Management of hepatitis C in patients with chronic kidney disease
Hepatitis C virus(HCV) infection is highly prevalent among chronic kidney disease(CKD) subjects under hemodialysis and in kidney transplantation(KT) recipients, being an important cause of morbidity and mortality in these patients. The vast majority of HCV chronic infections in the hemodialysis sett...
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Veröffentlicht in: | World journal of gastroenterology : WJG 2015-01, Vol.21 (2), p.408-422 |
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description | Hepatitis C virus(HCV) infection is highly prevalent among chronic kidney disease(CKD) subjects under hemodialysis and in kidney transplantation(KT) recipients, being an important cause of morbidity and mortality in these patients. The vast majority of HCV chronic infections in the hemodialysis setting are currently attributable to nosocomial transmission. Acute and chronic hepatitis C exhibits distinct clinical and laboratorial features, which can impact on managementand treatment decisions. In hemodialysis subjects, acute infections are usually asymptomatic and anicteric; since spontaneous viral clearance is very uncommon in this context, acute infections should be treated as soon as possible. In KT recipients, the occurrence of acute hepatitis C can have a more severe course, with a rapid progression of liver fibrosis. In these patients, it is recommended to use pegylated interferon(PEG-IFN) in combination with ribavirin, with doses adjusted according to estimated glomerular filtration rate. There is no evidence suggesting that chronic hepatitis C exhibits a more aggressive course in CKD subjects under conservative management. In these subjects, indication of treatment with PEG-IFN plus ribavirin relies on the CKD stage, rate of progression of renal dysfunction and the possibility of a preemptive transplant. HCV infection has been associated with both liver disease-related deaths and cardiovascular mortality in hemodialysis patients. Among those individuals, low HCV viral loads and the phenomenon of intermittent HCV viremia are often observed, and sequential HCV RNA monitoring is needed. Despite the poor tolerability and suboptimal efficacy of antiviral therapy in CKD patients, many patients can achieve sustained virological response, which improve patient and graft outcomes. Hepatitis C eradication before KT theoretically improves survival and reduces the occurrence of chronic graft nephropathy, de novo glomerulonephritis and post-transplant diabetes mellitus. |
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The vast majority of HCV chronic infections in the hemodialysis setting are currently attributable to nosocomial transmission. Acute and chronic hepatitis C exhibits distinct clinical and laboratorial features, which can impact on managementand treatment decisions. In hemodialysis subjects, acute infections are usually asymptomatic and anicteric; since spontaneous viral clearance is very uncommon in this context, acute infections should be treated as soon as possible. In KT recipients, the occurrence of acute hepatitis C can have a more severe course, with a rapid progression of liver fibrosis. In these patients, it is recommended to use pegylated interferon(PEG-IFN) in combination with ribavirin, with doses adjusted according to estimated glomerular filtration rate. There is no evidence suggesting that chronic hepatitis C exhibits a more aggressive course in CKD subjects under conservative management. In these subjects, indication of treatment with PEG-IFN plus ribavirin relies on the CKD stage, rate of progression of renal dysfunction and the possibility of a preemptive transplant. HCV infection has been associated with both liver disease-related deaths and cardiovascular mortality in hemodialysis patients. Among those individuals, low HCV viral loads and the phenomenon of intermittent HCV viremia are often observed, and sequential HCV RNA monitoring is needed. Despite the poor tolerability and suboptimal efficacy of antiviral therapy in CKD patients, many patients can achieve sustained virological response, which improve patient and graft outcomes. Hepatitis C eradication before KT theoretically improves survival and reduces the occurrence of chronic graft nephropathy, de novo glomerulonephritis and post-transplant diabetes mellitus.