首页> 外文期刊>Helicobacter >Improved Efficacy of Proton Pump Inhibitor - Amoxicillin - Clarithromycin Triple Therapy for Helicobacter pylori Eradication in Low Clarithromycin Resistance Areas or for Tailored Therapy
【24h】

Improved Efficacy of Proton Pump Inhibitor - Amoxicillin - Clarithromycin Triple Therapy for Helicobacter pylori Eradication in Low Clarithromycin Resistance Areas or for Tailored Therapy

机译:改善质子泵抑制剂-阿莫西林-克拉霉素三联疗法在低克拉霉素耐药性地区根除幽门螺杆菌的效果或量身定制的疗法

获取原文
获取原文并翻译 | 示例
           

摘要

Objective: Standard triple therapy for Helicobacter pylori eradication is no longer effective as an empiric choice in most areas. Even in low clarithromycin resistance areas, results ≥95% are infrequently achieved. This study was designed to search for a version of standard triple therapy for use low prevalence areas or as tailored therapy that is highly effective irrespective of CYP2C19 genotype. Design: Two prospective pilot single center studies were performed in Thailand. H. pylori-infected subjects were randomized to 7- or 14-day regimens using a high-dose proton pump inhibitor (PPI) triple therapy consisting of lansoprazole (60 mg) twice daily, amoxicillin 1 g twice daily, and long-acting clarithromycin MR 1 g once daily. H. pylori was defined as positive H. pylori culture; or two positive tests (rapid urease test and histology); CYP2C19 genotyping was performed. H. pylori eradication was evaluated by ~(13)C-UBT 4 or more weeks after treatment. Results: Hundred and ten subjects were enrolled (55 each to the 7- and 14-day regimens). Antibiotic susceptibility testing (25 strains) showed 40% metronidazole resistance but no clarithromycin resistance. CYP2C19 genotyping (64 subjects) revealed 56.3% rapid metabolizer, 29.7% intermediate metabolizer, and 14% poor metabolizer. The eradication rate with the 14-day regimen was 100% (95% CI = 93.5-100%) and 92.7% (95% CI = 82-97%) with the 7-day regimen. The difference was related to improved eradication at 14 days in rapid metabolizers (i.e. 100 vs 88.2%). Conclusion: Triple therapy using a 14-day high-dose PPI and long-acting clarithromycin provided an excellent cure rate (100%) regardless of the CYP2C19 genotype.
机译:目的:根除幽门螺杆菌的标准三联疗法在大多数地区不再是有效的经验选择。即使在克拉霉素耐药性较低的地区,也很少能达到≥95%的结果。本研究旨在寻找低流行区域的标准三联疗法的一种版本,或作为高效疗法的量身定制疗法,与CYP2C19基因型无关。设计:在泰国进行了两项前瞻性试点单中心研究。使用高剂量质子泵抑制剂(PPI)三联疗法将幽门螺杆菌感染的受试者随机分为7天或14天方案,三联疗法由兰索拉唑(60 mg)每天两次,阿莫西林1 g每天两次和长效克拉霉素组成每天MR 1克。幽门螺杆菌被定义为阳性幽门螺杆菌培养;或两个阳性测试(快速尿素酶测试和组织学);进行CYP2C19基因分型。在治疗后4周或更长时间通过〜(13)C-UBT评估幽门螺杆菌的根除情况。结果:招募了一百十名受试者(7天和14天治疗方案各55名)。抗生素药敏试验(25个菌株)显示出40%的甲硝唑耐药性,而克拉霉素没有耐药性。 CYP2C19基因分型(64名受试者)显示快速代谢者为56.3%,中间代谢者为29.7%,不良代谢者为14%。 14天治疗方案的根除率为100%(95%CI = 93.5-100%),而7天治疗方案的根除率为92.7%(95%CI = 82-97%)。差异与快速代谢者在14天时的根除改善有关(即100对88.2%)。结论:不论CYP2C19基因型如何,使用14天大剂量PPI和长效克拉霉素的三联疗法均可提供出色的治愈率(100%)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号