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基于莫西沙星-右旋兰索拉唑的7天和14天三联疗法及益生菌补充剂根除泰国非溃疡性消化不良患者幽门螺杆菌的疗效:一项双盲随机安慰剂对照研究

Effectiveness of 7-Day and 14-Day Moxifloxacin-Dexlansoprazole Based Triple Therapy and Probiotic Supplement for Helicobacter Pylori Eradication in Thai Patients with Non-Ulcer Dyspepsia: A Double-Blind Randomized Placebo-Controlled Study.

作者信息

Chotivitayatarakorn Peranart, Mahachai Varocha, Vilaichone Ratha-Korn

机构信息

Gastroenterology Unit, Thammasat University Hospital, Pathumthani,, Thailand.

National Gastric Cancer and Gastrointestinal diseases Research Center, Bangkok, Thailand. Email:

出版信息

Asian Pac J Cancer Prev. 2017 Oct 26;18(10):2839-2843. doi: 10.22034/APJCP.2017.18.10.2839.

Abstract

Background: Helicobacter pylori (H. pylori) is important cause of peptic ulcer and gastric cancer. Moxifloxacin is effective antibiotic for treatment for H. pylori. However, there were limited studies as first line therapy. Probiotics had been shown to decrease therapy-related side-effect and increase eradication rate. Aim of this study was to evaluate the efficacy of moxifloxacin-dexlansoprazole based triple therapy with probiotic for H. pylori treatment in Thailand. Methods: Patients with H. pylori infected gastritis were randomized to receive 7- or 14-day moxifloxacin-dexlansoprazole based triple therapy with probiotic or placebo. Regimen consisted of 60 mg dexlansoprazole twice daily, 400mg moxifloxacin once daily, 1g clarithromycin MR once daily. Probiotic used in this study was 282.5mg Saccharomyces boulardii (S. boulardii) in capsule prescribed twice daily. CYP2C19 genotyping, antibiotic susceptibility tests, and CagA genotyping were also done. Successful eradication was defined as a negative 13C-urea breath test at least 4 weeks after treatment. Results: Total of 108 subjects was enrolled (27 each to 7-and 14-day regimens with probiotic or placebo). Antibiotic susceptibility tests showed 29% fluoroquinolone, 19% metronidazole and 4% clarithromycin resistance. CYP2C19 genotyping demonstrated 43%, 47% and 11% were rapid, intermediate and poor metabolizers, respectively. CagA genes were positive in all patients. Eradication rates of 7-day and 14-day regimens with probiotic were 100%, and 93% respectively. There were no significant differences between eradication rate of 7-day and 14-day regimen with or without probiotics. Regarding side-effects, incidence of nausea, abdominal discomfort, bitter taste, and diarrhea were significantly lower in regimen with probiotic group compared with placebo(7.4%vs. 22.2%; p=0.028, 0.00%vs.14.8%; p=0.003, 35.2%vs.70.4%; p=0.0002, and 0.00%vs.9.3%; p=0.028, respectively). Conclusions: 7-day moxifloxacindexlansoprazole therapy plus S. boulardii provide an reliable cure rate of H. pylori in non-ulcer dyspeptic patients in Thailand, independent of CYP2C19 genotype. Probiotic adding also decreased side effects during the treatment.

摘要

背景

幽门螺杆菌(H. pylori)是消化性溃疡和胃癌的重要病因。莫西沙星是治疗幽门螺杆菌的有效抗生素。然而,作为一线治疗的研究有限。益生菌已被证明可减少治疗相关副作用并提高根除率。本研究的目的是评估在泰国使用基于莫西沙星 - 右兰索拉唑的三联疗法加益生菌治疗幽门螺杆菌的疗效。方法:幽门螺杆菌感染性胃炎患者被随机分为接受7天或14天基于莫西沙星 - 右兰索拉唑的三联疗法加益生菌或安慰剂。治疗方案包括每日两次60毫克右兰索拉唑、每日一次400毫克莫西沙星、每日一次1克克拉霉素缓释片。本研究中使用的益生菌是胶囊装的282.5毫克布拉氏酵母菌(S. boulardii),每日服用两次。还进行了CYP2C19基因分型、抗生素敏感性测试和CagA基因分型。成功根除定义为治疗后至少4周13C - 尿素呼气试验阴性。结果:共纳入108名受试者(益生菌或安慰剂组各27名接受7天和14天治疗方案)。抗生素敏感性测试显示氟喹诺酮耐药率为29%,甲硝唑为19%,克拉霉素为4%。CYP2C19基因分型显示快速代谢者、中间代谢者和慢代谢者分别为43%、47%和11%。所有患者CagA基因均为阳性。含益生菌的7天和14天治疗方案的根除率分别为100%和93%。含或不含益生菌的7天和14天治疗方案的根除率之间无显著差异。关于副作用,益生菌组恶心、腹部不适、口苦和腹泻的发生率明显低于安慰剂组(分别为7.4%对22.2%;p = 0.028,0.00%对14.8%;p = 0.003,35.2%对70.4%;p = 0.0002,0.00%对9.3%;p = 0.028)。结论:在泰国,7天莫西沙星 - 右兰索拉唑疗法加布拉氏酵母菌可为非溃疡性消化不良患者提供可靠的幽门螺杆菌治愈率,与CYP2C19基因型无关。添加益生菌还可减少治疗期间的副作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/487a/5747412/ae40053a4363/APJCP-18-2839-g001.jpg

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