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Transplantation of Renal Allografts From Organ Donors Reactive for HCV Antibodies to HCV-Negative Recipients: Safety and Clinical Outcome
INTRODUCTION: Because of the shortage of available organs for renal transplantation, strategies enabling the safe use of organs from donors with potential chronic infections such as hepatitis C are necessary. The aim of this study was to analyze the outcome of renal transplant donation from hepatiti...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678640/ https://www.ncbi.nlm.nih.gov/pubmed/29142940 http://dx.doi.org/10.1016/j.ekir.2016.09.058 |
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author | Nowak, Knut Michael Witzke, Oliver Sotiropoulos, Georgios C. Benkö, Tamas Fiedler, Melanie Timm, Jörg Kribben, Andreas Wilde, Benjamin Saner, Fuat Paul, Andreas Treckmann, Jürgen |
author_facet | Nowak, Knut Michael Witzke, Oliver Sotiropoulos, Georgios C. Benkö, Tamas Fiedler, Melanie Timm, Jörg Kribben, Andreas Wilde, Benjamin Saner, Fuat Paul, Andreas Treckmann, Jürgen |
author_sort | Nowak, Knut Michael |
collection | PubMed |
description | INTRODUCTION: Because of the shortage of available organs for renal transplantation, strategies enabling the safe use of organs from donors with potential chronic infections such as hepatitis C are necessary. The aim of this study was to analyze the outcome of renal transplant donation from hepatitis C virus (HCV)-positive donors. METHODS: Between September 2002 and May 2007, 51 kidneys (34 donors) reactive for HCV antibodies were further evaluated. Six kidneys (5 donors) were transplanted to 6 recipients with known chronic HCV infection. The remaining 29 donors underwent extended virological testing. Nine donors were HCV RNA positive and thus not suitable for HCV-negative patients. Twenty donors (21 kidneys) did not have detectable HCV RNA copies and were transplanted into 21 HCV-negative recipients. Clinical outcomes focusing on safety, allograft function, and de novo HCV infection in the recipient were collected. RESULTS: There were no de novo HCV infections detected in recipients who were HCV negative before transplantation. The extended virological donor screening did not have an impact on median cold ischemia time. Five-year graft survival was 75%. DISCUSSION: Organs from anti-HCV-reactive, nonviremic donors can be transplanted safely to HCV-negative recipients. |
format | Online Article Text |
id | pubmed-5678640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-56786402017-11-15 Transplantation of Renal Allografts From Organ Donors Reactive for HCV Antibodies to HCV-Negative Recipients: Safety and Clinical Outcome Nowak, Knut Michael Witzke, Oliver Sotiropoulos, Georgios C. Benkö, Tamas Fiedler, Melanie Timm, Jörg Kribben, Andreas Wilde, Benjamin Saner, Fuat Paul, Andreas Treckmann, Jürgen Kidney Int Rep Clinical Research INTRODUCTION: Because of the shortage of available organs for renal transplantation, strategies enabling the safe use of organs from donors with potential chronic infections such as hepatitis C are necessary. The aim of this study was to analyze the outcome of renal transplant donation from hepatitis C virus (HCV)-positive donors. METHODS: Between September 2002 and May 2007, 51 kidneys (34 donors) reactive for HCV antibodies were further evaluated. Six kidneys (5 donors) were transplanted to 6 recipients with known chronic HCV infection. The remaining 29 donors underwent extended virological testing. Nine donors were HCV RNA positive and thus not suitable for HCV-negative patients. Twenty donors (21 kidneys) did not have detectable HCV RNA copies and were transplanted into 21 HCV-negative recipients. Clinical outcomes focusing on safety, allograft function, and de novo HCV infection in the recipient were collected. RESULTS: There were no de novo HCV infections detected in recipients who were HCV negative before transplantation. The extended virological donor screening did not have an impact on median cold ischemia time. Five-year graft survival was 75%. DISCUSSION: Organs from anti-HCV-reactive, nonviremic donors can be transplanted safely to HCV-negative recipients. Elsevier 2016-10-06 /pmc/articles/PMC5678640/ /pubmed/29142940 http://dx.doi.org/10.1016/j.ekir.2016.09.058 Text en © 2016 International Society of Nephrology. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Clinical Research Nowak, Knut Michael Witzke, Oliver Sotiropoulos, Georgios C. Benkö, Tamas Fiedler, Melanie Timm, Jörg Kribben, Andreas Wilde, Benjamin Saner, Fuat Paul, Andreas Treckmann, Jürgen Transplantation of Renal Allografts From Organ Donors Reactive for HCV Antibodies to HCV-Negative Recipients: Safety and Clinical Outcome |
title | Transplantation of Renal Allografts From Organ Donors Reactive for HCV Antibodies to HCV-Negative Recipients: Safety and Clinical Outcome |
title_full | Transplantation of Renal Allografts From Organ Donors Reactive for HCV Antibodies to HCV-Negative Recipients: Safety and Clinical Outcome |
title_fullStr | Transplantation of Renal Allografts From Organ Donors Reactive for HCV Antibodies to HCV-Negative Recipients: Safety and Clinical Outcome |
title_full_unstemmed | Transplantation of Renal Allografts From Organ Donors Reactive for HCV Antibodies to HCV-Negative Recipients: Safety and Clinical Outcome |
title_short | Transplantation of Renal Allografts From Organ Donors Reactive for HCV Antibodies to HCV-Negative Recipients: Safety and Clinical Outcome |
title_sort | transplantation of renal allografts from organ donors reactive for hcv antibodies to hcv-negative recipients: safety and clinical outcome |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678640/ https://www.ncbi.nlm.nih.gov/pubmed/29142940 http://dx.doi.org/10.1016/j.ekir.2016.09.058 |
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