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克拉霉素耐药基因型与幽门螺杆菌的根除。

Clarithromycin-resistant genotypes and eradication of Helicobacter pylori.

机构信息

Department of Biomedicina dell'Età Evolutiva, University of Bari, Italy.

出版信息

J Pediatr. 2010 Aug;157(2):228-32. doi: 10.1016/j.jpeds.2010.02.007. Epub 2010 Apr 18.

Abstract

OBJECTIVE

To compare the eradication rates among the different point mutations and the efficacy of triple therapy and a sequential regimen according to genotypic resistance.

STUDY DESIGN

Post hoc retrospective cohort study in a tertiary referral center for pediatric gastroenterology in southern Italy. All 168 children who were positive for Helicobacter pylori were enrolled. Patients had received clarithromycin-based 7-day triple therapy (73 children) or 10-day sequential therapy regimen (95 children). Real-time polymerase chain reaction for assessing clarithromycin resistance was performed on sections of paraffin-embedded gastric biopsy samples.

RESULTS

H pylori eradication was achieved in 16 of 32 (50%) children with the A2143G mutation, in 8 of 10 patients with either A2142G or A2142C strains (80%), and in 112 of 116 children with susceptible strains (88.9%). The presence of A2143G mutation was associated with a lower cure rate compared with the rate in the absence of this mutation (50% vs. 89%; P = .001). The sequential regimen achieved a higher cure rate than triple therapy in patients with A2143G mutant strains (80% vs nil; P < .001).

CONCLUSIONS

The A2143G mutation confers higher risk of treatment failure. Sequential regimen has higher efficacy than standard therapy, even in children with A2143G mutatant strains.

摘要

目的

根据基因型耐药性比较不同点突变的根除率和三联疗法与序贯疗法的疗效。

研究设计

这是意大利南部一家三级儿科胃肠病学转诊中心的事后回顾性队列研究。所有 168 名幽门螺杆菌阳性的儿童均被纳入研究。患者接受了基于克拉霉素的 7 天三联疗法(73 名儿童)或 10 天序贯疗法(95 名儿童)。采用实时聚合酶链反应检测石蜡包埋胃活检样本中克拉霉素的耐药性。

结果

A2143G 突变的 32 名儿童中有 16 名(50%)、A2142G 或 A2142C 菌株的 10 名患者中有 8 名(80%)、敏感株的 116 名儿童中有 112 名(88.9%)根除了幽门螺杆菌。与无此突变相比,A2143G 突变的存在与较低的治愈率相关(50%比 89%;P=.001)。在 A2143G 突变株患者中,序贯疗法的治愈率高于三联疗法(80%比无;P <.001)。

结论

A2143G 突变赋予更高的治疗失败风险。序贯疗法比标准疗法更有效,即使在 A2143G 突变株患儿中也是如此。

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