Patency of endoscopic ultrasound-guided gastroenterostomy in the treatment of malignant gastric outlet obstruction

被引:33
|
作者
Kastelijn, Janine B. [1 ]
Moons, Leon M. G. [1 ]
Garcia-Alonso, Francisco J. [2 ]
Perez-Miranda, Manuel [2 ]
Masaryk, Viliam [3 ]
Will, Uwe [3 ]
Tarantino, Ilaria [4 ]
van Dullemen, Hendrik M. [5 ]
Bijlsma, Rina [6 ]
Poley, Jan-Werner [7 ]
Schwartz, Matthijs P. [8 ]
Vleggaar, Frank P. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Gastroenterol & Hepatol, POB 85500, NL-3508 GA Utrecht, Netherlands
[2] Hosp Univ Rio Hortega, Dept Gastroenterol & Hepatol, Valladolid, Spain
[3] SRH Wald Klinikum, Dept Gastroenterol & Gen Internal Med, Gera, Germany
[4] Mediterranean Inst Transplantat & Adv Specialized, Gastroenterol & Endoscopy Unit, Palermo, Italy
[5] Univ Med Ctr Groningen, Dept Gastroenterol & Hepatol, Groningen, Netherlands
[6] Martini Hosp Groningen, Dept Gastroenterol & Hepatol, Groningen, Netherlands
[7] Erasmus MC, Dept Gastroenterol & Hepatol, Rotterdam, Netherlands
[8] Meander Med Ctr, Dept Gastroenterol & Hepatol, Amersfoort, Netherlands
关键词
APPOSING METAL STENT; LAPAROSCOPIC GASTROJEJUNOSTOMY; SURGICAL GASTROJEJUNOSTOMY; PALLIATION; INTERVENTIONS; MULTICENTER; EXPERIENCE;
D O I
10.1055/a-1214-5659
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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 %), yof 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.
引用
收藏
页码:E1194 / E1201
页数:8
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