Minimal access surgery compared with medical management for chronic gastro-oesophageal reflux disease: UK collaborative randomised trial

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dc.contributor.author Grant, AM en
dc.contributor.author Wileman, SM en
dc.contributor.author Ramsay, CR en
dc.contributor.author Mowat, NA en
dc.contributor.author Krukowski, ZH en
dc.contributor.author Heading, RC en
dc.contributor.author Thursz, MR en
dc.contributor.author Campbell, MK en
dc.contributor.author REFLUX Trial Group en
dc.date.accessioned 2012-02-23T02:16:55Z en
dc.date.issued 2008-12-15 en
dc.identifier.citation BMJ 337(a2664):1-8 15 Dec 2008 en
dc.identifier.issn 0959-8138 en
dc.identifier.uri http://hdl.handle.net/2292/11830 en
dc.description.abstract Objective To determine the relative benefits and risks of laparoscopic fundoplication surgery as an alternative to long term drug treatment for chronic gastro-oesophageal reflux disease (GORD). Design Multicentre, pragmatic randomised trial (with parallel preference groups). Setting 21 hospitals in the United Kingdom. Participants 357 randomised participants (178 surgical, 179 medical) and 453 preference participants (261, 192); mean age 46; 66% men. All participants had documented evidence of GORD and symptoms for >12 months. Intervention The type of laparoscopic fundoplication used was left to the discretion of the surgeon. Those allocated to medical treatment had their treatment reviewed and adjusted as necessary by a local gastroenterologist, and subsequent clinical management was at the discretion of the clinician responsible for care. Main outcome measures The disease specific REFLUX quality of life score (primary outcome), SF-36, EQ-5D, and medication use, measured at time points equivalent to three and 12 months after surgery, and surgical complications. Main results Randomised participants had received drugs for GORD for median of 32 months before trial entry. Baseline REFLUX scores were 63.6 (SD 24.1) and 66.8 (SD 24.5) in the surgical and medical randomised groups, respectively. Of those randomised to surgery, 111 (62%) actually had total or partial fundoplication. Surgical complications were uncommon with a conversion rate of 0.6% and no mortality. By 12 months, 38% (59/154) randomised to surgery (14% (14/104) among those who had fundoplication) were taking reflux medication versus 90% (147/164) randomised medical management. The REFLUX score favoured the randomised surgical group (14.0, 95% confidence interval 9.6 to 18.4; P<0.001). Differences of a third to half of 1 SD in other health status measures also favoured the randomised surgical group. Baseline scores in the preference for surgery group were the worst; by 12 months these were better than in the preference for medical treatment group. Conclusion At least up to 12 months after surgery, laparoscopic fundoplication significantly increased measures of health status in patients with GORD. Trial registration ISRCTN15517081. en
dc.publisher BMJ Publishing Group Ltd. en
dc.relation.ispartofseries BMJ en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from http://www.sherpa.ac.uk/romeo/issn/0959-8138/ en
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm en
dc.title Minimal access surgery compared with medical management for chronic gastro-oesophageal reflux disease: UK collaborative randomised trial en
dc.type Journal Article en
dc.identifier.doi 10.1136/bmj.a2664 en
pubs.issue a2664 en
pubs.begin-page 1 en
pubs.volume 337 en
dc.rights.holder Copyright: BMJ Publishing Group Ltd. en
pubs.author-url http://www.bmj.com/content/337/bmj.a2664.full.pdf+html en
pubs.end-page 8 en
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Article en
pubs.elements-id 187919 en
pubs.record-created-at-source-date 2010-11-29 en


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