首页> 美国卫生研究院文献>Canadian Journal of Gastroenterology >Vonoprazan-Based Regimen Is More Useful than PPI-Based One as a First-Line Helicobacter pylori Eradication: A Randomized Controlled Trial
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Vonoprazan-Based Regimen Is More Useful than PPI-Based One as a First-Line Helicobacter pylori Eradication: A Randomized Controlled Trial

机译:基于Vonoprazan的治疗方案比基于PPI的治疗方案更有用作为根除幽门螺杆菌的一线药物:一项随机对照试验

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摘要

Background. A new agent, potassium-competitive acid blocker vonoprazan (VPZ) has potent acid-inhibitory effects and may offer advantages over conventional H. pylori eradication therapies. We aimed to compare the eradication rate between VPZ-based treatment and PPI-based one. Methods. This randomized controlled trial was designed to assign 141 patients with H. pylori-positive gastritis to VPZ group (VPZ 20 mg, amoxicillin 750 mg, and clarithromycin 200 or 400 mg twice daily for 7 days) or PPI group (rabeprazole 20 mg or lansoprazole 30 mg, amoxicillin 750 mg, and clarithromycin 200 or 400 mg twice daily for 7 days). Primary endpoints were eradication rates and adverse events. Results. Seventy of 72 patients in VPZ group and 63 of 69 patients in PPI group completed the treatment after 7 days. The eradication rate was significantly higher in VPZ group than PPI group by intention-to-treat analysis (95.8% versus 69.6%, P = 0.00003, 95% confidence interval [CI] 88.3-99.1% versus 57.3-80.1%) and per-protocol analysis (95.7% versus 71.4%, P = 0.0002, 95% CI 88.0-99.1% versus 58.7-82.1%). The incidence of adverse events was not different between the groups (26.3% in VPZ group versus 37.7% in PPI group, P = 0.15). Conclusion. VPZ-based regimen is more useful than that PPI-based regimen as a first-line H. pylori eradication therapy.
机译:背景。一种新型的钾竞争性酸阻滞剂vonoprazan(VPZ)具有强效的酸抑制作用,并且可能比传统的幽门螺杆菌根除疗法更具优势。我们旨在比较基于VPZ的治疗和基于PPI的治疗的根除率。方法。该随机对照试验旨在将141例幽门螺杆菌阳性胃炎患者分配到VPZ组(VPZ 20 mg,阿莫西林750 mg和克拉霉素200或400 mg,每天两次,共7天)或PPI组(雷贝拉唑20 mg或兰索拉唑30毫克,阿莫西林750毫克和克拉霉素200或400毫克,每天两次,共7天)。主要终点是根除率和不良事件。结果。 7天后,VPZ组的72名患者中有70名,PPI组的69名患者中有63名完成了治疗。通过意向性治疗分析,VPZ组的根除率显着高于PPI组(95.8%对69.6%,P = 0.00003,95%置信区间[CI] 88.3-99.1%对57.3-80.1%),并且方案分析(95.7%对71.4%,P = 0.0002,95%CI 88.0-99.1%对58.7-82.1%)。各组之间不良事件的发生率没有差异(VPZ组为26.3%,PPI组为37.7%,P = 0.15)。结论。基于VPZ的方案比基于PPI的方案作为一线幽门螺杆菌根除疗法更有用。

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