Seven-day genotypic resistance-guided triple Helicobacter pylori eradication therapy can be highly effective

被引:17
|
作者
Papastergiou, Vasilios [1 ]
Mathou, Nicoletta [1 ]
Licousi, Sophia [2 ]
Evgenidi, Aikaterini [1 ]
Paraskeva, Konstantina D. [1 ]
Giannakopoulos, Athanasios [1 ]
Stavrou, Pinelopi-Zoi [1 ]
Platsouka, Evangelia [2 ]
Karagiannis, John A. [1 ]
机构
[1] Gen Hosp Nea Ionia Konstantopouleio Patission, Dept Gastroenterol, Athens 14223, Greece
[2] Gen Hosp Nea Ionia Konstantopouleio Patission, Dept Microbiol, Athens, Greece
来源
ANNALS OF GASTROENTEROLOGY | 2018年 / 31卷 / 02期
关键词
Helicobacter pylori; tailored therapy; 23SrRNA; gyrA; triple Helicobacter pylori eradication therapy;
D O I
10.20524/aog.2017.0219
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background The efficacy and applicability of molecular testing to guide the selection of antibiotics in triple Helicobacter pylori (H. pylori) eradication regimens have not been reported. We tested a 7-day, genotypic resistance-guided triple H. pylori eradication therapy in a high-resistance setting. Methods Consecutive dyspeptic patients with H. pylori infection were prospectively enrolled. Genotypic resistances to clarithromycin (23SrRNA mutations) and fluoroquinolones (gyrA mutations) were determined from gastric biopsy specimens using a commercially available molecular assay (GenoType(a) HelicoDR). A tailored genotypic resistance-guided 7-day triple therapy comprised esomeprazole, amoxicillin, and either clarithromycin (wild-type 23SrRNA), levofloxacin (23SrRNA mutated/wild-type gyrA) or rifabutin (both 23SrRNA/gyrA mutated). H. pylori eradication was confirmed by C-13-urea breath test. Results Of 148 subjects screened, 51 patients were enrolled (male/female: 27/24, mean age: 50.7 +/- 11.4 years, treatment-naive/-experienced: 32/19). The molecular kit was easily implemented, allowing for rapid (within 24 h) and relatively inexpensive determination of H. pylori resistance (clarithromycin: 47.1%, fluoroquinolones: 15.7%, dual clarithromycin/fluoroquinolones: 7.8%). For patients who received clarithromycin-, levofloxacin-and rifabutin-containing triple therapy, the respective eradication rates were 24/27, 20/20, and 2/4 by intentionto-treat (ITT); and 24/24, 19/19 and 2/3 by per-protocol (PP) analysis. Overall eradication rates were 90.2% (95% confidence interval [CI] 77.8-96.3%) by ITT and 97.8% (95% CI 87-99.8%) by PP analysis, showing no significant difference between treatment-naive and -experienced patients (ITT: 87.5% vs. 94.7%, P=0.64; PP: 96.4% vs. 100%, respectively, P=1.00). Conclusions Regardless of prior treatment history, a genotypic resistance-guided 7-day triple therapy, based on a simple molecular assay, achieved a high H. pylori eradication rate.
引用
收藏
页码:198 / 204
页数:7
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