4.8 Article

Scheduled second-look endoscopy is not recommended after endoscopic submucosal dissection for gastric neoplasms (the SAFE trial): a multicentre prospective randomised controlled non-inferiority trial

Journal

GUT
Volume 64, Issue 3, Pages 397-405

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/gutjnl-2014-307552

Keywords

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Funding

  1. Astellas Pharmaceutical
  2. Takeda Pharmaceutical
  3. Zeria Pharmaceutical
  4. Otsuka Pharmaceutical
  5. AstraZeneca Pharmaceutical
  6. Dainihon-Sumitomo Pharmaceutical
  7. Taiho Pharmaceutical
  8. Ajinomoto Pharmaceutical
  9. Daiichi-Sankyo Pharmaceutical
  10. Aska Pharmaceutical
  11. Eisai
  12. Grants-in-Aid for Scientific Research [25460381] Funding Source: KAKEN

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Objective To clarify the effectiveness of second-look endoscopy (SLE) at preventing bleeding after gastric endoscopic submucosal dissection (ESD). Design A multicentre prospective randomised controlled non-inferiority trial was conducted at five referral institutions across Japan. Patients with a solitary gastric neoplasm were enrolled. Exclusion criteria were previous oesophagogastric surgery or radiation therapy; perforation and the administration of antithrombotics, steroids or non-steroidal anti-inflammatory drugs. Patients were assigned to the SLE group or the non-SLE group by a computer-generated random sequence after ESD and were treated perioperatively with a proton pump inhibitor. SLE was performed one day after ESD. The primary endpoint was post-ESD bleeding, defined as an endoscopically proven haemorrhage. The trial had the power to detect a non-inferiority criterion of 7% between the groups. Results From February 2012 to February 2013, 130 and 132 patients were assigned to the SLE and the non-SLE groups, respectively. All patients were included in the intention-to-treat analysis of the primary endpoint. Post-ESD bleeding occurred in seven patients with (5.4%) SLE and five patients with (3.8%) non-SLE (risk difference -1.6% (95% CI -6.7 to 3.5); p(non-inferiority)<0.001), meeting the non-inferiority criterion. All 12 patients with post-ESD bleeding and one patient with a delayed perforation were successfully managed with conservative treatment. Conclusions SLE after gastric ESD is not routinely recommended because it does not contribute to the prevention of post-ESD bleeding for patients with an average bleeding risk.

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