| Literature DB >> 25091274 |
S Baid-Agrawal1, M Pascual, D Moradpour, R Somasundaram, M Muche.
Abstract
Chronic hepatitis C virus (HCV) infection remains an important health problem, which is associated with deleterious consequences in kidney transplant recipients. Besides hepatic complications, several extrahepatic complications contribute to reduced patient and allograft survival in HCV-infected kidney recipients. However, HCV infection should not be considered as a contraindication for kidney transplantation because patient survival is better with transplantation than on dialysis. Treatment of HCV infection is currently interferon-alpha (IFN-α) based, which has been associated with higher renal allograft rejection rates. Therefore, antiviral treatment before transplantation is preferable. As in the nontransplant setting, IFN-free treatment regimens, because of their greater efficacy and reduced toxicity, currently represent promising and attractive therapeutic options after kidney transplantation as well. However, clinical trials will be required to closely evaluate these regimens in kidney recipients. There is also a need for prospective controlled studies to determine the optimal immunosuppressive regimens after transplantation in HCV-infected recipients. Combined kidney and liver transplantation is required in patients with advanced liver cirrhosis. However, in patients with cleared HCV infection and early cirrhosis without portal hypertension, kidney transplantation alone may be considered. There is some agreement about the use of HCV-positive donors in HCV-infected recipients, although data regarding posttransplant survival rates are controversial. © Copyright 2014 The American Society of Transplantation and the American Society of Transplant Surgeons.Entities:
Keywords: Clinical research/practice; complication: infectious; complication: medical/metabolic; graft survival; infection and infectious agents; infectious disease; kidney transplantation/nephrology; patient survival; viral: hepatitis C
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Year: 2014 PMID: 25091274 DOI: 10.1111/ajt.12835
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086