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结构方程模型作为一种概念验证工具,用于研究重症监护病房患者局部抗生素预防与六种血流感染类型之间的中介机制。

Structural Equation Modelling as a Proof-of-Concept Tool for Mediation Mechanisms Between Topical Antibiotic Prophylaxis and Six Types of Blood Stream Infection Among ICU Patients.

作者信息

Hurley James

机构信息

Melbourne Medical School, University of Melbourne, Parkville, VIC 3052, Australia.

Ballarat Health Services, Grampians Health, Ballarat, VIC 3350, Australia.

出版信息

Antibiotics (Basel). 2024 Nov 18;13(11):1096. doi: 10.3390/antibiotics13111096.

DOI:10.3390/antibiotics13111096
PMID:39596789
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11591272/
Abstract

Whether exposing the microbiome to antibiotics decreases or increases the risk of blood stream infection with , , , and among ICU patients, and how this altered risk might be mediated, are critical research questions. Addressing these questions through the direct study of specific constituents within the microbiome would be difficult. An alternative tool for addressing these research questions is structural equation modelling (SEM). SEM enables competing theoretical causation networks to be tested 'en bloc' by confrontation with data derived from the literature. These causation models have three conceptual steps: exposure to specific antimicrobials are the key drivers, clinically relevant infection end points are the measurable observables, and the activity of key microbiome constituents on microbial invasion serve as mediators. These mediators, whether serving to promote, to impede, or neither, are typically unobservable and appear as latent variables in each model. SEM methods enable comparisons through confronting the three competing models, each versus clinically derived data with the various exposures, such as topical or parenteral antibiotic prophylaxis, factorized in each model. colonization, represented as a latent variable, and concurrency are consistent promoters of all types of blood stream infection, and emerge as harmful mediators.

摘要

使微生物群暴露于抗生素是会降低还是增加重症监护病房(ICU)患者发生由[具体细菌名称1]、[具体细菌名称2]、[具体细菌名称3]和[具体细菌名称4]引起的血流感染的风险,以及这种改变后的风险可能如何介导,是关键的研究问题。通过直接研究微生物群中的特定成分来解决这些问题将很困难。解决这些研究问题的另一种工具是结构方程模型(SEM)。SEM能够通过与来自文献的数据进行对比,对相互竞争的理论因果网络进行“整体”检验。这些因果模型有三个概念步骤:暴露于特定抗菌药物是关键驱动因素,临床相关的感染终点是可测量的可观测变量,关键微生物群成分对微生物入侵的作用作为中介变量。这些中介变量,无论是起到促进、阻碍作用,还是两者都不起作用,通常都是不可观测的,并且在每个模型中都表现为潜在变量。SEM方法通过对比三种相互竞争的模型来进行比较,每种模型都与临床得出的数据进行对比,其中每种模型都对各种暴露因素进行了分解,如局部或胃肠外抗生素预防。[具体细菌名称]的定植作为一个潜在变量,并且并发感染是所有类型血流感染的一致促进因素,并作为有害的中介变量出现。

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引用本文的文献

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