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The case-case-control study design: addressing the limitations of risk factor studies for antimicrobial resistance.

机译:病例-病例-对照研究设计:解决抗菌素耐药性危险因素研究的局限性。

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OBJECTIVE: There are significant limitations of the standard case-control study design for identifying risk factors for resistant organisms. The objective of this study was to develop a study design to overcome these limitations. DESIGN: Theoretical analysis of different types of study designs that can be used in risk factor studies for resistant organisms. RESULTS: We developed the case-case-control study design, which uses two separate case-control analyses within a single study. The first analysis compares patients infected with resistant bacteria (resistant cases) with control-patients without infection caused by the target organism, who are therefore representative of the source population; and the second analysis compares patients infected with the susceptible phenotype of the target organism (susceptible cases) with the same control-patients without infection caused by the target organism. These two analyses provide risk models for (1) isolation of the resistant phenotype of the target organism as compared with the source population and (2) isolation of the susceptible phenotype of the organism as compared with the source population. When these two risk models are compared and contrasted, risk factors specifically associated with isolation of the resistant phenotype can be identified. CONCLUSIONS: The case-case-control study design is an effective method for identifying risk factors for antimicrobial-resistant pathogens. Although the case-case-control study design has limitations, it is, in our opinion, more informative and less flawed than the standard case-control study design.
机译:目的:标准病例对照研究设计在识别耐药菌危险因素方面存在明显局限性。这项研究的目的是开发一种克服这些局限性的研究设计。设计:可用于耐药菌风险因素研究的不同类型研究设计的理论分析。结果:我们开发了病例-病例对照研究设计,该研究设计在单个研究中使用了两个单独的病例对照分析。第一个分析将感染抗药性细菌的患者(抗药性病例)与没有由目标生物体引起感染的对照患者进行比较,这些患者因此可以代表来源人群;第二种分析将感染目标生物的易感表型的患者(易感病例)与没有感染目标生物的对照患者进行比较。这两种分析提供了以下风险模型:(1)与来源种群相比,分离目标生物的抗性表型;(2)与来源种群相比,分离目标生物的易感表型。通过比较和对比这两种风险模型,可以确定与抗性表型分离特别相关的风险因素。结论:病例-病例-对照研究设计是确定抗药性耐药病原体危险因素的有效方法。尽管案例-病例对照研究设计有局限性,但在我们看来,它比标准病例-对照研究设计具有更多的信息和更少的缺陷。

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