The AXIOSTM (XLUMENA, Inc) stent (ACSEMS), a fully-covered Nitinol stent, has a dual-flange design allowing an anchoring effect to maintain a cystenterostomy tract. Our objective was to evaluate the safety and efficacy of ACSEMS for PP drainage. 7 tertiary care centers (6 US, 1 EU) utilized the following inclusion criteria: symptomatic PP requiring drainage and adherence to

GI lumen that was ≥ 6 cm with ≥ 70% fluid content determined by EUS and/or CT. Technique of cystenterostomy creation and diameter of AXIOSTM stent (10 or 15 mm) was based on endoscopist SCH 900776 research buy preference. Safety outcomes: access site-related bleeding, infection, perforation, tissue injury, and stent migration. Efficacy endpoints: successful Selleckchem Kinase Inhibitor Library insertion and/or removal of ACSEMS, PP resolution defined as ≥ 50% reduction in size, and lumen patency. Follow-up: EUS, and/or CT for PP status at 30 and/or 60 days, and 1 week post-stent removal. From Oct ‘11 to June ‘12, 33 patients (18M; mean age 53 ± 14 yrs) were enrolled with 28 (85%) having underlying chronic pancreatitis. Median PP size was 9.7 ± 4.0 cm. ACSEMS was successfully placed via endoscopic ultrasound

(EUS) guidance in 30/33 (91%) patients, with remaining 3 receiving double pigtail stents. Unsuccessful deployment was due to stent malposition (n=2) and delivery handle malfunction (n=1). Procedure time was 64 ± 38 minutes. PP resolution was achieved in 31/33 (94%); and 28/30 (93%) receiving ACSEMS

with93% lumen patency at stent removal. In ACSEMS subjects, PP size decreased significantly (6.7cm, 95% CI [5.6 - 7.8], p<0.0001) from baseline (10.1 ± 4.0 cm) to 30 days post-stent placement (3.4 ± 3.9 cm). For 10 subjects, the PP size was 1.9 ± 1.6 cm at 60 days. One failure required surgical necrotic debridement and 1 required stent removal post-stent PD184352 (CI-1040) dilation due to debris partially occluding the stent. 11 subjects underwent direct endoscopic necrotic debridement through the indwelling ACSEMS to achieve PP resolution in 9/11 subjects. Complications included abdominal pain (n=3), spontaneous stent migration and back/shoulder pain (n=1), and access-site infection and stent dislodgement (n=1). ACSEMS was successfully placed in 91% of subjects. In ACSEMS subjects, PP resolution of 93% is comparable to plastic pigtail stent data with the distinct advantage of single-step stent deployment and the ability to perform endoscopic necrosectomy through the stent. Optimizing the delivery system and increased operator experience will improve technical success. “
“Subepithelial tumors (SETs) frequently lack distinct EUS features, so final diagnosis demands adequate methods of acquisition of tissue. However, histologic disgnosis of SETs is challenging: EUS-guided FNA is limited by low yield for samller lesions and often fails to provide sufficient tissue for immunohistochemistry (IH).