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兰索拉唑、克拉霉素和阿莫西林三联疗法对根除幽门螺杆菌阳性功能性(非溃疡性)消化不良无明显症状改善作用。

Absence of symptomatic benefit of lansoprazole, clarithromycin, and amoxicillin triple therapy in eradication of Helicobacter pylori positive, functional (nonulcer) dyspepsia.

作者信息

Veldhuyzen van Zanten Sander, Fedorak Richard N, Lambert Jean, Cohen Lawrence, Vanjaka Anita

机构信息

Division of Gastroenterology, Department of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Am J Gastroenterol. 2003 Sep;98(9):1963-9. doi: 10.1111/j.1572-0241.2003.07583.x.

Abstract

OBJECTIVES

The aim of this study was to compare the effect of a combination of lansoprazole, clarithromycin, and amoxicillin (LCA) versus placebo on the severity of symptoms in functional dyspepsia patients who were positive for Helicobacter pylori (H. pylori).

METHODS

This was a double-blind, randomized, controlled clinical trial in adult patients with functional dyspepsia who were H. pylori positive. Patients were randomized to 7-day treatment with LCA or identical looking placebo. H. pylori status was confirmed by the urea breath test performed at baseline, at 6 wk, and at 6 and 12 months. The severity of eight upper GI symptoms was measured on a five-point Likert scale. The main outcomes were the change in average severity of the dyspepsia summary score of the eight symptoms and the proportion of patients who improved >/=4 points on the dyspepsia summary score.

RESULTS

A total of 157 patients were included in the intention-to-treat analysis. LCA achieved cure of H. pylori infection in 82% of patients compared to 6% in the placebo group. The severity of dyspepsia symptoms improved over the 12-month study period, but for none of the outcome measures was there a significant difference between LCA and placebo.

CONCLUSIONS

There was no difference in sustained improvement of dyspepsia symptoms when LCA was compared with placebo. An 82% cure rate of H. pylori infection was observed with LAC.

摘要

目的

本研究旨在比较兰索拉唑、克拉霉素和阿莫西林联合用药(LCA)与安慰剂对幽门螺杆菌(H. pylori)阳性的功能性消化不良患者症状严重程度的影响。

方法

这是一项针对H. pylori阳性的成年功能性消化不良患者的双盲、随机、对照临床试验。患者被随机分为接受LCA治疗7天或外观相同的安慰剂治疗。通过在基线、6周、6个月和12个月时进行的尿素呼气试验确认H. pylori状态。采用五点李克特量表测量八种上消化道症状的严重程度。主要结局指标为八种症状的消化不良综合评分平均严重程度的变化以及消化不良综合评分提高≥4分的患者比例。

结果

共有157例患者纳入意向性分析。LCA使82%的患者幽门螺杆菌感染得到治愈,而安慰剂组为6%。在12个月的研究期间,消化不良症状的严重程度有所改善,但在任何结局指标上,LCA与安慰剂之间均无显著差异。

结论

LCA与安慰剂相比,在消化不良症状的持续改善方面没有差异。LAC观察到幽门螺杆菌感染治愈率为82%。

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