实用医学杂志 ›› 2022, Vol. 38 ›› Issue (10): 1271-1275.doi: 10.3969/j.issn.1006⁃5725.2022.10.019

• 药物与临床 • 上一篇    下一篇

伏诺拉生联合阿莫西林、克拉霉素三联七日疗法根除幽门螺杆菌的临床研究

王先令 周国强 林琳 金成范 苏剑东 刘思纯    

  1. 东莞松山湖东华医院消化内科(广东东莞 523000)

  • 出版日期:2022-05-25 发布日期:2022-05-25
  • 通讯作者: 刘思纯 E⁃mail:Liusichun66@sina.com

Clinical study on the eradication of Helicobacter pylori by vonolaxan combined with amoxicillin and clar⁃ ithromycin for seven⁃day triple therapy

WANG Xianling,ZHOU Guoqiang,LIN Lin,JIN Chengfan,SU Jian⁃ dong,LIU Sichun.   

  1. Department of Gastroenterology,Dongguan Songshan Lake Tungwah Hospital,Dongguan 523000,China

  • Online:2022-05-25 Published:2022-05-25
  • Contact: LIU Sichun E⁃mail:Liusichun66@sina.com

摘要:

目的 探讨伏诺拉生联合阿莫西林、克拉霉素三联七日疗法根除幽门螺杆菌(Helicobacter pyloriHp)的临床效果和安全性。方法 选取东莞松山湖东华医院自 2021 6 月至 2021 12 月诊断 Hp 感染患者 200 例,随机分为研究组 100 例和对照组 100 例,研究组接受伏诺拉生联合阿莫西林、克拉霉素三 联七日疗法,对照组接受标准四联两周疗法,所有患者均在停药至少 4 周后再次接受 13C 尿素呼气试验检 查,比较两组患者的一般资料、不良反应、Hp 根除率和费用情况。结果 研究组和对照组因失访和中途退 出研究例数分别为 18 例和 17 例,最终得到研究组样本 82 例,对照组样本 83 例。两组患者在年龄和性别 一般资料方面比较差异无统计学意义(P > 0.05)。不良反应方面,研究组总体发生率为 7.3%,与对照组的 12.0%比较,差异无统计学意义(χ2 = 1.054,P = 0.305)。研究组中,意向性治疗(intention to treat,ITT)分析 Hp 根除率为 74.0%(74/100)、符合方案集(per protocol,PP)分析 Hp 根除率为 90.2%(74/82)。对照组中,ITT Hp 根除率为 72.0%(72/100)、PP 分析 Hp 根除率为 86.7%(72/83)。两组间 ITT 分析 Hp 根除率(χ2 = 0.101 P = 0.750)和 PP 分析 Hp 根除率(χ2 = 0.495,P = 0.482)比较,差异均无统计学意义(P > 0.05)。结论 伏诺 拉生联合阿莫西林、克拉霉素三联七日疗法根除Hp效果确切、安全,值得临床推广。

关键词:

伏诺拉生, 质子泵抑制剂, 幽门螺杆菌

Abstract:

Objective To investigate the clinical effect and safety of vonolaxan combined with amoxicillin and clarithromycin for seven⁃day eradication of Helicobacter pylori(Hp). Methods A total of 200 patients with Hp infection diagnosed in Dongguan Songshan Lake Tungwah Hospital from June 2021 to December 2021 were selected and randomly divided into a study group of 100 cases and a control group of 100 cases. The study group received Vonolaxan combined with amoxicillin and clarithromycin triple therapy for seven days ,while the control group received standard quadruple therapy for 2 weeks. All patients received carbon 13 breath test again after at least 4 weeks of drug. The general data,adverse reactions,Hp eradication rate and cost of the two groups of patients were compared. Results The number of cases in the study group and control group were 18 and 17 due to loss to follow⁃up and drop out of the study,respectively. In the end,82 samples in the study group and 83 samples in the control group were obtained. There was no statistical difference in the general data of age and gender between the two groups(P > 0.05). In terms of adverse reactions,the overall incidence rate of the study group was 7.3% compared with 12.0% of the control group,the difference was not statistically significant(χ2 = 1.054,P = 0.305). In the study group,the eradication rate of Hp was 74.0%(74/100)by intention to treat(ITT)analysis and 90.2% (74/82)by per protocol(PP)analysis. In the control group,the eradication rate of Hp was 72.0%(72/100)by ITT analysis and 86.7%(72/83)by PP analysis. There was no significant difference between the two groups in the eradication rate of Hp by ITT(χ2 = 0.101,P = 0.750)and PP analysis(χ2 = 0.495,P = 0.482)(P > 0.05). Conclusions Vonolaxan combined with amoxicillin and clarithromycin triple therapy for seven days is effective and safe in eradicating Hp,which is worthy of widespread clinical promotion.

Key words: vonolaxan,  , proton pump inhibitor,  , helicobacter pylori