Transplantation of kidneys from hepatitis C–infected donors to hepatitis C–negative recipients: Single center experience. Issue 11 (2nd August 2019)
- Record Type:
- Journal Article
- Title:
- Transplantation of kidneys from hepatitis C–infected donors to hepatitis C–negative recipients: Single center experience. Issue 11 (2nd August 2019)
- Main Title:
- Transplantation of kidneys from hepatitis C–infected donors to hepatitis C–negative recipients: Single center experience
- Authors:
- Molnar, Miklos Z.
Nair, Satheesh
Cseprekal, Orsolya
Yazawa, Masahiko
Talwar, Manish
Balaraman, Vasanthi
Podila, Pradeep S. B.
Mas, Valeria
Maluf, Daniel
Helmick, Ryan A.
Campos, Luis
Nezakatgoo, Nosratollah
Eymard, Corey
Horton, Peter
Verma, Rajanshu
Jenkins, Ann Holbrook
Handley, Charlotte R.
Snyder, Heather S.
Cummings, Carolyn
Agbim, Uchenna A.
Maliakkal, Benedict
Satapathy, Sanjaya K.
Eason, James D. - Abstract:
- Abstract : Our aim was to evaluate the safety of transplanting kidneys from HCV‐infected donors in HCV‐uninfected recipients. Data collected from 53 recipients in a single center, observational study included donor and recipient characteristics, liver and kidney graft function, new infections and de novo donor‐specific antibodies and renal histology. Treatment with a direct‐acting antiviral regimen was initiated when HCV RNA was detected. The mean ± SD age of recipients was 53 ± 11 years, 34% were female, 19% and 79% of recipients were white and African American, respectively. The median and interquartile range (IQR) time between transplant and treatment initiation was 76 (IQR: 68‐88) days. All 53 recipients became viremic (genotype: 1a [N = 34], 1b [N = 1], 2 [N = 3], and 3 [N = 15]). The majority (81%) of recipients did not experience clinically significant increases (>3 times higher than upper limit of the normal value) in aminotransferase levels and their HCV RNA levels were in the 5 to 6 log range. One patient developed fibrosing cholestatic hepatitis with complete resolution. All recipients completed antiviral treatment and 100% were HCV RNA–negative and achieved 12‐week sustained virologic response. The estimated GFRs at end of treatment and 12‐week posttreatment were 67 ± 21 mL/min/1.73 m 2 and 67 ± 17 mL/min/1.73 m 2, respectively. Four recipients developed acute rejection. Kidney transplantation from HCV‐infected donors to HCV‐negative recipients should beAbstract : Our aim was to evaluate the safety of transplanting kidneys from HCV‐infected donors in HCV‐uninfected recipients. Data collected from 53 recipients in a single center, observational study included donor and recipient characteristics, liver and kidney graft function, new infections and de novo donor‐specific antibodies and renal histology. Treatment with a direct‐acting antiviral regimen was initiated when HCV RNA was detected. The mean ± SD age of recipients was 53 ± 11 years, 34% were female, 19% and 79% of recipients were white and African American, respectively. The median and interquartile range (IQR) time between transplant and treatment initiation was 76 (IQR: 68‐88) days. All 53 recipients became viremic (genotype: 1a [N = 34], 1b [N = 1], 2 [N = 3], and 3 [N = 15]). The majority (81%) of recipients did not experience clinically significant increases (>3 times higher than upper limit of the normal value) in aminotransferase levels and their HCV RNA levels were in the 5 to 6 log range. One patient developed fibrosing cholestatic hepatitis with complete resolution. All recipients completed antiviral treatment and 100% were HCV RNA–negative and achieved 12‐week sustained virologic response. The estimated GFRs at end of treatment and 12‐week posttreatment were 67 ± 21 mL/min/1.73 m 2 and 67 ± 17 mL/min/1.73 m 2, respectively. Four recipients developed acute rejection. Kidney transplantation from HCV‐infected donors to HCV‐negative recipients should be considered in all eligible patients. Abstract : Transplantation of kidneys from HCV‐infected donors to HCV‐negative recipients, as standard of care, leads to excellent short‐term allograft function and 100% cure rate, but might be associated with relatively high rates of BK, CMV viremia, and consequent development of de novo DSA. Durand et al's editorial is on page 2969 . … (more)
- Is Part Of:
- American journal of transplantation. Volume 19:Issue 11(2019)
- Journal:
- American journal of transplantation
- Issue:
- Volume 19:Issue 11(2019)
- Issue Display:
- Volume 19, Issue 11 (2019)
- Year:
- 2019
- Volume:
- 19
- Issue:
- 11
- Issue Sort Value:
- 2019-0019-0011-0000
- Page Start:
- 3046
- Page End:
- 3057
- Publication Date:
- 2019-08-02
- Subjects:
- clinical research/practice -- hepatitis C -- infection and infectious agents ‐ viral -- kidney (allograft) function/dysfunction -- kidney transplantation/nephrology
Transplantation of organs, tissues, etc -- Periodicals
617.95 - Journal URLs:
- https://www.sciencedirect.com/journal/american-journal-of-transplantation ↗
http://www.blackwellpublishing.com/journal.asp?ref=1600-6135&site=1 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1600-6143 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ajt.15530 ↗
- Languages:
- English
- ISSNs:
- 1600-6135
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0838.850000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 24401.xml