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A prospective study of endoscopic radiofrequency application (STRETTA) for gastroesophageal reflux disease: Early UK experience N Hamza, D Kamali, S Punnoose,

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Presentation on theme: "A prospective study of endoscopic radiofrequency application (STRETTA) for gastroesophageal reflux disease: Early UK experience N Hamza, D Kamali, S Punnoose,"— Presentation transcript:

1 A prospective study of endoscopic radiofrequency application (STRETTA) for gastroesophageal reflux disease: Early UK experience N Hamza, D Kamali, S Punnoose, A Dhar, A Reddy, YKS Viswanath Department of Surgery, James Cook University Hospital, Middlesbrough, United Kingdom Introduction Radiofrequency application (RFA) is considered appropriate therapy for patients with gastroesophageal reflux disease (GERD) (SAGES 2013) It produces symptomatic relief in patients with GERD (UK NICE guidance 2013) Aim k The objective of the current study is to present our early UK experience of patients undergoing RFA for GERD Methods & procedures A prospective study All patients underwent upper gastrointestinal endoscopy and barium meal as part of preoperative work up Transoral device to deliver RFA to the oesophageal wall at the GOJ, under sedation or GA 30-mm diameter balloon with 4 electrodes to generate a tissue temperature of 65oC to 85oC during a series of one-minute treatment cycles (Fig 1, 2) Data presented as median (interquartile range, IQR) Fig 2: Endoscopic appearance pre and post RFA Endoscopic and post-RFA outcomes: Hiatus hernia (<2cm) 6/19 (32%) Anesthesia: General Conscious sedation 8/19 11/19 RFA was delivered at all 6 levels in all patients with a median (IQR) of 50 (44-54), out of possible 56, treatment points achieving more than 30 seconds cycle Postoperative complications 0 (0%) Follow up 4 (2-6) months Post-RFA GERD score*: Heartburn Dysphagia Regurgitation 1 (0-1) 0 (0-1) 0 (0-2) Results Preoperative characteristics: Study period Oct 14 - Aug 15 Number of patients 19 Sex: Female (%) 12/19 (63%) Age (year) 62 (52-65) Previous antireflux surgery 4/19 (21%) Pre-RFA GERD score*: Heartburn Dysphagia Regurgitation 4 (3.5-4) 2 (0-4) 4 (3-4) *(0=no symptoms, 1=symptoms noticeable but not bothersome, 2= symptoms bothersome but not every day, 3=symptoms bothersome every day, 4=symptoms affect daily activity, and 5=incapacitating symptoms) Conclusion RFA is feasible and safe in the treatment of symptomatic GERD In short term, it achieves symptomatic relief in the majority of patients In patients with poor response to medical therapy, it can be considered as an alternative option to surgery in those who are unfit for surgical intervention Long term follow up is essential to appraise the durability of these favourable outcomes *(0=no symptoms, 1=symptoms noticeable but not bothersome, 2= symptoms bothersome but not every day, 3=symptoms bothersome every day, 4=symptoms affect daily activity, and 5=incapacitating symptoms) (Fig 1: Balloon with four 5.5-mm retractable stylet electrodes delivering a series of one-minute treatment cycles


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