Vonoprazan or Proton Pump Inhibitor for Gastric Endoscopic Submucosal Dissection in Patients Taking Antithrombotic Agents

Author:

Shibata Hiroyuki1ORCID,Fujiyoshi Toshihisa2,Kawata Noboru3,Obayashi Tomohiko4,Esaki Masaya5,Kikuchi Masakazu6,Yoshida Naohiro7,Kamioka Tsuguo8,Sasaki Yoji9,Kobayashi Makoto10,Okita Muneyori11,Matsui Shigeyuki11,Furukawa Kazuhiro1ORCID,Nakamura Masanao1ORCID,Kakushima Naomi112ORCID,Fujishiro Mitsuhiro112,Kawashima Hiroki1ORCID

Affiliation:

1. Department of Gastroenterology and Hepatology Nagoya University Graduate School of Medicine Aichi Japan

2. Department of Gastroenterology Japanese Red Cross Aichi Medical Center Nagoya Daiichi Hospital Aichi Japan

3. Division of Endoscopy Shizuoka Cancer Center Shizuoka Japan

4. Department of Gastroenterology Meitetsu Hospital Aichi Japan

5. Department of Gastroenterology Handa City Hospital Aichi Japan

6. Department of Gastroenterology Yamashita Hospital Aichi Japan

7. Department of Gastroenterology Ishikawa Prefectural Central Hospital Ishikawa Japan

8. Department of Gastroenterology Kariya Toyota General Hospital Aichi Japan

9. Department of Gastroenterology Konan Kosei Hospital Aichi Japan

10. Department of Gastroenterology Yokkaichi Municipal Hospital Mie Japan

11. Department of Biostatistics Nagoya University Graduate School of Medicine Aichi Japan

12. Department of Gastroenterology The University of Tokyo Tokyo Japan

Abstract

ABSTRACTBackground and AimDelayed bleeding is a major concern after gastric endoscopic submucosal dissection (ESD), especially in patients taking antithrombotic agents. The aim of this study was to evaluate the superiority of vonoprazan (VPZ) over proton pump inhibitor (PPI) in preventing delayed bleeding after gastric ESD in patients taking antithrombotic agents.MethodsA multicenter, open‐label, randomized controlled trial was conducted in 10 Japanese centers. Gastric neoplasm patients taking antiplatelets or anticoagulants were enrolled and randomly allocated in a 1:1 ratio to either the VPZ (20 mg per day for 8 weeks) or the PPI group (esomeprazole 20 mg per day for 8 weeks). Antithrombotic agents were managed according to Japanese guidelines. The primary outcome was the delayed bleeding rate within 8 weeks after ESD. Secondary outcomes included the incidence of symptoms after ESD, healing status of ulcers at 8 weeks, safety, and factors related to delayed bleeding.ResultsOf 119 patients (59 in VPZ group, 60 in PPI group), the delayed bleeding rates were 13.6% (8/59) in the VPZ group and 8.3% (5/60) in the PPI group, with no significant difference (p = 0.36). Symptoms and adverse events, the healing status of ulcers at 8 weeks, were comparable between the groups. No use of daily antacids and the combination of antiplatelets and anticoagulants were related to delayed bleeding (odds ratio 13.1 and 34.7, p < 0.01).ConclusionThe present study did not demonstrate the superiority of VPZ over PPIs in preventing delayed bleeding after gastric ESD in patients taking antithrombotic agents.Trial Registration: (UMIN000040641/jRCTs041200045)

Publisher

Wiley

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