Abstract

Introduction: Outcomes of laparoscopic procedures for gastroesophageal reflux disease (GERD) are variable depending on surgical expertise and/or patient-related factors. Some procedures may be inadequate in patients with severe disease. Effectiveness of laparoscopic magnetic sphincter augmentation (MSA) has not been extensively tested in patients with severe disease.Methods: A prospectively collected database was analyzed to identify patients who underwent MSA at a single institution. Individuals who had previous esophago-gastric surgery were excluded. Severe GERD was defined as lower esophageal sphincter pressure <5 mmHg, distal esophageal amplitude <30 mmHg, Barrett's metaplasia, stricture or grade C-D esophagitis, and/or DeMeester score >50. Clinical characteristics and outcomes of patients with severe GERD were compared with those of patients with mild to moderate GERD who served as control group.Results: Over the study period, a total of 336 patients met the inclusion criteria, and 102 (30.4%) had severe GERD. The median follow-up was 24 months (IQR = 75) in severe GERD patients and 32 months (IQR = 84) in those with non-severe GERD. Patients with severe GERD had a higher rate of dysphagia and higher GERD-HRQL scores. After the MSA procedure, symptoms, health-related quality of life scores, and proton-pump inhibitors consumption significantly decreased in both groups (p < 0.05). No difference between groups was found in the prevalence of severe post-operative dysphagia, the need for endoscopic dilation or device removal, and the DeMeester score.Conclusion: Laparoscopic MSA is safe and effective in reducing symptoms, PPI use, and esophageal acid exposure also in patients with severe GERD.

Highlights

  • Outcomes of laparoscopic procedures for gastroesophageal reflux disease (GERD) are variable depending on surgical expertise and/or patient-related factors

  • Throughout the years, inclusion criteria have been expanded to include patients with hiatal hernia >3 cm, esophagitis >grade B, and Barrett’s esophagus, but only a few studies have evaluated the outcomes of magnetic sphincter augmentation (MSA) in patients with severe gastro-esophageal reflux disease (GERD) [7,8,9,10,11]

  • Patients were included in the severe GERD group if one or more of the following conditions were present pre-operatively: Lower Esophageal Sphincter (LES) basal pressure

Read more

Summary

Introduction

Outcomes of laparoscopic procedures for gastroesophageal reflux disease (GERD) are variable depending on surgical expertise and/or patient-related factors. Effectiveness of laparoscopic magnetic sphincter augmentation (MSA) has not been extensively tested in patients with severe disease. The novel laparoscopic magnetic sphincter augmentation (MSA) procedure was developed to offer a minimally invasive and standardized alternative to the total (360◦) Nissen and MSA for Severe GERD the partial (270◦) Toupet fundoplication. Both total and partial fundoplication still represent the surgical standard for GERD patients who are refractory to proton-pump inhibitors (PPI) N = 102 (%). Throughout the years, inclusion criteria have been expanded to include patients with hiatal hernia >3 cm, esophagitis >grade B, and Barrett’s esophagus, but only a few studies have evaluated the outcomes of MSA in patients with severe GERD [7,8,9,10,11]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call