Abstract

BackgroundHistorically, liver allografts with >30% macrosteatosis (MaS) on donor biopsy have been associated with early allograft dysfunction and worse graft survival; however, successful outcomes have been reported in small cohorts. This study proposes an elevated MaS threshold for organ utilization without detriment to graft survival.MethodsThe UNOS Standard Transplant Analysis and Research database was evaluated for transplants between 2006–2015. Graft survival up to 1-year was evaluated by Kaplan-Meier (KM) survival analyses, and by univariate and multivariable logistic regression analyses, including donor and recipient characteristics. Odds ratios (OR) with 95% confidence intervals (CI) for risk of graft loss are reported.ResultsThirty-day risk of graft loss was increased with MaS as low as 10–19% (OR [95% CI] 1.301 [1.055–1.605], p<0.0001) and peaked with MaS 50–59% (2.921 [1.672–5.103]). At 1-year, risk of graft loss remained elevated with MaS 40–49% (1.465 [1.002–2.142]) and MaS 50–59% (1.978 [1.281–3.056], p = 0.0224). Multivariable models were created for Lower and Higher MELD recipients and MaS cutoffs were established. In Lower MELD recipients, organs with ≥50% MaS had increased risk of graft loss at 30 days (2.451 [1.541–3.897], p = 0.0008) and 1-year post-transplant (1.720 [1.224–2.418], p = 0.0125). Higher MELD recipients had increased risk of graft loss at 30 days with allografts showing MaS ≥40% (4.204 [1.440–5.076], p = 0.0016). At 1-year the risk remained increased, but MaS was not significant predictor of graft loss.048 [1.131–3.710], p = 0.0616). In both MELD cohorts, organs with MaS levels below threshold had similar survival to those transplanted without a donor biopsy.ConclusionsIn conjunction with recipient selection, organs with MaS up to 50% may be safely used without detriment to outcomes.

Highlights

  • Over 13,000 candidates are listed for and awaiting liver transplantation nationwide (UNOS Data as of April 3, 2019)

  • Liver allografts with >30% macrosteatosis (MaS) on donor biopsy have been associated with early allograft dysfunction and worse graft survival; successful outcomes have been reported in small cohorts

  • Thirty-day risk of graft loss was increased with MaS as low as 10–19% (OR [95% confidence intervals (CI)] 1.301 [1.055–1.605], p

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Summary

Introduction

Over 13,000 candidates are listed for and awaiting liver transplantation nationwide (UNOS Data as of April 3, 2019). Hepatic steatosis is common, being reported in 30–51% of donor livers,[3,4] a number that may increase with rising prevalence of obesity and non-alcoholic fatty liver disease in the United States.[5,6] Liver steatosis is characterized as either microvesicular (MiS) or macrovesicular (MaS); only MaS has been shown to significantly influence allograft and patient survival following liver transplantation (LT).[7,8,9,10]The volume of hepatic MaS is based on histologic evaluation and classically described as mild (60%). [15,16,17,18,19,20,21,22,23] These data are derived from small cohorts at single institutions and no large or nationwide studies exist, leaving significant controversy over the utilization of allografts with elevated MaS. This study proposes an elevated MaS threshold for organ utilization without detriment to graft survival

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