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Manipulation of the microbiome in critical illness—probiotics as a preventive measure against ventilator-associated pneumonia

机译:危急疾病中微生物组的操作—益生菌作为预防呼吸机相关性肺炎的措施

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ObjectiveTo describe the possible modes of action of probiotics and provide a systematic review of the current evidence on the efficacy of probiotics to prevent ventilator-associated pneumonia (VAP) in critically ill patients. MethodsWe conducted an unrestricted search of the English language medical literature. For each individual study, the relative risk of VAP was calculated using the reported primary outcome data. ResultsThe search identified a total of 72 articles. Eight articles enrolling a total of 1229 patients fulfilled the inclusion and exclusion criteria. In four trials, the investigators were blinded for the intervention, and two trials used an intention-to-treat analysis. Loss to follow-up with regard to the primary endpoint ranged from 0 to 14% in the intervention groups and from 0 to 16% in the control groups. The incidence of VAP expressed as the percentage of studied patients was reported in seven trials. The incidence of VAP ranged from 4 to 36% in the intervention groups and from 13 to 50% in the control groups. The relative risk for VAP ranged between 0.30 and 1.41. Three trials showed a significant difference in favor of probiotic therapy between the intervention and the control groups. ConclusionsThe incidence of VAP tended to be lower in patients treated with probiotics in most trials identified by the systematic search. Due to the heterogeneity of the studies and the low quality of evidence, it remains difficult to draw firm conclusions. The efficacy of preventive probiotics should be studied in more detail in future trials. Application of probiotics for the prevention of VAP seems to be safe with only few side effects reported in the selected trials.
机译:目的描述益生菌可能的作用方式,并就益生菌预防危重患者呼吸机相关肺炎(VAP)的功效的现有证据进行系统综述。方法我们对英语医学文献进行了无限制的检索。对于每个单独的研究,使用报告的主要结果数据计算VAP的相对风险。结果搜索共找到72篇文章。总共纳入1229名患者的八篇文章符合纳入和排除标准。在四项试验中,研究人员对干预视而不见,而两项试验使用了意向性治疗分析。在主要终点方面,干预组的随访损失范围为0%至14%,对照组为0%至16%。在七项试验中报告了以研究患者百分比表示的VAP发生率。 VAP的发生率在干预组中为4%至36%,在对照组中为13%至50%。 VAP的相对风险介于0.30和1.41之间。三项试验显示干预组和对照组在支持益生菌治疗方面存在显着差异。结论在通过系统搜索确定的大多数试验中,用益生菌治疗的患者中VAP的发生率往往较低。由于研究的异质性和证据质量低下,仍然很难得出明确的结论。预防性益生菌的功效应在以后的试验中进行更详细的研究。益生菌用于预防VAP似乎是安全的,在所选试验中报道的副作用很少。

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