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双歧杆菌乳亚种补充剂对早产儿的影响:随机对照试验的系统评价。

Effect of Bifidobacterium animalis subsp lactis supplementation in preterm infants: a systematic review of randomized controlled trials.

机构信息

Department of Paediatrics, Medical University of Warsaw, Warsaw, Poland.

出版信息

J Pediatr Gastroenterol Nutr. 2010 Aug;51(2):203-9. doi: 10.1097/MPG.0b013e3181dc0d93.

Abstract

OBJECTIVE

To systematically evaluate and update evidence on the efficacy and safety of Bifidobacterium animalis subsp lactis CNCM I-3446 supplementation in preterm infants.

MATERIALS AND METHODS

The Cochrane Library and MEDLINE databases and major pediatric conference proceedings were searched in December 2008 for randomized controlled trials (RCTs). The company that manufactures B lactis was contacted for unpublished data. The review was restricted to RCTs performed in preterm infants <37 weeks of gestation and/or with a birth weight <2500 g.

RESULTS

Four RCTs involving 324 infants met the inclusion criteria. Compared with controls, B lactis supplementation has the potential to increase fecal bifidobacteria counts and to reduce Enterobacteriaceae and Clostridium spp counts. It also can reduce stool pH and fecal calprotectin concentrations, increase fecal immunoglobulin A and short-chain fatty acid concentrations, and decrease intestinal permeability. Compared with controls, B lactis supplementation had no effect on the risk of necrotizing enterocolitis stage > or = 2 (3 RCTs, n = 293, risk ratio [RR] 0.53, 95% CI 0.16-1.83), risk of sepsis (2 RCTs, 397 cultures, RR 0.6, 95% CI 0.07-5.2), and use of antibiotics (2 RCTs, n = 255, RR 0.67, 95% CI 0.28-1.62). The power of these studies, however, does not allow for a definitive statement regarding a reduced risk of necrotizing enterocolitis. B lactis supplementation did have some effects on anthropometric parameters. No adverse events associated with B lactis supplementation were reported.

CONCLUSIONS

Evidence regarding the potential beneficial effects of B lactis supplementation in preterm infants is encouraging. Further studies to assess clinically relevant outcomes are needed.

摘要

目的

系统评价和更新双歧杆菌乳亚种 CNCM I-3446 补充剂对早产儿的疗效和安全性的证据。

材料与方法

检索 2008 年 12 月 Cochrane 图书馆、MEDLINE 数据库和主要儿科会议记录,寻找随机对照试验(RCT)。与生产 B 乳杆菌的公司联系,以获取未发表的数据。该综述仅限于在妊娠<37 周和/或出生体重<2500 g 的早产儿中进行的 RCT。

结果

符合纳入标准的 4 项 RCT 共纳入 324 名婴儿。与对照组相比,B 乳杆菌补充剂有可能增加粪便双歧杆菌计数,减少肠杆菌科和梭菌属计数。它还可以降低粪便 pH 值和粪便钙卫蛋白浓度,增加粪便免疫球蛋白 A 和短链脂肪酸浓度,并降低肠道通透性。与对照组相比,B 乳杆菌补充剂对坏死性小肠结肠炎程度>或=2 的风险(3 项 RCT,n=293,风险比[RR]0.53,95%CI 0.16-1.83)、败血症的风险(2 项 RCT,397 个培养物,RR 0.6,95%CI 0.07-5.2)和抗生素的使用(2 项 RCT,n=255,RR 0.67,95%CI 0.28-1.62)均无影响。然而,这些研究的效力不允许对坏死性小肠结肠炎风险降低做出明确的陈述。B 乳杆菌补充剂对人体测量参数有一定影响。未报告与 B 乳杆菌补充剂相关的不良反应。

结论

关于 B 乳杆菌补充剂对早产儿潜在有益作用的证据令人鼓舞。需要进一步研究以评估临床相关结局。

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