patients(45.5%). Hepatitis C virus infection was the primary etiology(69.6%), followed by alcohol(15.2%), and cryptogenesis(15.2%). Complete response to therapy was obtained in only 3 cases(9.1%) and partial re- sponse in 7 patients(21.2%). Median survival was 30 d(range: 10-274) without significant differences be- tween type 1 and type 2 HRS. By univariate analysis, Child-Pugh class C(P = 0.009), presence of hepatocel- lular carcinoma(P = 0.04), low serum sodium(P = 0.02), high bilirubin values(P = 0.009) and high Model for End-stage Liver Disease(MELD) score(P = 0.03) were predictive factors of 30-d mortality. By multivari- ate analysis, only serum sodium &amp;lt; 132 mEq/L(OR = 31.39; P = 0.02) and MELD score &amp;gt; 27(OR = 18.72; P = 0.01) were independently associated with a survival of less than one month. CONCLUSION: HRS still has a poor prognosis, even when vasoactive drug therapies are extensively used.</description><subject>cirrhosis</subject><subject>drugs</subject><subject>Hepatitis</subject><subject>Hepatorenal</subject><subject>Liver</subject><subject>Mortality</subject><subject>Original</subject><subject>syndrome</subject><subject>vasoactive</subject><subject>virus</subject><issn>1948-5182</issn><issn>1948-5182</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpVkc9rHCEUx4fS0oQk1xyL0EsvM9VRR-2hUEJ_QSCX5iyuvtkxzOpEnQ3739eQbdh68YFfP-_xPk1zTXDHes4-Pz1M3Z53nvTdIPmb5pwoJltOZP_2pD5rrnJ-wPUwNigp3zdnPWO0J5KfN97OPnhrZmTjmjIgExxaUtyGmIu3aDS2xJRRHNEEi6k1hBrOh-BS3MEXgxKUFPMCtvg9oOzDdobWQiiQKnOKqaBcVne4bN6NZs5wdbwvmvsf3__c_Gpv737-vvl221pGZGkpHy1wy7lhBhwIaaQgwlEQtHcUb3ivxCClchsu-1EOG0XwQPngFBghjKIXzdcX7rJuduCeJ0lm1kvyO5MOOhqv_38JftLbuNdUCjUoXAGfjoAUH1fIRe98tjDPJkBcsyZMYUEw4bJGu5eorSvICcbXNgTrZ0W6KtJ7rqsiXRXVDx9Oh3uN_xNSAx-PxCmG7WPd5gkSU0zJwDH9CyPvnNA</recordid><startdate>20131227</startdate><enddate>20131227</enddate><creator>Licata, Anna</creator><creator>Maida, Marcello</creator><creator>Bonaccorso, Ambra</creator><creator>Macaluso, Fabio Salvatore</creator><creator>Cappello, Maria</creator><creator>Craxì, Antonio</creator><creator>Almasio, Piero Luigi</creator><general>Baishideng Publishing Group Co., Limited</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20131227</creationdate><title>clinical course and prognostic factors of hepatorenal syndrome:a retrospective single-center cohort study</title><author>Licata, Anna ; Maida, Marcello ; Bonaccorso, Ambra ; Macaluso, Fabio Salvatore ; Cappello, Maria ; Craxì, Antonio ; Almasio, Piero Luigi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-35fce5c55a4aede78a8717d3e732d30b52976889db582f86b9106356d9ea77a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>cirrhosis</topic><topic>drugs</topic><topic>Hepatitis</topic><topic>Hepatorenal</topic><topic>Liver</topic><topic>Mortality</topic><topic>Original</topic><topic>syndrome</topic><topic>vasoactive</topic><topic>virus</topic><toplevel>online_resources</toplevel><creatorcontrib>Licata, Anna</creatorcontrib><creatorcontrib>Maida, Marcello</creatorcontrib><creatorcontrib>Bonaccorso, Ambra</creatorcontrib><creatorcontrib>Macaluso, Fabio Salvatore</creatorcontrib><creatorcontrib>Cappello, Maria</creatorcontrib><creatorcontrib>Craxì, Antonio</creatorcontrib><creatorcontrib>Almasio, Piero Luigi</creatorcontrib><collection>维普_期刊</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>维普中文期刊数据库</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Licata, Anna</au><au>Maida, Marcello</au><au>Bonaccorso, Ambra</au><au>Macaluso, Fabio Salvatore</au><au>Cappello, Maria</au><au>Craxì, Antonio</au><au>Almasio, Piero Luigi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>clinical course and prognostic factors of hepatorenal syndrome:a retrospective single-center cohort study</atitle><jtitle>World journal of hepatology</jtitle><addtitle>World Journal of Hepatology</addtitle><date>2013-12-27</date><risdate>2013</risdate><volume>5</volume><issue>12</issue><spage>685</spage><epage>691</epage><pages>685-691</pages><issn>1948-5182</issn><eissn>1948-5182</eissn><abstract>AIM: To investigate clinical and biochemical features of hepatorenal syndrome(HRS), to assess short and long- term survival evaluating potential predictors of early mortality. METHODS: Sixty-two patients with liver cirrhosis and renal failure, defined as a serum creatinine value &amp;gt; 1.5 mg/dL on at least two measurements within 48 h, admitted to our tertiary referral Unit from 2001 to 201, were retrospectively reviewed. Among them, 33 patients(53.2%) fulfilled the revised criteria of the International Ascites Club for the diagnosis of HRS. Twenty-eight patients were treated with combinations of terlipressin and albumin, two with dopamine and al- bumin, and three with albumin alone. No patients were suitable for liver transplantation. Complete response was defined as normalization of creatinine levels to less than 1.5 mg/dL, partial response as a decrease of at least 50% but not to less than 1.5 mg/dL, no response as no reduction in creatinine or a decrease of less 50% compared to pre-treatment values. All of the patients were followed up for at least 1 year until January 2013. RESULTS: HRS type 1 was diagnosed in 15 patients(45.5%). Hepatitis C virus infection was the primary etiology(69.6%), followed by alcohol(15.2%), and cryptogenesis(15.2%). Complete response to therapy was obtained in only 3 cases(9.1%) and partial re- sponse in 7 patients(21.2%). Median survival was 30 d(range: 10-274) without significant differences be- tween type 1 and type 2 HRS. By univariate analysis, Child-Pugh class C(P = 0.009), presence of hepatocel- lular carcinoma(P = 0.04), low serum sodium(P = 0.02), high bilirubin values(P = 0.009) and high Model for End-stage Liver Disease(MELD) score(P = 0.03) were predictive factors of 30-d mortality. By multivari- ate analysis, only serum sodium &amp;lt; 132 mEq/L(OR = 31.39; P = 0.02) and MELD score &amp;gt; 27(OR = 18.72; P = 0.01) were independently associated with a survival of less than one month. 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subjects cirrhosis
drugs
Hepatitis
Hepatorenal
Liver
Mortality
Original
syndrome
vasoactive
virus
title clinical course and prognostic factors of hepatorenal syndrome:a retrospective single-center cohort study
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