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Significance of wound closure after endoscopic resection for gastrointestinal lesions Yasushi Yamasaki 1 1Department of Gastroenterology, Okayama University Hospital, Okayama, Japan Keyword: clip closure , endoscopic resection pp.992-997
Published Date 2025/8/25
DOI https://doi.org/10.24479/endo.0000002166
  • Abstract
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 With advances in endoscopic techniques, it has become possible to close even large defects after endoscopic submucosal dissection (ESD). Traditionally, closure of mucosal defects was primarily considered a measure for managing intraoperative adverse events, such as bleeding or perforation. However, in recent years, it has increasingly been performed to prevent delayed adverse events, including delayed bleeding and delayed perforation. The significance and effectiveness of closure of defects after ESD vary by organ, as the incidence of intraoperative and delayed complications differs across the gastrointestinal tract. Additionally, the use of anticoagulants significantly affects the risk of post-procedural bleeding. In the colon, retrospective studies suggest that endoscopic closure after ESD reduces the risk of delayed bleeding. However, RCTs have not shown significant differences, necessitating further large-scale studies. Among patients taking anticoagulants, closure of mucosal defects after ESD appears to reduce the risk of bleeding. In the duodenum, closure of defects after ESD/EMR is particularly beneficial and is recommended by ESGE guidelines, as studies indicate a significant reduction in delayed bleeding and delayed perforation. In the stomach, maintaining closure is challenging, and its effectiveness in preventing adverse events remains uncertain. However, novel closure methods, such as endoscopic suturing and O-ring techniques, have shown promise in reducing delayed bleeding, especially in patients on anticoagulants. The significance of endoscopic closure of defects varies by organ, and careful consideration of patient background is essential when determining its necessity for preventing delayed adverse events.


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電子版ISSN 印刷版ISSN 0915-3217 東京医学社

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