Cammarota G, Cannizzaro O, Ojetti V, Cianci R, Pastorelli A, Armuzzi A, Gentiloni N, Gasbarrini A, Pirozzi G, Gasbarrini G
Department of Internal Medicine and Gastroenterology, Catholic University of Rome, Italy.
Aliment Pharmacol Ther. 2000 Jan;14(1):73-7. doi: 10.1046/j.1365-2036.2000.00664.x.
Ranitidine bismuth citrate (RBC)-based triple therapies for a period of 7 days have proved to be an effective treatment for Helicobacter pylori.
To investigate the eradication efficacy, safety profile and patient compliance of two RBC-based triple therapies given for 5 days.
Eighty H. pylori-positive patients with dyspeptic symptoms, referred to us for gastroscopy, were consecutively enrolled in this prospective, randomized, open-label study. These patients were randomly assigned to receive a 5-day course of RBC 400 mg b.d. plus clarithromycin 500 mg b.d. and either tinidazole 500 mg b.d. (RBCCT group) or amoxycillin 1 g b.d. (RBCCA group). The H. pylori status was assessed by means of histology and rapid urease test at entry, and by 13C-urea breath test 8 weeks after the completion of treatment.
All enrolled patients completed the study. Thirty-seven of 40 patients treated with RBCCT (both PP and ITT analysis: 93%; 95% CI: 80-98%) and 35 of 40 in the RBCCA group (both PP and ITT analysis: 88%; 95% CI: 73-96%) returned H. pylori-negative. Slight or mild side-effects occurred in 4/40 patients (10%) in the RBCCT group and in 5/40 (12%) in the RBCCA group.
This is the first study demonstrating the efficacy of RBC-based triple therapies given for only 5 days. RBC regimens containing high-dose clarithromycin and either amoxycillin or tinidazole prove to be well tolerated, safe and preserve good eradication rates even when administered for a shorter than conventional duration.
基于枸橼酸铋雷尼替丁(RBC)的三联疗法治疗7天已被证明是治疗幽门螺杆菌的有效方法。
研究两种基于RBC的三联疗法治疗5天的根除疗效、安全性和患者依从性。
80例有消化不良症状且因胃镜检查转诊至我院的幽门螺杆菌阳性患者连续纳入这项前瞻性、随机、开放标签研究。这些患者被随机分配接受为期5天的RBC 400 mg,每日2次,加克拉霉素500 mg,每日2次,以及替硝唑500 mg,每日2次(RBCCT组)或阿莫西林1 g,每日2次(RBCCA组)。在入组时通过组织学和快速尿素酶试验评估幽门螺杆菌状态,并在治疗完成后8周通过13C尿素呼气试验评估。
所有入组患者均完成研究。RBCCT组40例患者中有37例(PP和ITT分析均为:93%;95%CI:80-98%),RBCCA组40例中有35例(PP和ITT分析均为:88%;95%CI:73-96%)幽门螺杆菌检测呈阴性。RBCCT组4/40患者(10%)和RBCCA组5/40患者(12%)出现轻微或轻度副作用。
这是第一项证明基于RBC的三联疗法仅治疗5天有效的研究。含高剂量克拉霉素和阿莫西林或替硝唑的RBC方案即使给药时间短于传统疗程,也被证明耐受性良好、安全且保持良好的根除率。