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Direct-Acting Antiviral Therapy and Long-Term Outcomes in Dialysis Patients With Hepatitis C: A Real-world Cohort
Ming-Yan Jiang1,2,3, Jheng-Yan Wu1,4, Yi-Chan Lee5
1Department of Public Health, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Background:
Hepatitis C virus (HCV) infection is associated with adverse outcomes among patients with end-stage kidney disease (ESKD) receiving dialysis. Although direct-acting antivirals (DAAs) achieve high cure rates in patients with ESKD, real-world evidence regarding their long-term clinical benefits remains limited. We evaluated the association between direct-acting antiviral (DAA) therapy and long-term outcomes among dialysis patients with HCV infection.
Method:
We conducted a multicenter retrospective cohort study using the TriNetX research network. Adults (≥18 years) with ESKD receiving dialysis and confirmed HCV infection between 2015 and 2025 were included. Patients were classified as DAA-treated or untreated. The primary outcome was all-cause mortality; secondary outcomes included kidney transplantation, incident cirrhosis, and hepatocellular carcinoma. Propensity score matching (1:1) was performed to balance baseline covariates. Outcomes were analyzed using Cox proportional hazards models with up to 5 years of follow-up.
Results:
Among 7660 patients (1482 DAA-treated and 6178 untreated), 1458 matched pairs were included in the analysis. DAA therapy was associated with lower mortality (HR, 0.68; 95% CI, 0.59-0.77; P < .001) and a higher likelihood of kidney transplantation (hazard ratio [HR], 1.42; 95% confidence interval [CI], 1.12-1.80; P = .004). No significant differences were observed in incident cirrhosis or hepatocellular carcinoma during follow-up. Findings were generally consistent across prespecified subgroups.
Conclusions:
Among patients with ESKD receiving dialysis and HCV infection, DAA therapy was associated with improved long-term survival and a higher likelihood of kidney transplantation. These findings provide real-world evidence supporting the clinical benefits of antiviral therapy and highlight the importance of expanding HCV treatment in dialysis populations.
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