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Published on: October 11, 2013
Impact of hepatitis C virus and direct acting antivirals on kidney recipients: a retrospective study
Mohamed Gendia1,2, Pietro Lampertico3,4, Carlo Maria Alfieri1
1Unit of Nephrology, Dialysis and Renal Transplant, Department of Medicine, Fondazione Ca' Granda IRCCS Ospedale Maggiore Policlinico di Milano, Milan, Italy.
Insights
Direct acting antivirals (DAAs) effectively treat Hepatitis C virus (HCV) in kidney transplant patients, improving outcomes and showing a high safety profile. Treatment led to sustained virological response without negatively impacting kidney graft function.
Area of Science:
- Nephrology
- Hepatology
- Transplantation Immunology
Background:
- Hepatitis C virus (HCV) infection poses significant risks for kidney transplant recipients, potentially leading to poorer patient and graft outcomes.
- Understanding the impact of HCV and emerging treatments is crucial for managing this patient population.
Purpose of the Study:
- To evaluate the impact of active Hepatitis C virus infection on kidney transplant recipients.
- To assess the safety and efficacy of direct-acting antivirals (DAAs) in treating HCV in kidney transplant patients.
Main Methods:
- Retrospective analysis of 616 kidney transplant recipients.
- Categorization into three groups: DAAs treated (Group A), untreated HCV RNA positive (Group B), and HCV RNA negative (Group C).
- Monitoring of viral load, liver enzymes, proteinuria, and patient/graft survival.
Main Results:
- All DAAs-treated patients achieved HCV RNA negativity, with 92.3% attaining sustained virological response (SVR).
- The untreated HCV RNA positive group experienced significantly higher rates of liver enzyme elevation and death.
- DAA treatment showed a high safety profile, with no significant negative impact on allograft function, particularly in well-functioning grafts.
Conclusions:
- Active HCV infection adversely affects kidney transplant recipients.
- DAAs are safe and effective for treating HCV in kidney transplant patients, leading to high SVR rates and improved outcomes.
- DAA therapy demonstrates a favorable safety profile post-kidney transplant, preserving allograft function.
Abstract:
Hepatitis C virus (HCV) in kidney transplanted patients (KTx-p) carries a high risk for a worse outcome. This retrospective study evaluates the impact of HCV and of the new direct acting antivirals (DAAs) on patient and graft outcomes in KTx patients. Forty (6.5%) of the 616 KTx-p, who received a kidney transplantation (KTx) in our Centre had antibodies against HCV: 13 were positive for HCV RNA and received DAAs (Group A); 11 were HCV RNA positive and did not receive any treatment (Group B; n = 11); 16 were negative for HCV RNA (Group C). All Group A patients had HCV RNA negativity after 12 weeks of treatment, and 12 (92.30%) achieved a sustained virological response (SVR). Only two patients, who had proteinuria greater than 500 mg/day showed a worsening of proteinuria after antiviral therapy in Group A. Liver enzyme elevation and death were significantly more frequent in Group B than other groups. Our results support the notion that active HCV infection negatively affects kidney recipients and that DAA have a high safety and efficacy profile after KTx with no significant negative effect on allograft function, particularly in well-functioning renal grafts.
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