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Should all dialysis patients with hepatitis C be treated? If so, before or after kidney transplantation?
1Division of Nephrology, Cliniques universitaires Saint-Luc, Université catholique de Louvain, Brussels, Belgium.
Insights
Hepatitis C virus (HCV) infection is now nearly 100% curable in advanced chronic kidney disease (CKD) patients with short, interferon-free regimens. Treatment timing depends on transplant plans and liver fibrosis severity.
Area of Science:
- Hepatology
- Nephrology
- Infectious Diseases
Background:
- Hepatitis C virus (HCV) infection poses significant risks for patients with chronic kidney disease (CKD), particularly those on dialysis.
- Recent advancements offer highly effective, interferon-free treatments for HCV genotypes 1 and 4.
Discussion:
- New 12-week antiviral regimens achieve near 100% cure rates in stage 4-5 CKD patients, including those on dialysis.
- Treatment decisions for HCV in CKD require careful consideration of individual patient factors.
- The optimal timing for initiating HCV antiviral therapy is crucial and depends on several clinical parameters.
Key Insights:
- HCV is now curable in nearly all advanced CKD patients, including dialysis patients, with modern antiviral therapies.
- Interferon-free direct-acting antiviral regimens are effective and well-tolerated, administered over a short 12-week duration.
- Patient management requires a personalized approach, balancing transplant potential, liver fibrosis, and portal hypertension.
Outlook:
- HCV treatment in CKD is expected to become even more streamlined with the upcoming licensing of newer pangenotypic regimens.
- Future strategies may allow for easier treatment of genotypes 2, 3, 5, and 6 after kidney function restoration.
- The high cure rates underscore the importance of treating HCV in CKD patients unless life expectancy is very limited.
Abstract:
HCV infection by genotype 1 and 4 can now be cured in close to 100% of patients with stage 4 or 5 CKD, including dialysis patients. Several regimens are available, all interferon-free and given for only 12 weeks. Thus unless life expectancy is short, HCV infection should be treated. The optimal timing of antiviral treatment will be dependent on several parameters: the possibility of being transplanted rapidly (either with a HCV+ graft or from a living donor) calls for treatment after transplantation. On the contrary, severe liver fibrosis, especially with portal hypertension calls for immediate treatment of HCV. Finally specific HCV genotype also impacts the treatment decision as genotypes 2,3,5 and 6 currently can be treated more easily after restoration of kidney function rather than in the presence of severe CKD, although this is anticipated to change soon once newer pangenotypic regimens are licensed.
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