| Literature DB >> 31306549 |
Miklos Z Molnar1,2,3,4, Satheesh Nair1,2, Orsolya Cseprekal1,2,4, Masahiko Yazawa1,2,5, Manish Talwar1,2, Vasanthi Balaraman1,2, Pradeep S B Podila6,7, Valeria Mas1,2, Daniel Maluf1,2, Ryan A Helmick1,2, Luis Campos1,2, Nosratollah Nezakatgoo1,2, Corey Eymard1,2, Peter Horton1,2, Rajanshu Verma1,2, Ann Holbrook Jenkins1, Charlotte R Handley1, Heather S Snyder1, Carolyn Cummings1, Uchenna A Agbim1,2, Benedict Maliakkal1,2, Sanjaya K Satapathy8, James D Eason1,2.
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 m2 and 67 ± 17 mL/min/1.73 m2 , respectively. Four recipients developed acute rejection. Kidney transplantation from HCV-infected donors to HCV-negative recipients should be considered in all eligible patients.Entities:
Keywords: clinical research/practice; hepatitis C; infection and infectious agents - viral; kidney (allograft) function/dysfunction; kidney transplantation/nephrology
Year: 2019 PMID: 31306549 DOI: 10.1111/ajt.15530
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086