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DC Field | Value | Language |
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dc.contributor.author | Brown, Gregor | - |
dc.contributor.other | Pellise, Maria | - |
dc.contributor.other | Burgess, Nicholas | - |
dc.contributor.other | Tutticci, Nicholas | - |
dc.contributor.other | Hourigan, Luke | - |
dc.contributor.other | Zanati, Simon | - |
dc.contributor.other | Singh, Rajvinder | - |
dc.contributor.other | Williams, Stephen | - |
dc.contributor.other | Raftopoulos, Spiro | - |
dc.contributor.other | Ormonde, Donald | - |
dc.contributor.other | Moss, Alan | - |
dc.contributor.other | Byth, Karen | - |
dc.contributor.other | P'Ng, Heok | - |
dc.contributor.other | Mahajan, Hema | - |
dc.contributor.other | McLeod, Duncan | - |
dc.contributor.other | Bourke, Michael | - |
dc.date | 2016-01 | - |
dc.date.accessioned | 2016-05-11T03:57:33Z | - |
dc.date.available | 2016-05-11T03:57:33Z | - |
dc.date.issued | 2016-01 | - |
dc.identifier.citation | Gut. 2016 Jan 19. pii: [Epub ahead of print] | en_US |
dc.identifier.issn | 1468-3288 | en_US |
dc.identifier.uri | http://hdl.handle.net/11434/648 | - |
dc.description.abstract | OBJECTIVE: Endoscopic mucosal resection (EMR) is effective for large laterally spreading flat and sessile lesions (LSLs). Sessile serrated adenomas/polyps (SSA/Ps) are linked to the relative failure of colonoscopy to prevent proximal colorectal cancer. We aimed to examine the technical success, adverse events and recurrence following EMR for large SSA/Ps in comparison with large conventional adenomas. DESIGN: Over 74 months till August 2014, prospective multicentre data of LSLs ≥20 mm were analysed. A standardised dye-based conventional EMR technique followed by scheduled surveillance colonoscopy was used. RESULTS: From a total of 2000 lesions, 323 SSA/Ps in 246 patients and 1527 adenomas in 1425 patients were included for analysis. Technical success for EMR was superior in SSA/Ps compared with adenomas (99.1% vs 94.5%, p<0.001). Significant bleeding and perforation were similar in both cohorts. The cumulative recurrence rates for adenomas after 6, 12, 18 and 24 months were 16.1%, 20.4%, 23.4% and 28.4%, respectively. For SSA/Ps, they were 6.3% at 6 months and 7.0% from 12 months onwards (p<0.001). Following multivariable adjustment, the HR of recurrence for adenomas versus SSA/Ps was 1.7 (95% CI 0.9 to 3.0, p=0.097). Subgroup analysis by lesion size revealed an eightfold increased risk of recurrence for 20-25 mm adenomas versus SSA/Ps, but no significantly different risk between lesion types in larger lesion groups. CONCLUSION: Recurrence after EMR of 20-25 mm LSLs is significantly less frequent in SSA/Ps compared with adenomatous lesions. SSA/Ps can be more effectively removed than adenomatous LSLs with equivalent safety. Ensuring complete initial resection is imperative for avoiding recurrence. TRIAL REGISTRATION NUMBER: ClinicalTrials.gov NCT01368289. | en_US |
dc.publisher | British Society of Gastroenterology, and BMJ | en_US |
dc.subject | Department of Gastroenterology and Hepatology, Epworth HealthCare, Victoria, Australia | en_US |
dc.subject | Endoscopic Mucosal Resection | en_US |
dc.subject | EMR | en_US |
dc.subject | Colonic Polyps | en_US |
dc.subject | Colonoscopy | en_US |
dc.subject | Colorectal Adenomas | en_US |
dc.subject | Colorectal Cancer | en_US |
dc.subject | Endoscopic Procedures | en_US |
dc.subject | Laterally Spreading Flat and Sessile Lesions | en_US |
dc.subject | LSLs | en_US |
dc.subject | Sessile Serrated Adenomas/ Polyps | en_US |
dc.subject | SSA/Ps | en_US |
dc.subject | Large Conventional Adenomas | en_US |
dc.subject | Gastroenterology | en_US |
dc.title | Endoscopic mucosal resection for large serrated lesions in comparison with adenomas: a prospective multicentre study of 2000 lesions. | en_US |
dc.type | Journal Article | en_US |
dc.identifier.doi | 10.1136/gutjnl-2015-310249 | en_US |
dc.identifier.journaltitle | Gut | en_US |
dc.description.pubmeduri | http://www.ncbi.nlm.nih.gov/pubmed/26786685 | en_US |
dc.description.affiliates | Departments of Gastroenterology and Hepatology, Westmead Hospital, Sydney, New South Wales, Australia. | en_US |
dc.description.affiliates | Westmead Clinical School, University of Sydney, Sydney, New South Wales, Australia. | en_US |
dc.description.affiliates | Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Queensland, Australia. | en_US |
dc.description.affiliates | Department of Gastroenterology and Hepatology, Greenslopes Private Hospital, Brisbane, Queensland, Australia. | en_US |
dc.description.affiliates | Department of Gastroenterology and Hepatology, The Alfred Hospital, Melbourne, Victoria, Australia | en_US |
dc.description.affiliates | Department of Gastroenterology and Hepatology, Western Hospital, Melbourne, Victoria, Australia. | en_US |
dc.description.affiliates | Department of Gastroenterology and Hepatology, Lyell McEwin Hospital, Adelaide, South Australia, Australia. | en_US |
dc.description.affiliates | Department of Gastroenterology and Hepatology, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia. | en_US |
dc.description.affiliates | NHMRC Clinical Trials Centre, University of Sydney, Sydney, New South Wales, Australia. | en_US |
dc.description.affiliates | Research and Education Network, Westmead Hospital, Sydney, New South Wales, Australia. | en_US |
dc.description.affiliates | Institute of Clinical Pathology and Medical Research, Westmead Hospital, Sydney, New South Wales, Australia. | en_US |
dc.type.studyortrial | Multicentre Studies | en_US |
dc.type.contenttype | Text | en_US |
Appears in Collections: | Cancer Services General Surgery and Gastroenterology |
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