@article{3967bcce3978415980103c58734abb39,
title = "Intravenous N-Acetylcysteine Improves Transplant-Free Survival in Early Stage Non-Acetaminophen Acute Liver Failure",
abstract = "Background & Aims: N-acetylcysteine (NAC), an antidote for acetaminophen poisoning, might benefit patients with non-acetaminophen-related acute liver failure. Methods: In a prospective, double-blind trial, acute liver failure patients without clinical or historical evidence of acetaminophen overdose were stratified by site and coma grade and assigned randomly to groups that were given NAC or placebo (dextrose) infusion for 72 hours. The primary outcome was overall survival at 3 weeks. Secondary outcomes included transplant-free survival and rate of transplantation. Results: A total of 173 patients received NAC (n = 81) or placebo (n = 92). Overall survival at 3 weeks was 70% for patients given NAC and 66% for patients given placebo (1-sided P = .283). Transplant-free survival was significantly better for NAC patients (40%) than for those given placebo (27%; 1-sided P = .043). The benefits of transplant-free survival were confined to the 114 patients with coma grades I-II who received NAC (52% compared with 30% for placebo; 1-sided P = .010); transplant-free survival for the 59 patients with coma grades III-IV was 9% in those given NAC and 22% in those given placebo (1-sided P = .912). The transplantation rate was lower in the NAC group but was not significantly different between groups (32% vs 45%; P = .093). Intravenous NAC generally was well tolerated; only nausea and vomiting occurred significantly more frequently in the NAC group (14% vs 4%; P = .031). Conclusions: Intravenous NAC improves transplant-free survival in patients with early stage non-acetaminophen-related acute liver failure. Patients with advanced coma grades do not benefit from NAC and typically require emergency liver transplantation.",
author = "Lee, {William M.} and Hynan, {Linda S.} and Lorenzo Rossaro and Fontana, {Robert J.} and Stravitz, {R. Todd} and Larson, {Anne M.} and Davern, {Timothy J.} and Murray, {Natalie G.} and Timothy McCashland and Reisch, {Joan S.} and Robuck, {Patricia R.}",
note = "Funding Information: Funding The study was supported by the following grants: R-03 DK52827, R-01 DK58369, and U-01 DK58369 from the National Institutes of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, and FD-R-001661 from the Orphan Products Division, United States Food and Drug Administration. Additional funding was provided by the Stephen Tips Fund of the Northwestern Medical Foundation and the Jeanne Roberts and Rollin and Mary Ella King Funds of the Southwestern Medical Foundation. This study was performed under IND #56925, filed with the Food and Drug Administration. The N-acetylcysteine used in the trial was supplied initially by Apothecon/Geneva Pharmaceuticals (Princeton, NJ), a division of Bristol Myers Squibb, and after April 2003 was supplied by Cumberland Pharmaceuticals (Nashville, TN). No additional support, data analysis, or input of any kind was provided by these companies. Funding Information: Treatment with NAC may benefit patients with other forms of acute liver failure, 11 either by improving systemic hemodynamics, tissue oxygen delivery, 12–16 or via other favorable effects on the acutely injured liver. 17,18 No clinical trials using NAC for patients with non-acetaminophen acute liver failure have been performed. 19 In 1998, the Acute Liver Failure Study Group, funded by the National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health, began a registry at 24 participating sites around the United States to better characterize and understand mechanisms of acute liver failure. A prospective, randomized, double-blind, placebo-controlled trial of NAC for patients of acute liver failure not caused by acetaminophen was initiated in late 1998, ending in 2006. This article summarizes the outcomes of this trial. ",
year = "2009",
month = sep,
doi = "10.1053/j.gastro.2009.06.006",
language = "English (US)",
volume = "137",
pages = "856--864.e1",
journal = "Gastroenterology",
issn = "0016-5085",
publisher = "W.B. Saunders Ltd",
number = "3",
}