Transoral Incisionless Fundoplication: 2-year Results from the Prospective Multicenter U.S. Study

Author:

Bell Reginald C. W.1,Barnes William E2,Carter Bart J.3,Sewell Robert W.4,Mavrelis Peter G.5,Ihde Glenn M.6,Hoddinott Kevin M.7,Fox Mark A.8,Freeman Katherine D.1,Gunsberger Tanja9,Hausmann Mark G.10,Dargis David11,Gill Brian Dacosta12,Wilson Erik13,Trad Karim S.1415

Affiliation:

1. SurgOne Foregut Institute, Englewood, Colorado;

2. Livingston Hospital and Healthcare Services, Inc. CAH, Salem, Kentucky;

3. Mt. Graham Regional Medical Center, Safford, Arizona;

4. Master Center for Minimally Invasive Surgery, Southlake, Texas;

5. Internal Medicine Associates, Merrillville, Indiana;

6. Ihde Surgical Group, Arlington, Texas;

7. Munroe Regional Medical Center, Ocala, Florida;

8. Crossville Medical Group, PA, Crossville, Tennessee;

9. Tempe St. Luke's Hospital, Tempe, Arizona;

10. The Surgeons Group of Baton Rouge, Baton Rouge, Louisiana;

11. Allegan Surgical Associates, Allegan, Michigan;

12. Utah County Surgical Associates, Provo, Utah;

13. University of Texas Health Science Center, Houston, Texas;

14. The George Washington University School of Medicine and Health Sciences, Washington, DC; and

15. Reston Surgical Associates, Reston, Virginia

Abstract

The aim of this study was to assess prospectively 2-year outcomes of transoral incisionless fundoplication (TIF) in a multicenter setting. A 14-center U.S. registry was designed to evaluate the effects of the TIF 2.0 procedure on chronic gastroesophageal reflux disease (GERD) in over 100 patients. Primary outcome was symptom assessment. Secondary outcomes were proton pump inhibitor (PPI) use, degree of esophagitis, safety, and changes in esophageal acid exposure. One hundred twenty-seven patients underwent TIF between January 2010 and April 2011, 19 (15%) of whom were lost to follow-up. Eight patients undergoing revisional surgery were included, as failures, in the 108 remaining patients. No serious adverse events were reported. GERD Health-related Quality of Life and regurgitation scores improved by 50 per cent or greater in 63 of 96 (66%) and 62 of 88 (70%) patients who had elevated preoperative scores. The Reflux Symptom Index score normalized in 53 of 82 (65%) patients. Daily PPI use decreased from 91 to 29 per cent. In patients amenable to postoperative testing, esophagitis healed in 12 of 16 (75%) and esophageal acid exposure normalized in eight of 14 (57%). TIF safely achieved sustained symptomatic control over a 2-year period in two-thirds of patients with a virtual absence of de novo side effects.

Publisher

SAGE Publications

Subject

General Medicine

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1. Gastroesophageal reflux disease in children: What’s new right now?;World Journal of Gastrointestinal Endoscopy;2023-03-16

2. Transoral incisionless fundoplication for recurrent symptoms after laparoscopic fundoplication;Surgical Endoscopy;2023-01-17

3. Endoluminal Gastroesophageal Reflux Disease Therapies;The SAGES Manual Operating Through the Endoscope;2023

4. Persistent Dysphagia After Prior Anti-Reflux Procedure;The SAGES Manual of Physiologic Evaluation of Foregut Diseases;2023

5. Endoscopic Treatment of Gastroesophageal Reflux Disease;Advances in Surgery;2022-09

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