期刊
HELICOBACTER
卷 18, 期 4, 页码 270-273出版社
WILEY-BLACKWELL
DOI: 10.1111/hel.12041
关键词
amoxicillin; Helicobacter pylori; Improved triple therapy; clarithromycin; nonulcer dyspepsia; proton pump inhibitors; Thailand
资金
- Faculty of Medicine, Thammasat University Hospital, Thailand
- Gastroenterology Association of Thailand (GAT)
- National Research University Project of Thailand Office of Higher Education Commission
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 (60mg) twice daily, amoxicillin 1g twice daily, and long-acting clarithromycin MR 1g 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 13C-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 14days 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.
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