Endoscopic ultrasound-guided gastroenterostomy for the management of gastric outlet obstruction: A large comparative study with long-term follow-up

被引:16
|
作者
Jaruvongvanich, Veeravich [1 ]
Mahmoud, Tala [1 ]
Abu Dayyeh, Barham K. [1 ]
Chandrasekhara, Vinay [1 ]
Law, Ryan [1 ]
Storm, Andrew C. [1 ]
Levy, Michael J. [1 ]
Vargas, Eric J. [1 ]
Marya, Neil B. [2 ]
Abboud, Donna M. [1 ]
Ghazi, Rabih [1 ]
Matar, Reem [1 ]
Rapaka, Babusai [1 ]
Buttar, Navtej [1 ]
Truty, Mark J. [3 ]
Aerts, Maridi [4 ]
Messaoudi, Nouredin [5 ]
Kunda, Rastislav [6 ]
机构
[1] Mayo Clin, Div Gastroenterol & Hepatol, 200 First St SW, Rochester, MN 55905 USA
[2] Univ Massachusetts, Med Sch, Div Gastroenterol, Worcester, MA 01605 USA
[3] Mayo Clin, Div Surg, Rochester, MN 55905 USA
[4] Vrije Univ Brussel, Dept Gastroenterol Hepatol, Univ Ziekenhuis Brussel, Brussels, Belgium
[5] Vrije Univ Brussel, Dept Surg, Univ Ziekenhuis Brussel, Brussels, Belgium
[6] Vrije Univ Brussel, Dept Adv Intervent Endoscopy, Univ Ziekenhuis Brussel, Dept Surg,Dept Gastroenterol Hepatol, Brussels, Belgium
关键词
APPOSING METAL STENT; LAPAROSCOPIC GASTROJEJUNOSTOMY; SURGICAL GASTROJEJUNOSTOMY; MULTICENTER;
D O I
10.1055/a-1976-2279
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 Gastric outlet obstruction (GOO) is traditionally managed with surgical gastroenterostomy (surgical-GE) and enteral stenting (ES). Endoscopic ultrasound-guided gastroenterostomy (EUS-GE) is now a third option. Large studies assessing their relative risks and benefits with adequate follow-up are lacking. We conducted a comparative analysis of patients who underwent EUS-GE, ES, or surgical-GE for GOO. Patients and methods In this retrospective comparative cohort study, consecutive patients presenting with GOO who underwent EUS-GE, ES, or surgical-GE at two academic institutions were reviewed and independently cross-edited to ensure accurate reporting. The primary outcome was need for reintervention. Secondary outcomes were technical and clinical success, length of hospital stay (LOS), and adverse events (AEs). Results A total of 436 patients (232 EUS-GE, 131 ES, 73 surgical-GE) were included. The median duration of follow-up of the entire cohort was 185.5 days (interquartile range 55.25-454.25 days). The rate of reintervention in the EUS-GE group was lower than in the ES and surgical-GE groups (0.9 %, 12.2%, and 13.7 %, P < 0.0001). Technical success was achieved in 98.3%, 99.2%, and 100% (P = 0.58), and clinical success was achieved in 98.3%, 91.6%, and 90.4% (P < 0.0001) in the EUS-GE, ES, and surgical-GE groups, respectively. The EUS-GE group had a shorter LOS (2 days vs. 3 days vs. 5 days, P < 0.0001) and a lower AE rate than the ES and surgical-GE groups (8.6% vs. 38.9% vs. 27.4%, P < 0.0001). Conclusion This large cohort study demonstrates the safety and palliation durability of EUS-GE as an alternative strategy for GOO palliation in select patients.
引用
收藏
页码:E60 / E66
页数:7
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