首页> 外文期刊>The Journal of Antimicrobial Chemotherapy >Profound effect of study design factors on ventilator-associated pneumonia incidence of prevention studies: benchmarking the literature experience.
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Profound effect of study design factors on ventilator-associated pneumonia incidence of prevention studies: benchmarking the literature experience.

机译:研究设计因素对呼吸机相关性肺炎预防研究的深远影响:以文献经验为基准。

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BACKGROUND: The ventilator-associated pneumonia incident proportion (VAP-IP) is highly variable among control groups of studies of methods for its prevention. The objective here is to develop and validate a literature-derived benchmark against which these groups can be profiled. METHODS: A literature search yielded 95 cohort groups and control and intervention groups of 150 studies of either non-antimicrobial or antimicrobial methods of VAP prevention. The 95 cohort groups comprise a benchmark set (30 groups), from which the reference funnel plot (RFP) was derived, and a search set (65 groups), against which the benchmark was validated. The VAP-IP data of the benchmark set were found in five published systematic reviews, whereas the VAP-IP data of the search set were abstracted directly from the literature. FINDINGS: Among the 95 cohort groups, the VAP-IP of groups with size >399 was significantly lower than the VAP-IP of smaller groups. Compared with the RFP, 15 of 51 (29%) control groups from studiesof antimicrobial methods of VAP prevention with concurrent design were high outlier versus 2 of 110 (2%) control groups from other types of study design (P < 0.001). There were only 22 (14%) outlier groups, all low outlier, among the 162 intervention groups. CONCLUSIONS: Study design factors such as concurrency and study size have potentially greater influence on the VAP-IP than do the VAP prevention methods under study. The outlier status of control groups were inapparent in the individual studies and the meta-analyses and yet would have confounded the estimates of treatment effect.
机译:背景:呼吸机相关性肺炎的发病率(VAP-IP)在控制其方法的对照组中差异很大。此处的目的是开发和验证源自文献的基准,可以对这些基准进行分析。方法:文献检索产生了95个队列组,对照组和干预组进行了150项关于VAP预防的非抗菌或抗菌方法的研究。这95个队列组包括一个基准集(30个组)和一个搜索集(65个组),从基准集中可以得出参考漏斗图(RFP),基准可以用来验证基准。在五个已发表的系统评价中找到了基准集的VAP-IP数据,而直接从文献中提取了搜索集的VAP-IP数据。结果:在95个队列组中,规模大于399的组的VAP-IP显着低于较小组的VAP-IP。与RFP相比,采用抗菌VAP预防方法并发设计的对照组中有15个(29%)对照组有较高的异常值,而其他类型的研究设计中有110个(2%​​)对照组中有2个(P <0.001)。在162个干预组中,只有22个(14%)异常值组,所有异常值较低。结论:研究设计因素,如并发性和研究规模,对VAP-IP的影响可能比所研究的VAP预防方法更大。对照组的异常状态在个别研究和荟萃分析中不明显,但可能会混淆治疗效果的估计。

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