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Diminishing Use of Liver Biopsy among Liver Transplant Recipients for Hepatitis C
Background and Aims: Hepatitis C virus (HCV) cirrhosis is the leading indication for liver transplantation in the United States and recurrent HCV following liver transplantation is a major cause of allograft loss and mortality. Liver biopsies are commonly used to identify recurrent HCV and determine...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
XIA & HE Publishing Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606965/ https://www.ncbi.nlm.nih.gov/pubmed/28936400 http://dx.doi.org/10.14218/JCTH.2016.00073 |
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author | Aby, Elizabeth Jimenez, Melissa A. Grotts, Jonathan F. Agopian, Vatche French, Samuel W. Busuttil, Ronald W. Saab, Sammy |
author_facet | Aby, Elizabeth Jimenez, Melissa A. Grotts, Jonathan F. Agopian, Vatche French, Samuel W. Busuttil, Ronald W. Saab, Sammy |
author_sort | Aby, Elizabeth |
collection | PubMed |
description | Background and Aims: Hepatitis C virus (HCV) cirrhosis is the leading indication for liver transplantation in the United States and recurrent HCV following liver transplantation is a major cause of allograft loss and mortality. Liver biopsies are commonly used to identify recurrent HCV and determine the need for antiviral therapy. The introduction of direct-acting antiviral agents (DAAs) has changed the management of recurrent HCV infection. This study aimed to describe the role of liver biopsies in liver transplant recipients with HCV after the introduction of DAAs. Methods: A retrospective analysis was performed looking at the rate of liver biopsies post-liver transplantation for HCV. The analysis included 475 adult liver transplants for hepatitis C performed at the University of California, Los Angeles from January 1, 2006 to October 1, 2015. Patients were divided into two eras, pre- and post-introduction of DAAs on December 1, 2013. Results: In the era before the introduction of DAAs, the percentage of patients biopsied was significantly higher compared to the era after the introduction of DAAs (56.1% vs. 26.9%, p < 0.001). Conclusions: The introduction of DAAs has changed the management of liver biopsy following liver transplantation and the management of recurrent HCV. Given that DAAs are well tolerated and have high efficacy, liver biopsies are no longer routinely used to justify the use antiviral therapy following liver transplantation. |
format | Online Article Text |
id | pubmed-5606965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | XIA & HE Publishing Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-56069652017-09-21 Diminishing Use of Liver Biopsy among Liver Transplant Recipients for Hepatitis C Aby, Elizabeth Jimenez, Melissa A. Grotts, Jonathan F. Agopian, Vatche French, Samuel W. Busuttil, Ronald W. Saab, Sammy J Clin Transl Hepatol Original Article Background and Aims: Hepatitis C virus (HCV) cirrhosis is the leading indication for liver transplantation in the United States and recurrent HCV following liver transplantation is a major cause of allograft loss and mortality. Liver biopsies are commonly used to identify recurrent HCV and determine the need for antiviral therapy. The introduction of direct-acting antiviral agents (DAAs) has changed the management of recurrent HCV infection. This study aimed to describe the role of liver biopsies in liver transplant recipients with HCV after the introduction of DAAs. Methods: A retrospective analysis was performed looking at the rate of liver biopsies post-liver transplantation for HCV. The analysis included 475 adult liver transplants for hepatitis C performed at the University of California, Los Angeles from January 1, 2006 to October 1, 2015. Patients were divided into two eras, pre- and post-introduction of DAAs on December 1, 2013. Results: In the era before the introduction of DAAs, the percentage of patients biopsied was significantly higher compared to the era after the introduction of DAAs (56.1% vs. 26.9%, p < 0.001). Conclusions: The introduction of DAAs has changed the management of liver biopsy following liver transplantation and the management of recurrent HCV. Given that DAAs are well tolerated and have high efficacy, liver biopsies are no longer routinely used to justify the use antiviral therapy following liver transplantation. XIA & HE Publishing Inc. 2017-05-28 2017-09-28 /pmc/articles/PMC5606965/ /pubmed/28936400 http://dx.doi.org/10.14218/JCTH.2016.00073 Text en © 2017 Authors. http://creativecommons.org/licenses/by-nc/4.0/ This article has been published under the terms of Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0), which permits noncommercial unrestricted use, distribution, and reproduction in any medium, provided that the following statement is provided. “This article has been published in Journal of Clinical and Translational Hepatology at doi:10.14218/JCTH.2016.00073 and can also be viewed on the Journal’s website at http://www.jcthnet.com”. |
spellingShingle | Original Article Aby, Elizabeth Jimenez, Melissa A. Grotts, Jonathan F. Agopian, Vatche French, Samuel W. Busuttil, Ronald W. Saab, Sammy Diminishing Use of Liver Biopsy among Liver Transplant Recipients for Hepatitis C |
title | Diminishing Use of Liver Biopsy among Liver Transplant Recipients for Hepatitis C |
title_full | Diminishing Use of Liver Biopsy among Liver Transplant Recipients for Hepatitis C |
title_fullStr | Diminishing Use of Liver Biopsy among Liver Transplant Recipients for Hepatitis C |
title_full_unstemmed | Diminishing Use of Liver Biopsy among Liver Transplant Recipients for Hepatitis C |
title_short | Diminishing Use of Liver Biopsy among Liver Transplant Recipients for Hepatitis C |
title_sort | diminishing use of liver biopsy among liver transplant recipients for hepatitis c |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5606965/ https://www.ncbi.nlm.nih.gov/pubmed/28936400 http://dx.doi.org/10.14218/JCTH.2016.00073 |
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