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Kidney Transplantation From Hepatitis-C Viraemic Donors:Considerations for Practice in the United Kingdom
Background: Donor hepatitis-C (HCV) infection has historically represented a barrier to kidney transplantation (KT). However, direct-acting antiviral (DAA) medications have revolutionised treatment of chronic HCV infection. Recent American studies have demonstrated that DAA regimes can be used safel...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110637/ https://www.ncbi.nlm.nih.gov/pubmed/35592447 http://dx.doi.org/10.3389/ti.2022.10277 |
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author | Doherty, Daniel T. Athwal, Varinder Moinuddin, Zia Augustine, Titus Prince, Martin van Dellen, David Khambalia, Hussein A. |
author_facet | Doherty, Daniel T. Athwal, Varinder Moinuddin, Zia Augustine, Titus Prince, Martin van Dellen, David Khambalia, Hussein A. |
author_sort | Doherty, Daniel T. |
collection | PubMed |
description | Background: Donor hepatitis-C (HCV) infection has historically represented a barrier to kidney transplantation (KT). However, direct-acting antiviral (DAA) medications have revolutionised treatment of chronic HCV infection. Recent American studies have demonstrated that DAA regimes can be used safely peri-operatively in KT to mitigate HCV transmission risk. Methods: To formulate this narrative review, a comprehensive literature search was performed to analyse results of existing clinical trials examining KT from HCV-positive donors to HCV-negative recipients with peri-operative DAA regimes. Results: 13 studies were reviewed (11 single centre, four retrospective). Outcomes for 315 recipients were available across these studies. A sustained virological response at 12 weeks (SVR12) of 100% was achieved in 11 studies. One study employed an ultra-short DAA regime and achieved an SVR12 of 98%, while another achieved SVR12 of 96% due to treatment of a missed mixed genotype. Conclusion: HCV+ KT is safe and may allow increased utilisation of organs for transplantation from HCV+ donors, who often have other favourable characteristics for successful donation. Findings from US clinical trials can be applied to the United Kingdom transplant framework to improve organ utilisation as suggested by the NHSBT vision strategy “Organ Donation and Transplantation 2030: meeting the need”. |
format | Online Article Text |
id | pubmed-9110637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91106372022-05-18 Kidney Transplantation From Hepatitis-C Viraemic Donors:Considerations for Practice in the United Kingdom Doherty, Daniel T. Athwal, Varinder Moinuddin, Zia Augustine, Titus Prince, Martin van Dellen, David Khambalia, Hussein A. Transpl Int Health Archive Background: Donor hepatitis-C (HCV) infection has historically represented a barrier to kidney transplantation (KT). However, direct-acting antiviral (DAA) medications have revolutionised treatment of chronic HCV infection. Recent American studies have demonstrated that DAA regimes can be used safely peri-operatively in KT to mitigate HCV transmission risk. Methods: To formulate this narrative review, a comprehensive literature search was performed to analyse results of existing clinical trials examining KT from HCV-positive donors to HCV-negative recipients with peri-operative DAA regimes. Results: 13 studies were reviewed (11 single centre, four retrospective). Outcomes for 315 recipients were available across these studies. A sustained virological response at 12 weeks (SVR12) of 100% was achieved in 11 studies. One study employed an ultra-short DAA regime and achieved an SVR12 of 98%, while another achieved SVR12 of 96% due to treatment of a missed mixed genotype. Conclusion: HCV+ KT is safe and may allow increased utilisation of organs for transplantation from HCV+ donors, who often have other favourable characteristics for successful donation. Findings from US clinical trials can be applied to the United Kingdom transplant framework to improve organ utilisation as suggested by the NHSBT vision strategy “Organ Donation and Transplantation 2030: meeting the need”. Frontiers Media S.A. 2022-05-03 /pmc/articles/PMC9110637/ /pubmed/35592447 http://dx.doi.org/10.3389/ti.2022.10277 Text en Copyright © 2022 Doherty, Athwal, Moinuddin, Augustine, Prince, van Dellen and Khambalia. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Health Archive Doherty, Daniel T. Athwal, Varinder Moinuddin, Zia Augustine, Titus Prince, Martin van Dellen, David Khambalia, Hussein A. Kidney Transplantation From Hepatitis-C Viraemic Donors:Considerations for Practice in the United Kingdom |
title | Kidney Transplantation From Hepatitis-C Viraemic Donors:Considerations for Practice in the United Kingdom |
title_full | Kidney Transplantation From Hepatitis-C Viraemic Donors:Considerations for Practice in the United Kingdom |
title_fullStr | Kidney Transplantation From Hepatitis-C Viraemic Donors:Considerations for Practice in the United Kingdom |
title_full_unstemmed | Kidney Transplantation From Hepatitis-C Viraemic Donors:Considerations for Practice in the United Kingdom |
title_short | Kidney Transplantation From Hepatitis-C Viraemic Donors:Considerations for Practice in the United Kingdom |
title_sort | kidney transplantation from hepatitis-c viraemic donors:considerations for practice in the united kingdom |
topic | Health Archive |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110637/ https://www.ncbi.nlm.nih.gov/pubmed/35592447 http://dx.doi.org/10.3389/ti.2022.10277 |
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