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v21.i2.408</identifier><identifier>PMID: 25593456</identifier><language>eng</language><publisher>United States: Baishideng Publishing Group Inc</publisher><subject>Antiviral Agents - adverse effects ; Antiviral Agents - therapeutic use ; Cross Infection - diagnosis ; Cross Infection - drug therapy ; Cross Infection - mortality ; Cross Infection - transmission ; disease;End-stage ; Drug Therapy, Combination ; Hepatitis ; Hepatitis C, Chronic - diagnosis ; Hepatitis C, Chronic - drug therapy ; Hepatitis C, Chronic - mortality ; Hepatitis C, Chronic - transmission ; Humans ; kidney ; Kidney Transplantation - adverse effects ; Kidney Transplantation - mortality ; Renal Dialysis - adverse effects ; Renal Dialysis - mortality ; Renal Insufficiency, Chronic - diagnosis ; Renal Insufficiency, Chronic - mortality ; Renal Insufficiency, Chronic - therapy ; Review ; Risk Factors ; Treatment Outcome ; virus;Chronic</subject><ispartof>World journal of gastroenterology : WJG, 2015-01, Vol.21 (2), p.408-422</ispartof><rights>The Author(s) 2015. 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The vast majority of HCV chronic infections in the hemodialysis setting are currently attributable to nosocomial transmission. Acute and chronic hepatitis C exhibits distinct clinical and laboratorial features, which can impact on managementand treatment decisions. In hemodialysis subjects, acute infections are usually asymptomatic and anicteric; since spontaneous viral clearance is very uncommon in this context, acute infections should be treated as soon as possible. In KT recipients, the occurrence of acute hepatitis C can have a more severe course, with a rapid progression of liver fibrosis. In these patients, it is recommended to use pegylated interferon(PEG-IFN) in combination with ribavirin, with doses adjusted according to estimated glomerular filtration rate. There is no evidence suggesting that chronic hepatitis C exhibits a more aggressive course in CKD subjects under conservative management. In these subjects, indication of treatment with PEG-IFN plus ribavirin relies on the CKD stage, rate of progression of renal dysfunction and the possibility of a preemptive transplant. HCV infection has been associated with both liver disease-related deaths and cardiovascular mortality in hemodialysis patients. Among those individuals, low HCV viral loads and the phenomenon of intermittent HCV viremia are often observed, and sequential HCV RNA monitoring is needed. Despite the poor tolerability and suboptimal efficacy of antiviral therapy in CKD patients, many patients can achieve sustained virological response, which improve patient and graft outcomes. Hepatitis C eradication before KT theoretically improves survival and reduces the occurrence of chronic graft nephropathy, de novo glomerulonephritis and post-transplant diabetes mellitus.</description><subject>Antiviral Agents - adverse effects</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Cross Infection - diagnosis</subject><subject>Cross Infection - drug therapy</subject><subject>Cross Infection - mortality</subject><subject>Cross Infection - transmission</subject><subject>disease;End-stage</subject><subject>Drug Therapy, Combination</subject><subject>Hepatitis</subject><subject>Hepatitis C, Chronic - diagnosis</subject><subject>Hepatitis C, Chronic - drug therapy</subject><subject>Hepatitis C, Chronic - mortality</subject><subject>Hepatitis C, Chronic - transmission</subject><subject>Humans</subject><subject>kidney</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Kidney Transplantation - mortality</subject><subject>Renal Dialysis - adverse effects</subject><subject>Renal Dialysis - mortality</subject><subject>Renal Insufficiency, Chronic - diagnosis</subject><subject>Renal Insufficiency, Chronic - mortality</subject><subject>Renal Insufficiency, Chronic - therapy</subject><subject>Review</subject><subject>Risk Factors</subject><subject>Treatment Outcome</subject><subject>virus;Chronic</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkMFP2zAUh62JCTrGlSPykUuC_Ww39gUJVbAhMe2ynS3HeUkMrVPitIj_Hnd0FfhiP73Pv_f0EXLOWSkqqa9eHrtyC7wMUEqmv5AZADcFaMmOyIwzVhVGQHVCvqX0yBgIoeCYnIBSRkg1n5GbXy66DlcYJzq0tMe1m8IUEl3QEOmuyJ1EX8LUU9-PQwyePoUm4ittQkKX8Dv52rplwrP9fUr-3t3-WfwsHn7_uF_cPBReCjkVde219EwbFB6aqnJcIzQKeauaWlYKEWTdeF8b7Z12yMGxumKtNw5rhnNxSq7fc9ebeoWNz3uNbmnXY1i58dUOLtjPnRh62w1bK8EAVJADLvcB4_C8wTTZVUgel0sXcdgky-cKJAcmeUbLd9SPQ0ojtocxnNmdd5u92-zdBrDZe_5w8XG5A_5fdAbEPrEfYvccYndgDNO7YxSTWholpP730grEG40DkPA</recordid><startdate>20150114</startdate><enddate>20150114</enddate><creator>Carvalho-Filho, Roberto J</creator><creator>Feldner, Ana Cristina C A</creator><creator>Silva, Antonio Eduardo B</creator><creator>Ferraz, Maria Lucia G</creator><general>Baishideng Publishing Group Inc</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</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>5PM</scope></search><sort><creationdate>20150114</creationdate><title>Management of hepatitis C in patients with chronic kidney disease</title><author>Carvalho-Filho, Roberto J ; Feldner, Ana Cristina C A ; Silva, Antonio Eduardo B ; Ferraz, Maria Lucia G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-bbc84c089e3c2d77a18e2d5e1f5db475ee24bdccb98ca8ae12a0b70fc9aeb0e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Antiviral Agents - adverse effects</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Cross