4.6 Article

Efficacy of hemostatic powder in preventing bleeding after gastric endoscopic submucosal dissection in high-risk patients

Journal

JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
Volume 33, Issue 3, Pages 656-663

Publisher

WILEY
DOI: 10.1111/jgh.13990

Keywords

adverse event; antithrombotic therapy; endoscopic submucosal dissection; hemostatic powder; high risk of bleeding; post-ESD bleeding

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Background and AimThe prevention of post-endoscopic submucosal dissection (ESD) bleeding in high-risk patients is an important problem. This study evaluated the efficacy of polysaccharide hemostatic powder in preventing post-ESD bleeding in high-risk patients. MethodsPatients at high risk for post-ESD bleeding were prospectively enrolled between December 2015 and July 2016. A high risk of post-ESD bleeding was considered if the patients were taking antithrombotic agents or had undergone a large resection (specimen size 40mm). The endpoints were Forrest classification of the post-ESD ulcer on second-look endoscopy 2days after the procedure and bleeding rates within 48h and at 4weeks. ResultsForty-four patients underwent gastric ESD and treatment with hemostatic powder. Among them, 33 patients (70.5%) underwent large resection (40mm) without antithrombotic therapy, and 13 patients (29.5%) received antithrombotic therapy. The mean resected specimen size was 55.313.9mm. The proportion of high-risk delayed bleeding lesions (Forrest IIa) at second-look endoscopy was 4.5% (2/44). The overall bleeding rate was 9.1% (4/44). There was no early bleeding event. The median (interquartile range) timing of bleeding after the procedure was 12.5 (interquartile range 10.3-15.5) days. The bleeding rate in the large resection (40mm) group without antithrombotic therapy and the antithrombotic therapy group was 3.2% (1/33) and 23.1% (3/13), respectively. ConclusionsHemostatic powder may be a promising new simple and effective method to prevent early post-ESD bleeding in high-risk patients, especially for those with larger resection. (Clinical trial registration number: NCT02625792).

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