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首页> 外文期刊>Parasitology Research >Clinical efficacy of Saccharomyces boulardii or metronidazole in symptomatic children with Blastocystis hominis infection
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Clinical efficacy of Saccharomyces boulardii or metronidazole in symptomatic children with Blastocystis hominis infection

机译:博拉氏酵母菌或甲硝唑治疗有症状儿童人型芽孢杆菌感染的临床疗效

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Although many Blastocystis infections remain asymptomatic, recent data suggest it also causes frequent symptoms. Therapy should be limited to patients with persistent symptoms and a complete workup for alternative etiologies. The goal of this study was to compare the natural evolution (no treatment) to the efficacy of Saccharomyces boulardii (S. boulardii) or metronidazole for the duration of diarrhea and the duration of colonization in children with gastrointestinal symptoms and positive stool examination for Blastocystis hominis. This randomized single-blinded clinical trial included children presenting with gastrointestinal symptoms (abdominal pain, diarrhea, nausea–vomiting, flatulence) more than 2 weeks and confirmed B. hominis by stool examination (B. hominis cysts in the stool with microscopic examination of the fresh stool). The primary end points were clinical evaluation and result of microscopic stool examination at day 15. Secondary end points were the same end points at day 30. Randomization was performed by alternating inclusion: group A, S. boulardii (250 mg twice a day, Reflor®) during 10 days; group B, metronidazole (30 mg/kg twice daily) for 10 days; group C, no treatment. At day 15 and 30 after inclusion, the patients were re-evaluated, and stool samples were examined microscopically. On day 15, children that were still symptomatic and/or were still B. hominis-infected in group C were treated with metronidazole for 10 days. There was no statistically significant difference between the three study groups for age, gender, and the presence of diarrhea and abdominal pain. On day 15, clinical cure was observed in 77.7% in group A (n, 18); in 66.6% in group B (n, 15); and 40% in group C (n:15) (p < 0.031, between groups A and C). Disappearance of the cysts from the stools on day 15 was 80% in group B, 72.2% in group A, and 26.6% in group C (p = 0.011, between group B and group C; p = 0.013, between group A and group C). At the end of the first month after inclusion, clinical cure rate was 94.4% in group A and 73.3% in group B (p = 0.11). Parasitological cure rate for B. hominis was very comparable between both groups (94.4% vs. 93.3%, p = 0.43). Metronidazole or S. boulardii has potential beneficial effects in B. hominis infection (symptoms, presence of parasites). These findings challenge the actual guidelines.
机译:尽管许多芽孢杆菌感染仍无症状,但最近的数据表明它也引起频繁的症状。治疗应仅限于具有持续性症状且对其他病因进行完整检查的患者。这项研究的目的是比较自然进化(无治疗)与博拉氏糖酵母(S. boulardii)或甲硝唑对腹泻持续时间和胃肠道症状患儿定植持续时间以及人乳芽孢杆菌粪便检查阳性的儿童的疗效。 。这项随机单盲临床试验包括表现出胃肠道症状(腹痛,腹泻,恶心呕吐,肠胃气胀)超过2周的儿童,并通过粪便检查证实了人型芽孢杆菌(B. hominis囊肿,并通过显微镜检查了粪便)。新鲜的大便)。主要终点为临床评估和第15天的粪便显微检查结果。次要终点为第30天的相同终点。通过交替纳入进行随机分组:A组,S. boulardii(250 mg,每天两次,Reflor) ®)在10天内; B组甲硝唑(30 mg / kg每天两次),持续10天; C组,无治疗。入院后第15天和第30天,对患者进行重新评估,并对粪便样本进行显微镜检查。在第15天,用甲硝唑治疗在C组中仍然有症状和/或仍感染人双歧杆菌的儿童10天。三个年龄,性别,腹泻和腹痛的存在之间在三个研究组之间没有统计学上的显着差异。在第15天,A组的临床治愈率为77.7%(n,18); B组中66.6%(n,15);在C组中占40%(n:15)(A和C组之间p <0.031)。 B组第15天粪便中的囊肿消失率为80%,A组为72.2%,C组为26.6%(B组与C组之间为p = 0.011; A组与C组之间为p = 0.013) C)。入选后第一个月末,A组和B组的临床治愈率分别为94.4%和73.3%(p = 0.11)。两组间人双歧杆菌的寄生虫治愈率非常相似(94.4%对93.3%,p = 0.43)。甲硝唑或S. boulardii对人型芽孢杆菌感染(症状,寄生虫的存在)具有潜在的有益作用。这些发现挑战了实际准则。

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