Literature DB >> 30586641

Use of Hepatitis C Virus Antibody-Positive Donor Livers in Hepatitis C Nonviremic Liver Transplant Recipients.

Keith Luckett1, Tiffany E Kaiser1, Khurram Bari1, Kamran Safdar1, Michael R Schoech1, Senu Apewokin1, Tayyab S Diwan1, Madison C Cuffy1, Nadeem Anwar1, Shimul A Shah2.   

Abstract

BACKGROUND: Given the shortage of available liver grafts, transplantation (LTx) of hepatitis C virus antibody-positive, nucleic acid test-negative (HCV Ab+/NAT-) livers into nonviremic HCV recipients can expand the donor pool. Having previously described the sentinel experience of HCV Ab+/NAT- allografts in nonviremic recipients, we report the growth and extended follow-up of this program for 55 patients compared with recipients of Public Health Services (PHS) increased-risk donor HCV Ab-/NAT- allografts. STUDY
DESIGN: A prospective review of all HCV nonviremic LTx patients receiving HCV Ab+/NAT- organs between March 2016 and August 2018 was performed. All HCV Ab+/NAT- organ recipients underwent HCV testing at 3 months and 1-year post-LTx to determine HCV transmission.
RESULTS: Fifty-five HCV nonviremic candidates received HCV Ab+/NAT- organs; 64% male, median age 59 years (range 36 to 69 years) and median Model for End-Stage Liver Disease score of 22.5. Two recipients were excluded due to death before HCV testing. The HCV disease transmission occurred in 5 recipients (9%). Of these, 4 (80%) underwent anti-HCV treatment with eradication of virus. No patient found to be negative at 3 months seroconverted at 1-year follow-up. No patients who received PHS increased-risk donor HCV Ab-/NAT- organs had viremia develop (0 of 57) and there was no difference in graft and renal function, complications, or survival between HCV Ab+/NAT- recipients and PHS increased-risk donor HCV Ab-/NAT- recipients.
CONCLUSIONS: We report the largest experience with LTx from HCV Ab+/NAT- donors into 55 seronegative recipients with a HCV transmission rate of 9% with no late conversions at 1 year and no difference in function or graft loss compared with PHS increased-risk donor HCV Ab-/NAT- recipients. Due to availability of safe and effective HCV therapies, the use of such organs should be strongly considered to increase the donor organ pool.
Copyright © 2018 American College of Surgeons. Published by Elsevier Inc. All rights reserved.

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Year:  2018        PMID: 30586641     DOI: 10.1016/j.jamcollsurg.2018.12.004

Source DB:  PubMed          Journal:  J Am Coll Surg        ISSN: 1072-7515            Impact factor:   6.113


  4 in total

1.  Center-level trends in utilization of HCV-exposed donors for HCV-uninfected kidney and liver transplant recipients in the United States.

Authors:  Mary G Bowring; Ashton A Shaffer; Allan B Massie; Andrew Cameron; Niraj Desai; Mark Sulkowski; Jacqueline Garonzik-Wang; Dorry L Segev
Journal:  Am J Transplant       Date:  2019-04-09       Impact factor: 8.086

2.  Lower Likelihood of Post-transplant Graft Failure, Death, and Retransplantation in the Era of Direct-Acting Antivirals.

Authors:  Kellie Young; Benny Liu; Taft Bhuket; Robert J Wong
Journal:  J Clin Exp Hepatol       Date:  2020-02-21

Review 3.  Necroptosis in Hepatosteatotic Ischaemia-Reperfusion Injury.

Authors:  Raji Baidya; Darrell H G Crawford; Jérémie Gautheron; Haolu Wang; Kim R Bridle
Journal:  Int J Mol Sci       Date:  2020-08-18       Impact factor: 5.923

4.  Race, Education, and Gender Disparities in Transplantation of Kidneys From Hepatitis C Viremic Donors.

Authors:  Tiffany Nguyen; Meghan E Sise; Cindy Delgado; Winfred Williams; Peter Reese; David Goldberg
Journal:  Transplantation       Date:  2021-08-01       Impact factor: 4.939

  4 in total

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