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布拉氏酵母菌 CNCM I-745 与多菌株芽孢杆菌 clausii 益生菌治疗儿童急性肠胃炎的随机、直接比较研究。

Randomized, direct comparison study of Saccharomyces boulardii CNCM I-745 versus multi-strained Bacillus clausii probiotics for the treatment of pediatric acute gastroenteritis.

机构信息

Consultorio de Pediatria Maza, Buenos Aires, Argentina.

Grupo Pediatrico Belgrano, Buenos Aires, Argentina.

出版信息

Medicine (Baltimore). 2022 Sep 9;101(36):e30500. doi: 10.1097/MD.0000000000030500.

Abstract

BACKGROUND

The choice of an appropriate probiotic for pediatric acute gastroenteritis (PAGE) can be confusing. Our aim was to compare the efficacy and safety of 2 probiotics (Saccharomyces boulardii CNCM I-745 vs a 4-strain mixture of Bacillus clausii O/C, SIN, N/R, T) for the treatment of PAGE.

METHODS

A 2-arm parallel, randomized trial recruited children (6 months to 5 years old) with mild-moderate acute diarrhea, from 8 centers in Argentina. A total of 317 children were enrolled and blindly randomized to 5 days of either S boulardii CNCM I-745 (n = 159) or a 4-strain mixture of B clausii (n = 158), then followed for 7 days post-probiotic treatment. A stool sample was collected at inclusion for pathogen identification. The primary outcome was duration of diarrhea defined as the time from enrollment to the last loose stool followed by the first 24-hour period with stool consistency improvement. Secondary outcomes included frequency of loose stools/day, severity of diarrhea, number reporting no diarrhea at Day 6, time-to-first formed stool, recurrence of diarrhea by study end (Day 12) and safety outcomes.

RESULTS

Three hundred twelve (98%) children completed the study. S boulardii CNCM I-745 showed a significant reduction (P = .04) in the mean duration of diarrhea (64.6 hours, 95% confidence interval [CI] 56.5-72.8) compared to those given B clausii (78.0 hours, 95% CI 69.9-86.1). Both probiotics showed improvement in secondary outcomes and were well-tolerated.

CONCLUSION

In this study, S boulardii CNCM I-745 demonstrated better efficacy than B clausii mix for reducing the duration of pediatric acute diarrhea.

摘要

背景

对于儿科急性肠胃炎(PAGE),选择合适的益生菌可能会令人困惑。我们的目的是比较 2 种益生菌(布拉氏酵母菌 CNCM I-745 与由 4 株芽孢杆菌组成的混合菌,即 B. clausii O/C、SIN、N/R 和 T)治疗 PAGE 的疗效和安全性。

方法

这是一项双臂平行、随机试验,共招募了 8 家阿根廷中心的 317 名 6 个月至 5 岁患有轻度至中度急性腹泻的儿童。所有儿童均接受 5 天的布拉氏酵母菌 CNCM I-745(n=159)或 4 株芽孢杆菌混合菌(n=158)治疗,然后在益生菌治疗后随访 7 天。在纳入时采集粪便样本进行病原体鉴定。主要结局是腹泻持续时间,定义为从入组到最后一次稀便后首次出现 24 小时粪便稠度改善的时间。次要结局包括每日稀便次数、腹泻严重程度、第 6 天无腹泻报告的比例、首次成型粪便的时间、研究结束时(第 12 天)腹泻复发率以及安全性结局。

结果

312 名(98%)儿童完成了研究。与给予 B. clausii 混合菌的儿童相比,布拉氏酵母菌 CNCM I-745 组腹泻持续时间的平均(64.6 小时,95%置信区间[CI] 56.5-72.8)显著缩短(P=0.04)。两种益生菌均改善了次要结局,且耐受性良好。

结论

在这项研究中,与 B. clausii 混合菌相比,布拉氏酵母菌 CNCM I-745 可更有效地缩短儿科急性腹泻的持续时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/526c/9646502/caadd8b93e8b/medi-101-e30500-g001.jpg

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