The Changing Face of Liver Transplantation in the United States: The Effect of HCV Antiviral Eras on Transplantation Trends and Outcomes

被引:26
作者
Parrish, Nicholas F. [1 ]
Feurer, Irene D. [2 ,3 ,4 ]
Matsuoka, Lea K. [1 ,4 ]
Rega, Scott A. [4 ]
Perri, Roman [4 ,5 ]
Alexopoulos, Sophoclis P. [1 ,4 ]
机构
[1] Vanderbilt Univ, Med Ctr, Sect Surg Sci, Div Hepatobiliary Surg & Liver Transplantat, Nashville, TN USA
[2] Vanderbilt Univ, Med Ctr, Dept Surg, Nashville, TN USA
[3] Vanderbilt Univ, Med Ctr, Dept Biostat, Nashville, TN USA
[4] Vanderbilt Transplant Ctr, Nashville, TN USA
[5] Vanderbilt Univ, Med Ctr, Dept Med, Div Gastroenterol, Nashville, TN USA
来源
TRANSPLANTATION DIRECT | 2019年 / 5卷 / 03期
关键词
NONALCOHOLIC STEATOHEPATITIS; NATURAL-HISTORY; CIRRHOSIS; DISEASE; SURVIVAL; GRAFT; PREVALENCE; PREDICTORS; INFECTION; FAILURE;
D O I
10.1097/TXD.0000000000000866
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background Hepatitis C virus (HCV) cirrhosis is the leading indication for liver transplantation in the United States, although nonalcoholic steatohepatitis (NASH) is on the rise. Increasingly effective HCV antivirals are available, but their association with diagnosis-specific liver transplantation rates and early graft survival is not known. Methods The Scientific Registry of Transplant Recipients database records were retrospectively stratified by HCV antiviral era: interferon (2003-2010), protease inhibitors (2011-2013), and direct-acting antivirals (2014 to present). Kaplan-Meier, chi(2), and multivariable Cox proportional hazards regression models evaluated the effects of antiviral era and etiology of liver disease on transplantation rates and graft survival over 3 years. Results Liver transplants for HCV decreased (35.3% to 23.6%), whereas those for NASH and alcoholic liver disease increased (5.8% to 16.5% and 15.6% to 24.0%) with each advancing era (all P < 0.05). Early graft survival improved with each advancing era for HCV but not for hepatitis B virus, NASH, or alcoholic liver disease (multivariable model era by diagnosis interaction P < 0.001). Era-specific multivariable models demonstrated that the risk of early graft loss for NASH was 22% lower than for HCV in the interferon era (hazard ratio, 0.78; 95% confidence interval, 0.64-0.96; P = 0.02) but risks associated with these diagnoses did not differ significantly in the protease inhibitor (P = 0.06) or direct-acting antiviral eras (P = 0.08). Conclusions Increasing effectiveness of HCV antivirals corresponds with decreased rates of liver transplantation for HCV and improved early graft survival. As the rates of liver transplant for NASH continue to increase, focus will be needed on the prevention and effective therapies for this disease.
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