Literature DB >> 9407343

Hepatitis in patients with end-stage renal disease.

C C Huang1.   

Abstract

Hepatitis B and hepatitis C are two common pathogens causing chronic hepatitis in patients with end-stage renal disease (ESRD). With the acceptance of hepatitis B s antigen (HBsAg) screening, infected patients have been identified and isolated over the past 20 years. Consequently, hepatitis B is now being seen less frequently in dialysis units. Even though hepatitis B has become less of a problem, non-A, non-B hepatitis has been recognized as a significant problem since 1979. With the availability of serological testing for hepatitis C virus (HCV), more specific information is now available in regard to HCV infection in dialysis patients. The prevalence of anti-HCV in haemodialysis (HD) patients is quite variable, ranging from 5 to over 50%. Anti-HCV positivity is associated with previous blood transfusions, mode of therapy and duration of haemodialysis. In Spain and Italy, the annual seroconversion rates of HCV antibodies in dialysis patients are 2-9%; this rate was much higher in Taiwan (15%). Whether patients with HCV infection should be identified and isolated during HD treatment is an issue of controversy. Transplantation is associated with increases in hepatitis B virus (HBV) replicative markers. The survival disadvantage in HBsAg-positive recipients usually did not become apparent until 8 years after transplantation. Hepatitis C virus-infected renal transplant recipients are presumably in a similar situation to patients with hepatitis B, although confirmatory data are currently lacking. Coinfection of HBV and HCV may lead to aggressive liver disease and cirrhosis. A hepatitis B vaccine is recommended for all susceptible dialysis patients. Dialysis patients have lower response rates to hepatitis B vaccines than do other people. Currently, no vaccine is available for hepatitis C. To date, there are no effective treatments available for hepatitis B and hepatitis C. Combination therapy with interferon/lamivudine for hepatitis B and interferon/ribavirin for hepatitis C may offer a promise of effective control of viral replication in the future.

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Year:  1997        PMID: 9407343     DOI: 10.1111/j.1440-1746.1997.tb00506.x

Source DB:  PubMed          Journal:  J Gastroenterol Hepatol        ISSN: 0815-9319            Impact factor:   4.029


  6 in total

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2.  Impaired T cell proliferation, increased soluble death-inducing receptors and activation-induced T cell death in patients undergoing haemodialysis.

Authors:  H J Ankersmit; R Deicher; B Moser; I Teufel; G Roth; S Gerlitz; S Itescu; E Wolner; G Boltz-Nitulescu; J Kovarik
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4.  Efficacy and tolerability of lamivudine in hepatitis B infected renal transplant recipients: A single center study.

Authors:  S K Agarwal; S C Tiwari
Journal:  Indian J Nephrol       Date:  2009-07

5.  Hepatocellular carcinoma in hemodialysis patients.

Authors:  Chern-Horng Lee; Sen-Yung Hsieh; Chih-Chun Chang; I-Kuan Wang; Wen-Hung Huang; Cheng-Hao Weng; Ching-Wei Hsu; Tzung-Hai Yen
Journal:  Oncotarget       Date:  2017-04-16

6.  The relationship between human leukocyte antigen-DP/DQ gene polymorphisms and the outcomes of HCV infection in a Chinese population.

Authors:  Peng Huang; Haozhi Fan; Ting Tian; Peiwen Liao; Jun Li; Rongbin Yu; Xueshan Xia; Yue Feng; Jie Wang; Yuan Liu; Yun Zhang; Ming Yue
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  6 in total

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