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Hepatitis C virus-infected kidney waitlist patients: Treat now or treat later?
B A Kiberd1, K Doucette2, A J Vinson1
1Departments of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.
Insights
For hepatitis C virus (HCV) positive patients awaiting kidney transplants, immediate direct-acting antiviral (DAA) therapy offers more life years than delayed treatment. However, transplant accessibility may favor delayed therapy in specific regions or for low-risk patients.
Area of Science:
- Nephrology
- Hepatology
- Transplant Surgery
Background:
- Hepatitis C virus (HCV) positive donor kidneys are increasingly transplanted into HCV positive recipients, reducing wait times.
- Direct-acting antiviral (DAA) therapy offers a high cure rate for HCV, raising questions about optimal treatment timing relative to transplantation.
- Limited organ availability for HCV positive candidates necessitates careful consideration of treatment strategies.
Purpose of the Study:
- To compare the long-term outcomes of immediate versus delayed direct-acting antiviral (DAA) therapy in patients waitlisted for kidney transplantation with hepatitis C virus (HCV) infection.
- To evaluate the impact of organ availability and patient mortality risk on the preferred DAA therapy strategy.
Main Methods:
- A Markov medical decision analysis model was employed to simulate and compare two treatment options for HCV positive waitlisted patients.
- Option 1: Delayed DAA therapy with earlier transplantation. Option 2: Immediate DAA therapy.
- Model outcomes included cumulative transplant incidence and life years gained.
Main Results:
- Immediate DAA therapy (Option 2) resulted in 0.43 more life years gained compared to delayed DAA therapy (Option 1).
- Delayed DAA therapy (Option 1) showed a higher cumulative transplant incidence (54% at 5 years) versus immediate DAA therapy (45% at 5 years).
- Delayed DAA therapy was favored in regions with high HCV positive organ availability or for patients with very low HCV-associated mortality.
Conclusions:
- Immediate DAA therapy generally provides superior long-term survival benefits for HCV positive kidney transplant candidates.
- The optimal strategy depends on individual patient factors, including regional organ availability and HCV-related mortality risk.
- Personalized decision-making is crucial for balancing transplantation access and the benefits of early HCV cure.
Abstract:
Currently many but not all centers transplant hepatitis C virus (HCV) viremic positive (+) donor kidneys into HCV+ recipients. Directed donation of HCV+ organs reduces the wait time to transplantation for HCV+ patients. Direct-acting antiviral (DAA) therapy can cure HCV in virtually all who are infected. Some have suggested that treatment of HCV+ waitlisted patients be deferred with the hope that earlier transplantation will provide better outcomes than early DAA therapy. However, there are not enough organs to guarantee prompt transplantation for the current waitlist of infected candidates. A Markov medical decision analysis model was created to compare the overall outcomes of delayed DAA therapy (Option 1) to immediate DAA therapy (Option 2) in waitlisted HCV+ patients. Option 1 patients were modeled to be transplanted 1 year earlier, with a higher cumulative transplant incidence (54% at 5 years post-listing vs 45% for Option 2). Despite this, Option 2 provided 0.43 (95% confidence interval [CI] 0.38-0.49) more life years than Option 1. However, Option 1 was preferred for regions with much greater access to HCV+ organs or in patients with very low HCV+-associated mortality. The best option from an individual patient's perspective will differ by region and candidate.
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