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Curing Hepatitis C in Liver Transplant Recipients Is Associated with Changes in Immunosuppressant Use

Background and Aims: All-oral interferon-free antivirals are highly effective in treating recurrent hepatitis C (HCV) infection in liver transplant (LT) recipients. The aim of the study was to assess immunosuppression needs after achieving a sustained viral response (SVR). Methods: We compared immun...

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Autores principales: Saab, Sammy, Rheem, Justin, Jimenez, Melissa, Bau, Sherona, Choi, Gina, Durazo, Francisco, El Kabany, Mohammed, Han, Steven, Farid, Alexander, Jamal, Naadir, Grotts, Jonathan, Elashoff, David, Busuttil, Ronald W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: XIA & HE Publishing Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807141/
https://www.ncbi.nlm.nih.gov/pubmed/27047770
http://dx.doi.org/10.14218/JCTH.2016.00001
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author Saab, Sammy
Rheem, Justin
Jimenez, Melissa
Bau, Sherona
Choi, Gina
Durazo, Francisco
El Kabany, Mohammed
Han, Steven
Farid, Alexander
Jamal, Naadir
Grotts, Jonathan
Elashoff, David
Busuttil, Ronald W.
author_facet Saab, Sammy
Rheem, Justin
Jimenez, Melissa
Bau, Sherona
Choi, Gina
Durazo, Francisco
El Kabany, Mohammed
Han, Steven
Farid, Alexander
Jamal, Naadir
Grotts, Jonathan
Elashoff, David
Busuttil, Ronald W.
author_sort Saab, Sammy
collection PubMed
description Background and Aims: All-oral interferon-free antivirals are highly effective in treating recurrent hepatitis C (HCV) infection in liver transplant (LT) recipients. The aim of the study was to assess immunosuppression needs after achieving a sustained viral response (SVR). Methods: We compared immunosuppression needs before and after achieving a SVR in adult LT recipients treated for recurrent HCV infection with all-oral direct acting agents. Results: We identified 52 liver LT treated recipients who achieved a SVR. The median (25th and 75th percentile interquartile range [IQR]) age was 62 years (57.75, 65). Most recipients received tacrolimus (TAC) for their immunosuppressant regimen. After achieving SVR, there was no statistically significant difference in daily dose of TAC unadjusted per weight (p > 0.05). However, there was a statistically significant decrease in daily dose of TAC adjusted per weight, serum levels of TAC, and the product of glomerular filtration rate and TAC. No statistically significant differences in cyclosporine unadjusted/adjusted per weight daily dose or serum levels were noted. Conclusions: Immunosuppression needs were increased for those patients treated with TAC but not cyclosporine. LT recipients prescribed TAC require close monitoring after treatment completion to avoid potential risk of acute rejection.
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spelling pubmed-48071412016-04-04 Curing Hepatitis C in Liver Transplant Recipients Is Associated with Changes in Immunosuppressant Use Saab, Sammy Rheem, Justin Jimenez, Melissa Bau, Sherona Choi, Gina Durazo, Francisco El Kabany, Mohammed Han, Steven Farid, Alexander Jamal, Naadir Grotts, Jonathan Elashoff, David Busuttil, Ronald W. J Clin Transl Hepatol Original Article Background and Aims: All-oral interferon-free antivirals are highly effective in treating recurrent hepatitis C (HCV) infection in liver transplant (LT) recipients. The aim of the study was to assess immunosuppression needs after achieving a sustained viral response (SVR). Methods: We compared immunosuppression needs before and after achieving a SVR in adult LT recipients treated for recurrent HCV infection with all-oral direct acting agents. Results: We identified 52 liver LT treated recipients who achieved a SVR. The median (25th and 75th percentile interquartile range [IQR]) age was 62 years (57.75, 65). Most recipients received tacrolimus (TAC) for their immunosuppressant regimen. After achieving SVR, there was no statistically significant difference in daily dose of TAC unadjusted per weight (p > 0.05). However, there was a statistically significant decrease in daily dose of TAC adjusted per weight, serum levels of TAC, and the product of glomerular filtration rate and TAC. No statistically significant differences in cyclosporine unadjusted/adjusted per weight daily dose or serum levels were noted. Conclusions: Immunosuppression needs were increased for those patients treated with TAC but not cyclosporine. LT recipients prescribed TAC require close monitoring after treatment completion to avoid potential risk of acute rejection. XIA & HE Publishing Inc. 2016-03-15 2016-03-28 /pmc/articles/PMC4807141/ /pubmed/27047770 http://dx.doi.org/10.14218/JCTH.2016.00001 Text en © 2016 The Second Affiliated Hospital of Chongqing Medical University. Published by XIA & HE Publishing Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 4.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Saab, Sammy
Rheem, Justin
Jimenez, Melissa
Bau, Sherona
Choi, Gina
Durazo, Francisco
El Kabany, Mohammed
Han, Steven
Farid, Alexander
Jamal, Naadir
Grotts, Jonathan
Elashoff, David
Busuttil, Ronald W.
Curing Hepatitis C in Liver Transplant Recipients Is Associated with Changes in Immunosuppressant Use
title Curing Hepatitis C in Liver Transplant Recipients Is Associated with Changes in Immunosuppressant Use
title_full Curing Hepatitis C in Liver Transplant Recipients Is Associated with Changes in Immunosuppressant Use
title_fullStr Curing Hepatitis C in Liver Transplant Recipients Is Associated with Changes in Immunosuppressant Use
title_full_unstemmed Curing Hepatitis C in Liver Transplant Recipients Is Associated with Changes in Immunosuppressant Use
title_short Curing Hepatitis C in Liver Transplant Recipients Is Associated with Changes in Immunosuppressant Use
title_sort curing hepatitis c in liver transplant recipients is associated with changes in immunosuppressant use
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807141/
https://www.ncbi.nlm.nih.gov/pubmed/27047770
http://dx.doi.org/10.14218/JCTH.2016.00001
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