Gastric variceal bleeding is associated with significant morbidity and mortality in patients with portal hypertension and cirrhosis. Options are limited for patients who are not candidates for transjugular intrahepatic portosystemic shunts (TIPS). Cyanoacrylate injections have been reported to be efficacious in previous case series. The aim of this retrospective study was to report our single-center experience with the safety and efficacy of 2-octyl-cyanoacrylate in patients who were not TIPS candidates. Electronic medical records were reviewed for 16 patients who underwent a total of 18 esophagogastroduodenoscopies for acute gastric or duodenal variceal bleeding and secondary prophylaxis of gastric varices; 14 patients had cirrhosis with an average Model for End-Stage Liver Disease score of 16, and 2 patients had noncirrhotic portal hypertension. Primary endpoints of the study included early and delayed rebleeding rate, complications, and death or liver transplantation. The rebleeding rate (early or delayed) was 7%, and no complications were found. One death was reported (unrelated to the procedure). In conclusion, 2-octylcyanoacrylate is a safe and effective alternative for non-TIPS candidates who present with acute gastric variceal bleeding given its low rebleeding and complication rate. I n general, management of acute gastric variceal bleeding consists of a combination of pharmacological therapy (octreotide bolus, followed by infusion), endoscopic therapy (banding ligation in the case of gastroesophageal varices type 1), bridge therapy (balloon tamponade), and rescue therapy (transjugular intrahepatic portosystemic shunts [TIPS]) in cases of high risk of rebleed or refractory bleeding. However, patients with severe decompensation of liver disease or signifi cant thrombus of hepatic vasculature are not ideal candidates for TIPS or balloon-occluded retrograde transvenous obliteration ( 1, 2 ), therefore limiting their therapeutic options to the use of tissue glues. 2-Octyl-cyanoacrylate is a monomer that rapidly polymerizes when it comes into contact with weak bases (blood and water). Several trials have demonstrated a similar hemostasis rate compared with alcohol and ethanolamine, a lower rate of rebleeding compared with band ligation, and a reduced rebleeding rate compared with beta-blockers ( 3-5 ). However, most studies of cyanoacrylate have been performed outside of the United States, mainly in Asia and Europe. Th e purpose of our study was to report our experience with 2-octyl-cyanoacrylate in From the Divisions of Gastroenterology (Lizardo-Sanchez, Burdick) and Hepatology