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Updated: May 29, 2026

Heterotopic Renal Autotransplantation in a Porcine Model: A Step-by-Step Protocol
Published on: February 21, 2016
Should we be using kidneys from hepatitis C virus-infected donors?
Beatriz Domínguez-Gil1, Amado Andrés, Jose M Campistol
1Organización Nacional de Trasplantes, C/ Sinesio Delgado, Carretera de Andalucía, Madrid, Spain.
Insights
Transplanting kidneys from hepatitis C virus-positive donors (HCVD positive) to HCV-positive recipients offers better survival than remaining on the waitlist. This approach is safe long-term, especially when matching donor and recipient HCV genotypes.
Area of Science:
- Nephrology
- Transplantation Immunology
- Infectious Diseases
Background:
- Kidney transplantation is a vital treatment for end-stage renal disease.
- The use of organs from donors positive for hepatitis C virus (HCV) remains a complex ethical and clinical consideration.
- Decreasing HCV prevalence in dialysis patients leads to underutilization of HCVD-positive donor kidneys.
Purpose of the Study:
- To evaluate the safety and efficacy of transplanting kidneys from HCVD-positive donors into HCV-positive recipients.
- To compare outcomes of recipients of HCVD-positive kidneys with those on the waitlist.
- To explore strategies for improving the utilization of HCVD-positive donor organs.
Main Methods:
- Analysis of registry data comparing outcomes based on donor HCV status.
- Review of collaborative studies on HCV RNA-positive recipients of HCVD-positive kidneys.
- Examination of factors influencing graft and patient survival, including HCV genotype matching.
Main Results:
- Transplantation with HCVD-positive kidneys shortens wait times but may slightly increase risks of death and graft loss compared to HCVD-negative donors.
- Recipients of HCVD-positive kidneys demonstrate improved survival rates compared to patients remaining on the waitlist.
- HCV serology is not an independent long-term risk factor for liver disease, graft survival, or patient survival in this cohort.
- Matching donor and recipient HCV genotypes can enhance the safety of this transplantation strategy.
Conclusions:
- Transplanting kidneys from HCVD-positive donors to HCV-positive recipients is a safe and effective long-term strategy.
- This approach offers superior patient survival compared to remaining on the HCV-positive waitlist.
- Optimizing organ utilization through measures like preemptive transplantation is recommended for surplus HCVD-positive kidneys.
Purpose Of Review:
Transplantation of kidneys from donors with a positive serology for hepatitis C virus (HCVD positive) remains controversial.
Recent Findings:
Registry studies reported that the use of HCVD positive kidneys into HCV positive recipients is associated with shorter time awaiting transplantation but with a small increase in hazard for death and graft loss compared with HCVD negative. Notably, patients who received kidneys from HCVD positive have better survival than those who remain in the waitlist. A collaborative study using HCVD positive kidneys into HCVRNA positive recipients showed that HCV serology was not an independent risk factor for liver disease, graft survival, and patient survival in the long term. The safety of this approach can be improved by matching donors and recipients according to HCV genotypes. Because the incidence and prevalence of HCV infection in dialysis patients are decreasing, kidneys from HCVD positive are becoming surplus organs due to the lack of appropriate recipients in the waitlist. To improve the underutilization of these kidneys, organizational measures, including the offer of these kidneys for preemptive transplantation, are suggested.
Summary:
The use of kidneys from HCVD positive into HCVR positive seems to be a safe approach in the long term, showing a better patient survival than that of HCV positive patients on the waitlist.
Related Concept Videos
Kidney Transplant I: Introduction
Kidney Transplant II: Surgical Procedure
Hepatitis
Kidney Transplant III: Nursing Management
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow

