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首页> 外文期刊>European journal of gastroenterology and hepatology >Optimal duration of concomitant nonbismuth quadruple therapy as first-line therapy for Helicobacter pylori: a prospective, open-label, comparative study
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Optimal duration of concomitant nonbismuth quadruple therapy as first-line therapy for Helicobacter pylori: a prospective, open-label, comparative study

机译:作为幽门螺杆菌幽门螺杆菌的一线治疗的伴随性非铋疗法的最佳持续时间:前瞻性,开放标签,比较研究

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Background Concomitant nonbismuth quadruple therapy is recommended as first-line treatment for Helicobacter pylori infection in high clarithromycin resistance areas, but the ideal duration of the regimen remains elusive. Aim of this study was to assess the efficacy and tolerability of 10- versus 14-day concomitant therapy for H. pylori eradication in an area of high clarithromycin and low dual clarithromycin/metronidazole resistance. Methods This was a prospective, open-label study including adult patients with H. pylori infection without previous treatment, from September 2014 to June 2017. Concomitant therapy consisting of pantoprazole 40 mg, amoxicillin 1g, clarithromycin 500 mg, and a nitroimidazole 500 mg was administered twice daily for 10 days in the first phase and for 14 days in the second phase of the study. Efficacy and side effects were compared between groups using chi-square and Fisher's exact tests. Results In per protocol analysis, rates of eradication for the 10- and 14-day regimen were 91.9% (114/124) and 90.9% (110/121), respectively (P = 0.77). In intention to treat analysis, rates of eradication were lower than 90%. Specifically, rates were 86.3% (114/132) for the 10-day regimen and 85.2% (110/129) for the 14-day regimen (P = 0.8). Side effects, present in 31.3% of treated patients, were significantly more common in the 14-day group (P = 0.015). Four patients discontinued treatment, all in the 14-day group. Conclusions Ten day concomitant nonbismuth quadruple therapy for H. pylori is highly efficacious and better tolerated than the 14-day regimen. Thus, 10-day therapy may be preferred as first-line treatment in clinical practice.
机译:背景技术伴随着非阶级疗法被推荐为高克拉霉素抵抗区幽门螺杆菌感染的一线治疗,但方案的理想持续时间仍然难以捉摸。本研究的目的是评估10-与14天伴随的H.幽门螺杆菌伴随的疗效和耐受性的疗效和耐受性。方法这是一项前瞻性开放标签的研究,包括未经先前治疗的成年患者的成人患者,没有先前治疗,从2014年9月至2017年6月。伴随的疗法由泮托拉唑40mg,阿莫西林1g,克拉霉素500mg和硝基咪唑500mg组成每日两次在第一阶段施用10天,在研究的第二阶段进行14天。使用Chi-Square和Fisher确切的测试在组之间比较了疗效和副作用。结果,每种协议分析,10-天和14天方案的根除率分别为91.9%(114/124)和90.9%(110/121)(P = 0.77)。有意治疗分析,根除率低于90%。具体而言,10天方案的速率为86.3%(114/132),为14天方案的85.2%(110/129)(p = 0.8)。在31.3%的治疗患者中存在副作用,在14天的组织中明显更常见(P = 0.015)。四名患者停产治疗,所有在14天的群体中。结论十天伴随着H.Pylori的非双产疗法高于14天方案的高度有效和更好的耐受性。因此,在临床实践中,10日治疗可能是优选的作为第一线治疗。

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