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Clinical study on saccharomyces boulardii in the treatment of patients with mild to moderate ulcerative colitis

机译:Saccharomyces Boulardii治疗轻度至中度溃疡性结肠炎患者的临床研究

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Aim: To investigate the clinical therapeutic efficacy of saccharomyces boulardii(Sb) in combination with mesalazine in patients with mild to moderate ulcerative colitis (UC). Methods: Sixty patients aged 18 to 75 years with mild to moderate UC were divided into two groups, the combination group and the mesalazine group. Clinical remission rate (CRR) was calculated with the formula: CRR= number of complete remission cases + number of effective cases)/all cases. The clinical symptom score (CSS), endoscopic score (ES) and histopathological score (HS) were recorded before and after treatment. Result: After two week's treatment, the CSS in the combination group was significantly decreased (P0.05), but in the mesalazine group it showed no significant changes (P>0.05). After four week's treatment, the CSS in both combination group and mesalazine group was significantly decreased(P0.05). After 8 week's treatment, the CSS, ES and HS in the combination group were significantly lower than those in the mesalazine group(P0.05). CRR in the combination group (46.7%) was significantly higher than that in the mesalazine group (20.0%) after 8 weeks' treatment (P0.05). Conclusion: Saccharomyces boulardii in combination with mesalazine is faster and more effective in improving clinical symptoms, endoscopic and histopathological changes in patients with mild to moderate UC than using mesalazine alone.
机译:目的:探讨Saccharomyces Boulardii(Sb)与Messalazine在轻度至中度溃疡性结肠炎(UC)的患者中的临床治疗疗效。方法:60岁患者18至75岁,轻度至中度UC患者分为两组,组合组和咪纳碱基。用公式计算临床缓解率(CRR):CRR =完全缓解案件的数量+有效案件的数量)/所有情况。在治疗之前和之后记录临床症状评分(CSS),内镜分数(ES)和组织病理分数(HS)。结果:经过两周的治疗后,组合组中的CSS显着降低(P <0.05),但在甲烷嗪组中,它显示出没有显着的变化(P> 0.05)。在四周的治疗后,组合组和胚轴组的CSS显着降低(P <0.05)。在8周的治疗后,组合组中的CSS,ES和HS显着低于中甲胺基团中的CSS,ES和HS(P <0.05)。组合组(46.7%)的CRR显着高于Mesalazine Group(20.0%)治疗后(P <0.05)。结论:Boulomyces Boulardii与Mesalazine组合的速度更快,更有效地改善轻度至中等UC患者的临床症状,内镜和组织病理学变化而不是单独使用甲烷嗪。

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