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Evidence-based medicine: Classifying the evidence from clinical trials – the need to consider other dimensions

机译:循证医学:对临床试验的证据进行分类-需要考虑其他方面

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摘要

The current approach to assessing the quality of evidence obtained from clinical trials focuses on three dimensions: the quality of the design (with double-blinded randomised controlled trials representing the highest level of such design); the statistical power (beta) and the level of significance (alpha). While these aspects are important, we argue that other significant aspects of trial quality impinge upon the truthfulness of the findings: biological plausibility, reproducibility and generalisability. We present several recent studies in critical care medicine where the design, beta and alpha components of the study are seemingly satisfactory but where the aspects of biological plausibility, reproducibility and generalisability show serious limitations. Accordingly, we argue for more reflection, definition and consensus on these aspects of the evaluation of evidence.
机译:当前评估从临床试验获得的证据质量的方法集中在三个方面:设计的质量(双盲随机对照试验代表此类设计的最高水平);统计功效(beta)和显着性水平(alpha)。虽然这些方面很重要,但我们认为试验质量的其他重要方面会影响研究结果的真实性:生物学上的合理性,可重复性和普遍性。我们目前在重症监护医学中进行了几项研究,这些研究的设计,β和α成分看似令人满意,但生物学上的合理性,再现性和通用性方面却显示出严重的局限性。因此,我们主张对证据评估的这些方面进行更多的反思,定义和共识。

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