PMID- 16905695 OWN - NLM STAT- MEDLINE DCOM- 20060921 LR - 20181113 IS - 0017-5749 (Print) IS - 1468-3288 (Electronic) IS - 0017-5749 (Linking) VI - 55 IP - 9 DP - 2006 Sep TI - A randomised controlled trial of ablation of Barrett's oesophagus with multipolar electrocoagulation versus argon plasma coagulation in combination with acid suppression: long term results. PG - 1233-9 AB - BACKGROUND: Many modalities have been used to ablate Barrett's oesophagus (BO). However, long term results and comparative effectiveness are unknown. AIMS: Our aim was to compare the long term efficacy of achieving complete reversal (endoscopic and histological) between multipolar electrocoagulation (MPEC) and argon plasma coagulation (APC) in BO patients and assess factors influencing successful ablation. METHODS: Patients with BO, 2-6 cm long, underwent 24 hour pH testing on proton pump inhibitor (PPI) therapy. Patients were then randomised by BO length to undergo ablation with MPEC or APC every 4-8 weeks until endoscopic reversal or maximal of six treatment sessions. RESULTS: Thirty five BO patients have been followed for at least two years following endoscopic ablation, 16 treated with MPEC and 19 with APC. There was complete reversal of BO in 24 patients (69%); 75% with MPEC and 63% with APC (p = 0.49). There was no difference in the number of sessions required in the two groups. There was no difference in age, pH results, BO length, PPI dose, or hiatal hernia size between patients with and without complete reversal. One patient developed an oesophageal stricture but there were no major complications such as bleeding or perforation. CONCLUSIONS: In BO patients treated with MPEC or APC in combination with acid suppression, at long term follow up, complete reversal of BO can be maintained in approximately 70% of patients, irrespective of the technique. There are no predictors associated with achieving complete reversal of BO. Continued surveillance is still indicated in the post ablative setting. As yet, these techniques are not ready for clinical application (other than for high grade dysplasia or early oesophageal adenocarcinoma) and cannot be offered outside the research arena. FAU - Sharma, P AU - Sharma P AD - University of Kansas School of Medicine and Veterans Affairs Medical Center, Kansas City, MO 64128-2295, USA. psharma@kumc.edu FAU - Wani, S AU - Wani S FAU - Weston, A P AU - Weston AP FAU - Bansal, A AU - Bansal A FAU - Hall, M AU - Hall M FAU - Mathur, S AU - Mathur S FAU - Prasad, A AU - Prasad A FAU - Sampliner, R E AU - Sampliner RE LA - eng PT - Comparative Study PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, Non-P.H.S. PL - England TA - Gut JT - Gut JID - 2985108R RN - 0 (Antacids) RN - 0 (Proton Pump Inhibitors) SB - IM CIN - Gut. 2006 Sep;55(9):1222-3. PMID: 16905690 CIN - Gut. 2007 Jun;56(6):884-5; author reply 885. PMID: 17519491 MH - Adult MH - Aged MH - Aged, 80 and over MH - Antacids/therapeutic use MH - Barrett Esophagus/drug therapy/pathology/*surgery MH - Combined Modality Therapy MH - Electrocoagulation/adverse effects/*methods MH - Esophageal Neoplasms/drug therapy/pathology/*surgery MH - Esophagoscopy/methods MH - Female MH - Follow-Up Studies MH - Humans MH - Hydrogen-Ion Concentration MH - Laser Coagulation/adverse effects/*methods MH - Male MH - Middle Aged MH - Monitoring, Physiologic MH - Precancerous Conditions/drug therapy/pathology/*surgery MH - Prognosis MH - Proton Pump Inhibitors MH - Treatment Outcome PMC - PMC1860010 COIS- Conflict of interest: None declared. EDAT- 2006/08/15 09:00 MHDA- 2006/09/22 09:00 PMCR- 2009/09/01 CRDT- 2006/08/15 09:00 PHST- 2006/08/15 09:00 [pubmed] PHST- 2006/09/22 09:00 [medline] PHST- 2006/08/15 09:00 [entrez] PHST- 2009/09/01 00:00 [pmc-release] AID - 55/9/1233 [pii] AID - gt86777 [pii] AID - 10.1136/gut.2005.086777 [doi] PST - ppublish SO - Gut. 2006 Sep;55(9):1233-9. doi: 10.1136/gut.2005.086777.