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Real-world Experiences in the Transplantation of Hepatitis C-NAAT–positive Organs
BACKGROUND. Hepatitis C virus (HCV) nucleic acid amplification test (NAAT)–positive donors have increased the organ pool. Direct-acting antivirals (DAAs) have led to high rates of treatment success and sustained virologic response (SVR) in recipients with donor-derived HCV infection without signific...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567032/ https://www.ncbi.nlm.nih.gov/pubmed/37829247 http://dx.doi.org/10.1097/TXD.0000000000001539 |
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author | Steinbrink, Julie M. Byrns, Jennifer Berg, Carl Kappus, Matthew King, Lindsay Ellis, Matthew J. Sanoff, Scott Agarwal, Richa DeVore, Adam D. Reynolds, John M. Hartwig, Matthew G. Milano, Carmelo Sudan, Debra Maziarz, Eileen K. Saullo, Jennifer Alexander, Barbara D. Wolfe, Cameron R. |
author_facet | Steinbrink, Julie M. Byrns, Jennifer Berg, Carl Kappus, Matthew King, Lindsay Ellis, Matthew J. Sanoff, Scott Agarwal, Richa DeVore, Adam D. Reynolds, John M. Hartwig, Matthew G. Milano, Carmelo Sudan, Debra Maziarz, Eileen K. Saullo, Jennifer Alexander, Barbara D. Wolfe, Cameron R. |
author_sort | Steinbrink, Julie M. |
collection | PubMed |
description | BACKGROUND. Hepatitis C virus (HCV) nucleic acid amplification test (NAAT)–positive donors have increased the organ pool. Direct-acting antivirals (DAAs) have led to high rates of treatment success and sustained virologic response (SVR) in recipients with donor-derived HCV infection without significant adverse effects, although variability remains in the timing and duration of antivirals. METHODS. This retrospective study analyzed all adult HCV-NAAT–negative transplant recipients who received an organ from HCV-NAAT–positive donors from November 24, 2018, to March 31, 2022, at Duke University Medical Center with protocolized delay of DAA initiation until after hospital discharge, with at least 180-d follow-up on all patients. Transplant and HCV-related outcomes were analyzed. RESULTS. Two hundred eleven transplants (111 kidneys, 41 livers, 34 hearts, and 25 lungs) were performed from HCV-NAAT–positive donors to HCV-NAAT–negative recipients. Ninety percent of recipients became viremic within 7 d posttransplant. Ninety-nine percent of recipients were initiated on pangenotypic DAAs in the outpatient setting a median of 52 d posttransplant, most commonly with 12-wk courses of sofosbuvir–velpatasvir (lungs) and glecaprevir–pibrentasvir (heart, kidney, and liver). Ninety-seven percent of recipients had SVR after a first-line DAA; all ultimately achieved SVR at 12 wk after subsequent treatment courses. The median peak HCV RNA for all organ systems was 2 436 512 IU/mL; the median time from antiviral to undetectable RNA was 48 d, although differences were noted between organ groups. No patient deaths or graft losses were directly attributable to HCV infection. CONCLUSIONS. One hundred percent of transplant recipients of HCV-NAAT–positive organs ultimately developed SVR without significant adverse effects when HCV antivirals were initiated in the outpatient setting after transplant hospitalization, suggesting that this real-world treatment pathway is a viable option. |
format | Online Article Text |
id | pubmed-10567032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-105670322023-10-12 Real-world Experiences in the Transplantation of Hepatitis C-NAAT–positive Organs Steinbrink, Julie M. Byrns, Jennifer Berg, Carl Kappus, Matthew King, Lindsay Ellis, Matthew J. Sanoff, Scott Agarwal, Richa DeVore, Adam D. Reynolds, John M. Hartwig, Matthew G. Milano, Carmelo Sudan, Debra Maziarz, Eileen K. Saullo, Jennifer Alexander, Barbara D. Wolfe, Cameron R. Transplant Direct Infectious Disease BACKGROUND. Hepatitis C virus (HCV) nucleic acid amplification test (NAAT)–positive donors have increased the organ pool. Direct-acting antivirals (DAAs) have led to high rates of treatment success and sustained virologic response (SVR) in recipients with donor-derived HCV infection without significant adverse effects, although variability remains in the timing and duration of antivirals. METHODS. This retrospective study analyzed all adult HCV-NAAT–negative transplant recipients who received an organ from HCV-NAAT–positive donors from November 24, 2018, to March 31, 2022, at Duke University Medical Center with protocolized delay of DAA initiation until after hospital discharge, with at least 180-d follow-up on all patients. Transplant and HCV-related outcomes were analyzed. RESULTS. Two hundred eleven transplants (111 kidneys, 41 livers, 34 hearts, and 25 lungs) were performed from HCV-NAAT–positive donors to HCV-NAAT–negative recipients. Ninety percent of recipients became viremic within 7 d posttransplant. Ninety-nine percent of recipients were initiated on pangenotypic DAAs in the outpatient setting a median of 52 d posttransplant, most commonly with 12-wk courses of sofosbuvir–velpatasvir (lungs) and glecaprevir–pibrentasvir (heart, kidney, and liver). Ninety-seven percent of recipients had SVR after a first-line DAA; all ultimately achieved SVR at 12 wk after subsequent treatment courses. The median peak HCV RNA for all organ systems was 2 436 512 IU/mL; the median time from antiviral to undetectable RNA was 48 d, although differences were noted between organ groups. No patient deaths or graft losses were directly attributable to HCV infection. CONCLUSIONS. One hundred percent of transplant recipients of HCV-NAAT–positive organs ultimately developed SVR without significant adverse effects when HCV antivirals were initiated in the outpatient setting after transplant hospitalization, suggesting that this real-world treatment pathway is a viable option. Lippincott Williams & Wilkins 2023-10-10 /pmc/articles/PMC10567032/ /pubmed/37829247 http://dx.doi.org/10.1097/TXD.0000000000001539 Text en Copyright © 2023 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Infectious Disease Steinbrink, Julie M. Byrns, Jennifer Berg, Carl Kappus, Matthew King, Lindsay Ellis, Matthew J. Sanoff, Scott Agarwal, Richa DeVore, Adam D. Reynolds, John M. Hartwig, Matthew G. Milano, Carmelo Sudan, Debra Maziarz, Eileen K. Saullo, Jennifer Alexander, Barbara D. Wolfe, Cameron R. Real-world Experiences in the Transplantation of Hepatitis C-NAAT–positive Organs |
title | Real-world Experiences in the Transplantation of Hepatitis C-NAAT–positive Organs |
title_full | Real-world Experiences in the Transplantation of Hepatitis C-NAAT–positive Organs |
title_fullStr | Real-world Experiences in the Transplantation of Hepatitis C-NAAT–positive Organs |
title_full_unstemmed | Real-world Experiences in the Transplantation of Hepatitis C-NAAT–positive Organs |
title_short | Real-world Experiences in the Transplantation of Hepatitis C-NAAT–positive Organs |
title_sort | real-world experiences in the transplantation of hepatitis c-naat–positive organs |
topic | Infectious Disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10567032/ https://www.ncbi.nlm.nih.gov/pubmed/37829247 http://dx.doi.org/10.1097/TXD.0000000000001539 |
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