In this article, the authors compare NAC infusion during liver procurement with standard portal and aortic flush. A clear allocation paradigm and NAC infusionscheme are described, using dosing and administrationrationale and protocols based on previously published work,5 with the added modihcation of 300mg NAC to initial Celsior flush (Genzyme Corporation, Cambridge, MA).The authors select EAD as their primary endpoint based on the 2013 study by D′Amico et al,5 which notes statistically signihcant differences in liver allograft survival after NAC administration, as well as lower rates of primary dysfunction. In this work, however, no statistically signihcant difference was detected in EAD between groups, even when accounting for different EAD scoring paradigms.Interestingly, supplemental subgroup anal. of livers with prolonged cold ischemia >6 h, which has known association with increased organ injury and post operative complications,6 demonstrates blunting of postoperative transaminase rise, favoring NAC.This suggests a protective effect when a greater degree of ischemic injury is present and mimics prior hndings by D′Amico et al, who reported graft primary dysfunction was lower after NAC treatment in organs with higher baseline donor risk indexes.5 Gomez-Gavara et al also report a trend toward a signihcant decrease in EAD among subjectively steatotic livers treated with NAC. Although intriguing, the results are limited by the small number of patients in these subgroups. Of note is that signihcantly fewer patients in the present study experienced early graft loss requiring transplantation in the NAC group, and no cases of graft loss due to EAD occurred in the NAC treatment group.Although the authors discount the signihcance of this finding due to hepatic artery thrombosis accounting for graft loss in 4 of 7 cases (n = l NAC and n = 3 control), risk of hepatic artery thrombosis is increased in patients with severe ischemia-reperfusion injury due to an increase in intrathepatic resistance to vascular how.7 Further study, especially in extended criteria donors, including a more granular anal. of tissue injury, biomarkers, and clin. outcomes, is necessary to hush out the effect of NAC in grafts at high risk for preservation and reperfusion injury.