Antireflux transoral incisionless fundoplication using EsophyX:: 12-month results of a prospective multicenter study

被引:108
|
作者
Cadiere, Guy-Bernard [1 ]
Buset, Michel [2 ]
Muls, Vinciane [2 ]
Rajan, Amin [3 ]
Roesch, Thomas [4 ]
Eckardt, Alexander J. [4 ]
Weerts, Joseph [5 ]
Bastens, Boris [6 ]
Costamagna, Guido [7 ]
Marchese, Michele [7 ]
Louis, Hubert [8 ]
Mana, Fazia [9 ]
Sermon, Filip [9 ]
Gawlicka, Anna K. [10 ]
Daniel, Michael A. [10 ]
Deviere, Jacques [8 ]
机构
[1] Ctr Hosp Univ St Pierre, Dept Digest Surg, B-1000 Brussels, Belgium
[2] Ctr Hosp Univ St Pierre, Dept Gastroenterol, B-1000 Brussels, Belgium
[3] CHIREC, Clin Parc Leopold, Brussels, Belgium
[4] Charite Univ Med Berlin, Dept Gastroenterol & Hepatol, Berlin, Germany
[5] Ctr Hosp St Joseph, Dept Surg, Liege, Belgium
[6] Ctr Hosp St Joseph, Dept Gastroenterol, Liege, Belgium
[7] Univ Cattolica Sacro Cuore, Digest Endoscopy Unit, Rome, Italy
[8] Univ Libre Bruxelles, Dept Gastroenterol & Hepatopancreatol, Erasme Hosp, Brussels, Belgium
[9] Vrije Univ Brussel, Acad Hosp, Brussels, Belgium
[10] EndoGastr Solut Inc, Redmond, WA USA
关键词
D O I
10.1007/s00268-008-9594-9
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background A novel transoral incisionless fundoplication (TIF) procedure using the EsophyX system with SerosaFuse fasteners was designed to reconstruct a full-thickness valve at the gastroesophageal junction through tailored delivery of multiple fasteners during a single-device insertion. The safety and efficacy of TIF for treating gastroesophageal reflux disease (GERD) were evaluated in a prospective multicenter trial. Methods Patients (n = 86) with chronic GERD treated with proton pump inhibitors (PPIs) were enrolled. Exclusion criteria included an irreducible hiatal hernia > 2 cm. Results The TIF procedure (n = 84) reduced all hiatal hernias (n = 49) and constructed valves measuring 4 cm (2-6 cm) and 230 degrees (160 degrees-300 degrees). Serious adverse events consisted of two esophageal perforations upon device insertion and one case of postoperative intraluminal bleeding. Other adverse events were mild and transient. At 12 months, aggregate (n = 79) and stratified Hill grade I tight (n = 21) results showed 73% and 86% of patients with >= 50% improvement in GERD health-related quality of life (HRQL) scores, 85% discontinuation of daily PPI use, and 81% complete cessation of PPIs; 37% and 48% normalization of esophageal acid exposure; 60% and 89% hiatal hernia reduction; and 62% and 80% esophagitis reduction, respectively. More than 50% of patients with Hill grade I tight valves had a normalized cardia circumference. Resting pressure of the lower esophageal sphincter (LES) was improved significantly (p < 0.001), by 53%. EsophyX-TIF cured GERD in 56% of patients based on their symptom reduction and PPI discontinuation. Conclusions The 12-month results showed that EsophyX-TIF was safe and effective in improving quality of life and for reducing symptoms, PPI use, hiatal hernia, and esophagitis, as well as increasing the LES resting pressure and normalizing esophageal pH and cardia circumference in chronic GERD patients.
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收藏
页码:1676 / 1688
页数:13
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