首页> 外文期刊>European journal of gastroenterology and hepatology >A randomized trial of standard-dose versus half-dose rabeprazole, clarithromycin, and amoxicillin in the treatment of Helicobacter pylori infection.
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A randomized trial of standard-dose versus half-dose rabeprazole, clarithromycin, and amoxicillin in the treatment of Helicobacter pylori infection.

机译:标准剂量和半剂量雷贝拉唑,克拉霉素和阿莫西林治疗幽门螺杆菌感染的随机试验。

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OBJECTIVES: To evaluate the efficacy and safety of a standard-dose versus half-dose 10-day triple regimen for the eradication of Helicobacter pylori infection. METHODS: A total of 115 consecutive patients with documented infection were enrolled in this open-label trial. Group A (standard dose) received rabeprazole (20 mg), amoxicillin (1 g), and clarithromycin (500 mg), all twice daily for 10 days. Group B (half dose) received rabeprazole (10 mg), amoxicillin (500 mg), and clarithromycin (250 mg), all twice daily for 10 days. (14)C urea breath tests were performed a minimum of 4 weeks after treatment and a minimum of 2 weeks off any acid-suppressive therapy. Compliance and adverse effects were evaluated throughout the treatment period. RESULTS: A total of 115 patients were enrolled (59 women and 56 men; mean age 47.1+/-14.0 years). Eradication occurred in 45 of 58 patients [77.6%; 95% confidence interval (CI): 66.9-88.3%] in the standard-dose group versus 44 of 57 in the half-dose group (77.2%; 95% CI: 66.3-88.1%) on an intent-to-treat (ITT) analysis (P=1.00). Per protocol eradication rates were 45 of 57 (78.9%; 95% CI: 68.4-85.9%) and 44 of 54 (81.5%; 95% CI: 71.1-91.8%), respectively (P=0.81). The number of patients reporting any adverse effect was significantly higher in the standard-dose group (64.9 vs. 40.4%; P=0.014). The cost of treatment was significantly less in patients receiving the half-dose regimen (ITT analysis; P<0.05). The number needed to harm to suffer one additional failure in the half-dose over the standard-dose arm was 250 (ITT analysis). CONCLUSION: A half-dose 10-day regimen of rabeprazole, amoxicillin, and clarithromycin is equally effective but cheaper and better tolerated than its standard-dose regimen in the treatment of Helicobacter pylori. Eradication rates of both regimens are, however, suboptimal compared with accepted standards.
机译:目的:评估标准剂量和半剂量10天三联疗法根除幽门螺杆菌感染的疗效和安全性。方法:该开放标签试验共纳入115名连续的有文件证明感染的患者。 A组(标准剂量)接受雷贝拉唑(20 mg),阿莫西林(1 g)和克拉霉素(500 mg),每天两次,共10天。 B组(半剂量)接受雷贝拉唑(10 mg),阿莫西林(500 mg)和克拉霉素(250 mg),每天两次,共10天。 (14)C尿素呼气试验在治疗后至少4周进行,并且在任何酸抑制治疗后至少进行2周。在整个治疗期间评估依从性和不良反应。结果:共纳入115名患者(59名女性和56名男性;平均年龄47.1 +/- 14.0岁)。 58例患者中有45例根除[77.6%;在意向性治疗中,标准剂量组的95%置信区间(CI):66.9-88.3%,而半剂量组的57个可信区间(CI):57个中的44个(77.2%; 95%CI:66.3-88.1%)( ITT)分析(P = 1.00)。每个方案的根除率分别为57中的45(78.9%; 95%CI:68.4-85.9%)和54中的44(81.5%; 95%CI:71.1-91.8%)(P = 0.81)。在标准剂量组中,报告有任何不良反应的患者数量显着更高(64.9 vs. 40.4%; P = 0.014)。接受半剂量方案的患者的治疗费用显着降低(ITT分析; P <0.05)。在标准剂量组的半剂量中,需要遭受另一半失败而遭受伤害的伤害数量为250(ITT分析)。结论:雷贝拉唑,阿莫西林和克拉霉素半剂量的10天治疗方案在治疗幽门螺杆菌方面同样有效,但比其标准剂量方案更便宜且耐受性更好。然而,与接受的标准相比,两种方案的根除率都不理想。

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