| Literature DB >> 29701909 |
D A Axelrod1, M A Schnitzler2, T Alhamad3, F Gordon1, R D Bloom4, G P Hess5, H Xiao2, M Nazzal2, D L Segev6, V R Dharnidharka3, A S Naik7, N N Lam8, R Ouseph2, B L Kasiske9, C M Durand6, K L Lentine2.
Abstract
Direct-acting antiviral medications (DAAs) have revolutionized care for hepatitis C positive (HCV+) liver (LT) and kidney (KT) transplant recipients. Scientific Registry of Transplant Recipients registry data were integrated with national pharmaceutical claims (2007-2016) to identify HCV treatments before January 2014 (pre-DAA) and after (post-DAA), stratified by donor (D) and recipient (R) serostatus and payer. Pre-DAA, 18% of HCV+ LT recipients were treated within 3 years and without differences by donor serostatus or payer. Post-DAA, only 6% of D-/R+ recipients, 19.8% of D+/R+ recipients with public insurance, and 11.3% with private insurance were treated within 3 years (P < .0001). LT recipients treated for HCV pre-DAA experienced higher rates of graft loss (adjusted hazard ratio [aHR] 1.34 1.852.10 , P < .0001) and death (aHR 1.47 1.681.91 , P < .0001). Post-DAA, HCV treatment was not associated with death (aHR 0.34 0.671.32 , P = .25) or graft failure (aHR 0.32 0.641.26 , P = .20) in D+R+ LT recipients. Treatment increased in D+R+ KT recipients (5.5% pre-DAA vs 12.9% post-DAA), but did not differ by payer status. DAAs reduced the risk of death after D+/R+ KT by 57% (0.19 0.430.95 , P = .04) and graft loss by 46% (0.27 0.541.07 , P = .08). HCV treatment with DAAs appears to improve HCV+ LT and KT outcomes; however, access to these medications appears limited in both LT and KT recipients.Entities:
Keywords: clinical research/practice; economics; health services and outcomes research; infection and infectious agents - viral: hepatitis C; kidney (allograft) function/dysfunction; kidney transplantation/nephrology; liver allograft function/dysfunction; liver transplantation/hepatology; patient survival
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Year: 2018 PMID: 29701909 PMCID: PMC6409105 DOI: 10.1111/ajt.14895
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086