Mid-Term Follow-Up of Pancreatic Cysts That Successfully Resolve Following Endoscopic Ultrasound-Guided Ethanol Ablation

2009 ◽  
Vol 69 (5) ◽  
pp. AB323 ◽  
Author(s):  
John M. Dewitt ◽  
Christopher J. Dimaio ◽  
William R. Brugge
2015 ◽  
Vol 34 (3) ◽  
pp. 193-199 ◽  
Author(s):  
Manasa Kandula ◽  
Harsha Moole ◽  
Michael Cashman ◽  
Fritz H. Volmar ◽  
Matthew L. Bechtold ◽  
...  

2015 ◽  
Vol 148 (4) ◽  
pp. S-520-S-521
Author(s):  
Manasa Kandula ◽  
Harsha Moole ◽  
Michael D. Cashman ◽  
Fritz-Henry Volmar ◽  
Matthew L. Bechtold ◽  
...  

2017 ◽  
Vol 42 (4) ◽  
pp. 310-311 ◽  
Author(s):  
Yaping Luo ◽  
Ji Li ◽  
Aiming Yang ◽  
Hongbo Yang ◽  
Fang Li

2018 ◽  
Vol 46 (5) ◽  
pp. 395-399 ◽  
Author(s):  
Ivan Chebib ◽  
Emily Albanese ◽  
Aristana Scourtas ◽  
Martha B. Pitman

Endoscopy ◽  
2020 ◽  
Author(s):  
Dongwook Oh ◽  
Sung Woo Ko ◽  
Dong-Wan Seo ◽  
Seung-Mo Hong ◽  
Jin Hee Kim ◽  
...  

Abstract Background Endoscopic ultrasound-guided radiofrequency ablation (EUS-RFA) has been increasingly used for the management of various solid pancreatic tumors. This study aimed to evaluate the feasibility and safety of EUS-RFA for serous cystic neoplasms (SCNs). Methods 13 patients with microcystic SCNs with honeycomb appearance underwent EUS-RFA using a 19-gauge RFA needle. Before ablation, cystic fluid was aspirated until a thin layer of fluid remained. Results EUS-RFA was successful in all patients. Seven patients underwent a single session and the remaining six patients underwent a second session of EUS-RFA. One patient (7.7 %) experienced self-limited abdominal pain after EUS-RFA. During a median follow-up period of 9.21 months (interquartile range [IQR] 5.93 – 15.38), the median volume of the SCNs decreased from 37.82 mL (IQR 15.03 – 59.53) at baseline to 10.95 mL (IQR 4.79 – 32.39) at the end of follow-up. A radiologic partial response was achieved in eight patients (61.5 %). Conclusions EUS-RFA is technically feasible and showed an acceptable rate of adverse events for patients with SCNs. A long-term follow-up study is required to evaluate the efficacy of EUS-RFA.


2020 ◽  
Vol 08 (09) ◽  
pp. E1194-E1201 ◽  
Author(s):  
Janine B. Kastelijn ◽  
Leon M.G. Moons ◽  
Francisco J. Garcia-Alonso ◽  
Manuel Pérez-Miranda ◽  
Viliam Masaryk ◽  
...  

Abstract Background and study aims Endoscopic ultrasound-guided gastroenterostomy (EUS-GE) with a lumen-apposing metal stent (LAMS) is a novel, minimally invasive technique in the palliative treatment of malignant gastric outlet obstruction (GOO). Several studies have demonstrated feasibility and safety of EUS-GE, but evidence on long-term durability is limited. The aim of this study was to evaluate patency of EUS-GE in treatment of malignant GOO. Patients and Methods An international multicenter study was performed in seven centers in four European countries. Patients who underwent EUS-GE with a LAMS between March 2015 and March 2019 for palliative treatment of symptomatic malignant GOO were included retrospectively. Our main outcome was recurrent obstruction due to LAMS dysfunction; other outcomes of interest were technical success, clinical success, adverse events (AEs), and survival. Results A total of 45 patients (mean age 69.9 ± 12.3 years and 48.9 % male) were included. Median duration of follow-up was 59 days (interquartile range [IQR] 41–128). Recurrent obstruction occurred in two patients (6.1 %), after 33 and 283 days of follow-up. Technical success was achieved in 39 patients (86.7 %). Clinical success was achieved in 33 patients (73.3 %). AEs occurred in 12 patients (26.7 %), of which five were fatal. Median overall survival was 57 days (IQR 32–114). Conclusions EUS-GE showed a low rate of recurrent obstruction. The relatively high number of fatal AEs underscores the importance of careful implementation of EUS-GE in clinical practice.


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