Infection - diagnosis</topic><topic>Cross Infection - drug therapy</topic><topic>Cross Infection - mortality</topic><topic>Cross Infection - transmission</topic><topic>disease;End-stage</topic><topic>Drug Therapy, Combination</topic><topic>Hepatitis</topic><topic>Hepatitis C, Chronic - diagnosis</topic><topic>Hepatitis C, Chronic - drug therapy</topic><topic>Hepatitis C, Chronic - mortality</topic><topic>Hepatitis C, Chronic - transmission</topic><topic>Humans</topic><topic>kidney</topic><topic>Kidney Transplantation - adverse effects</topic><topic>Kidney Transplantation - mortality</topic><topic>Renal Dialysis - adverse effects</topic><topic>Renal Dialysis - mortality</topic><topic>Renal Insufficiency, Chronic - diagnosis</topic><topic>Renal Insufficiency, Chronic - mortality</topic><topic>Renal Insufficiency, Chronic - therapy</topic><topic>Review</topic><topic>Risk Factors</topic><topic>Treatment Outcome</topic><topic>virus;Chronic</topic><toplevel>online_resources</toplevel><creatorcontrib>Carvalho-Filho, Roberto J</creatorcontrib><creatorcontrib>Feldner, Ana Cristina C A</creatorcontrib><creatorcontrib>Silva, Antonio Eduardo B</creatorcontrib><creatorcontrib>Ferraz, Maria Lucia G</creatorcontrib><collection>中文科技期刊数据库</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-医药卫生</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>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>Carvalho-Filho, Roberto J</au><au>Feldner, Ana Cristina C A</au><au>Silva, Antonio Eduardo B</au><au>Ferraz, Maria Lucia G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Management of hepatitis C in patients with chronic kidney disease</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World Journal of Gastroenterology</addtitle><date>2015-01-14</date><risdate>2015</risdate><volume>21</volume><issue>2</issue><spage>408</spage><epage>422</epage><pages>408-422</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>Hepatitis C virus(HCV) infection is highly prevalent among chronic kidney disease(CKD) subjects under hemodialysis and in kidney transplantation(KT) recipients, being an important cause of morbidity and mortality in these patients. The vast majority of HCV chronic infections in the hemodialysis setting are currently attributable to nosocomial transmission. Acute and chronic hepatitis C exhibits distinct clinical and laboratorial features, which can impact on managementand treatment decisions. In hemodialysis subjects, acute infections are usually asymptomatic and anicteric; since spontaneous viral clearance is very uncommon in this context, acute infections should be treated as soon as possible. In KT recipients, the occurrence of acute hepatitis C can have a more severe course, with a rapid progression of liver fibrosis. In these patients, it is recommended to use pegylated interferon(PEG-IFN) in combination with ribavirin, with doses adjusted according to estimated glomerular filtration rate. There is no evidence suggesting that chronic hepatitis C exhibits a more aggressive course in CKD subjects under conservative management. In these subjects, indication of treatment with PEG-IFN plus ribavirin relies on the CKD stage, rate of progression of renal dysfunction and the possibility of a preemptive transplant. HCV infection has been associated with both liver disease-related deaths and cardiovascular mortality in hemodialysis patients. Among those individuals, low HCV viral loads and the phenomenon of intermittent HCV viremia are often observed, and sequential HCV RNA monitoring is needed. Despite the poor tolerability and suboptimal efficacy of antiviral therapy in CKD patients, many patients can achieve sustained virological response, which improve patient and graft outcomes. Hepatitis C eradication before KT theoretically improves survival and reduces the occurrence of chronic graft nephropathy, de novo glomerulonephritis and post-transplant diabetes mellitus.</abstract><cop>United States</cop><pub>Baishideng Publishing Group Inc</pub><pmid>25593456</pmid><doi>10.3748/wjg.v21.i2.408</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antiviral Agents - adverse effects Antiviral Agents - therapeutic use Cross Infection - diagnosis Cross Infection - drug therapy Cross Infection - mortality Cross Infection - transmission disease End-stage Drug Therapy, Combination Hepatitis Hepatitis C, Chronic - diagnosis Hepatitis C, Chronic - drug therapy Hepatitis C, Chronic - mortality Hepatitis C, Chronic - transmission Humans kidney Kidney Transplantation - adverse effects Kidney Transplantation - mortality Renal Dialysis - adverse effects Renal Dialysis - mortality Renal Insufficiency, Chronic - diagnosis Renal Insufficiency, Chronic - mortality Renal Insufficiency, Chronic - therapy Review Risk Factors Treatment Outcome virus Chronic |
title | Management of hepatitis C in patients with chronic kidney disease |
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