Endoscopic GERD therapy: a primer for the transoral incisionless fundoplication procedure

被引:14
作者
Bazerbachi, Fateh [1 ]
Krishnan, Kumar [2 ]
Abu Dayyeh, Barham K. [1 ]
机构
[1] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN USA
[2] Massachusetts Gen Hosp, Div Gastroenterol, Boston, MA 02114 USA
关键词
GASTROESOPHAGEAL-REFLUX DISEASE; PROTON-PUMP INHIBITORS; ESOPHYX TIF 2.0; HIATAL-HERNIA; ANTIREFLUX SURGERY; EFFICACY; MULTICENTER; TRIAL; OUTCOMES; ACID;
D O I
10.1016/j.gie.2019.05.028
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Patients with medically refractory GERD have the option of surgery but may opt for effective minimally invasive interventions, when available. However, the primary GERD pharmacologic therapy, proton pump inhibitors, does not satisfactorily address the pathophysiology of the disease. Moreover, a therapeutic gap exists in those severely symptomatic patients who fail medical management and who are poor candidates for surgical fundoplication. Recently, a revival of minimally invasive endoscopic interventions aiming to correct the antireflux barrier has followed existing device modifications, enhancing their safety and efficacy profile. Of these technologies, the transoral incisionless fundoplication (TIF) technique, in its current 2.0 iteration, has been studied in several randomized controlled trials with favorable outcomes and a low rate of adverse events. In this review, we discuss the landscape of endoscopic GERD therapy, focusing on recent updates in the TIF 2.0 procedure with the EsophyX-Z device (EndoGastricSolutions, Redmond, Wash, USA). We discuss the evolution, differences, and improvements in this technique across different generations of the EsophyX device. We also present a framework for candidate selection, based on medical and anatomic considerations. When streamlined within a milieu of comprehensive multidisciplinary programs, these improved endoscopic interventions can provide viable avenues for a carefully selected patients population, bridging therapy gaps, and selectively targeting the primary pathophysiology of the disease.
引用
收藏
页码:370 / 383
页数:14
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