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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.
Afiliación
  • Doherty DT; Department of Renal and Pancreatic Transplantation, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
  • Athwal V; Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
  • Moinuddin Z; Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
  • Augustine T; Department of Hepatology, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
  • Prince M; Department of Renal and Pancreatic Transplantation, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
  • van Dellen D; Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.
  • Khambalia HA; Department of Renal and Pancreatic Transplantation, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
Transpl Int ; 35: 10277, 2022.
Article en En | MEDLINE | ID: mdl-35592447
ABSTRACT

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".
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trasplante de Riñón / Hepatitis C / Hepatitis C Crónica Tipo de estudio: Observational_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Transpl Int Asunto de la revista: TRANSPLANTE Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trasplante de Riñón / Hepatitis C / Hepatitis C Crónica Tipo de estudio: Observational_studies Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Transpl Int Asunto de la revista: TRANSPLANTE Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido