Combination of gastroprotectors and probiotics in the eradication of H. pylori infection: results of a randomized comparative clinical trial

A.A. Tryapyshko, Natalya N. Dekhnich
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Abstract

Objective. To compare efficacy and safety of 14-day triple eradication therapy with the addition of methylmethionine sulfonium chloride and a probiotic complex and 14-day triple eradication therapy boosted with bismuth tripotassium dicitrate and a probiotic complex in a prospective comparative randomized clinical trial. Materials and Methods. A total of 70 patients with confirmed H. pylori infection were enrolled into the study. The first group (n = 35) received esomeprazole 20 mg 2 bid, clarithromycin 500 mg bid and amoxicillin 1000 mg bid for 14 days, methylmethionine sulfonium chloride 300 mg once a day for 1 month, probiotic complex (bifidobacteria [Bifidobacterium longum CBT BG7, Bifidobacterium lactis CBT BL3, Bifidobacterium bifidum CBT BF3], lactobacilli [Lactobacillus acidophilus CBT LA1, Lactobacillus rhamnosus CBT LR5], Streptococcus thermophilus CBT ST3) 1 capsule once a day for 1 month. The second group (n = 35) received esomeprazole 20 mg 2 bid, clarithromycin 500 mg 2 bid, amoxicillin 1000 mg 2 bid and bismuth tripotassium dicitrate 240 mg 2 bid for 14 days, probiotic complex (bifidobacteria [Bifidobacterium longum CBT BG7, Bifidobacterium lactis CBT BL3, Bifidobacterium bifidum CBT BF3], lactobacilli [Lactobacillus acidophilus CBT LA1, Lactobacillus rhamnosus CBT LR5], Streptococcus thermophilus CBT ST3) 1 capsule once a day for 1 month. Eradication of H. pylori was assessed using stool antigen test. Results. Eradication rates for the first and second groups in the intent-to-treat (ITT) population were 77.1% and 88.6% (p = 0.205), respectively. In the per-protocol (PP) population, eradication rates were 81.8% and 96.9% (p = 0.051), respectively. Adverse events were reported in 34.3% of patients in the first group and 34.3% of patients in the second group (p = 1). Conclusions. 14-day standard triple therapy boosted with bismuth tripotassium dicitrate and a probiotic complex demonstrates high efficacy and safety profile, and therefore can be recommended as first-line therapy for H. pylori infection in adults.
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胃保护剂和益生菌联合用于根除幽门螺杆菌感染:一项随机对照临床试验的结果
目标。在一项前瞻性比较随机临床试验中,比较添加甲基蛋氨酸磺酸和益生菌复合物的14天三联根除治疗和添加三硝酸二钾铋和益生菌复合物的14天三联根除治疗的疗效和安全性。材料与方法。共有70名确诊幽门螺杆菌感染的患者参加了这项研究。第一组(n = 35)唑收到20 mg 2报价,克拉霉素500毫克出价和阿莫西林1000毫克申请14天,methylmethionine锍氯化1个月每天300毫克一次,益生菌复杂(双歧杆菌(双歧杆菌longum CBT BG7,双歧杆菌lactis CBT b13,双歧杆菌bifidum CBT BF3),乳酸杆菌(嗜酸乳杆菌CBT LA1,乳杆菌CBT LR5),乳酸链球菌CBT ST3) 1胶囊每天一次为1个月。第二组(n = 35)给予埃索美拉唑20 mg 2 bid,克拉霉素500 mg 2 bid,阿莫西林1000 mg 2 bid,二硝酸铋三钾240 mg 2 bid,连用14天,益生菌复合物(双歧杆菌[长双歧杆菌CBT BG7,乳酸双歧杆菌CBT BL3,两歧双歧杆菌CBT BF3],乳酸菌[嗜酸乳杆菌CBT LA1,鼠李糖乳杆菌CBT LR5],嗜热链球菌CBT ST3) 1粒胶囊,每天1次,连用1个月。采用粪便抗原试验评估幽门螺杆菌根除情况。结果。意向治疗人群中第一组和第二组的根除率分别为77.1%和88.6% (p = 0.205)。在按方案(PP)群体中,根除率分别为81.8%和96.9% (p = 0.051)。第一组和第二组分别有34.3%和34.3%的患者报告了不良事件(p = 1)。结论:14天标准三联疗法以三硝酸铋和益生菌复合物为基础,具有较高的疗效和安全性,因此可以推荐作为成人幽门螺杆菌感染的一线治疗。
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8 weeks
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