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在实验室实验中随着数据积累进行的中期分析。

Interim analyses of data as they accumulate in laboratory experimentation.

作者信息

Ludbrook John

机构信息

Department of Surgery, The University of Melbourne, Parkville, Victoria, Australia.

出版信息

BMC Med Res Methodol. 2003 Aug 21;3:15. doi: 10.1186/1471-2288-3-15.

Abstract

BACKGROUND

Techniques for interim analysis, the statistical analysis of results while they are still accumulating, are highly-developed in the setting of clinical trials. But in the setting of laboratory experiments such analyses are usually conducted secretly and with no provisions for the necessary adjustments of the Type I error-rate.

DISCUSSION

Laboratory researchers, from ignorance or by design, often analyse their results before the final number of experimental units (humans, animals, tissues or cells) has been reached. If this is done in an uncontrolled fashion, the pejorative term 'peeking' has been applied. A statistical penalty must be exacted. This is because if enough interim analyses are conducted, and if the outcome of the trial is on the borderline between 'significant' and 'not significant', ultimately one of the analyses will result in the magical P = 0.05. I suggest that Armitage's technique of matched-pairs sequential analysis should be considered. The conditions for using this technique are ideal: almost unlimited opportunity for matched pairing, and a short time between commencement of a study and its completion. Both the Type I and Type II error-rates are controlled. And the maximum number of pairs necessary to achieve an outcome, whether P = 0.05 or P > 0.05, can be estimated in advance.

SUMMARY

Laboratory investigators, if they are to be honest, must adjust the critical value of P if they analyse their data repeatedly. I suggest they should consider employing matched-pairs sequential analysis in designing their experiments.

摘要

背景

在临床试验中,中期分析技术,即在结果仍在积累时进行的统计分析,已经高度发达。但在实验室实验中,此类分析通常是秘密进行的,且没有对I型错误率进行必要调整的规定。

讨论

实验室研究人员,无论是出于无知还是有意为之,常常在达到最终实验单位数量(人、动物、组织或细胞)之前就分析他们的结果。如果以一种不受控制的方式进行,就会被贴上贬义的“窥探”标签。必须施加统计惩罚。这是因为如果进行了足够多的中期分析,并且试验结果处于“显著”和“不显著”的临界值之间,最终其中一次分析将得出神奇的P = 0.05。我建议应该考虑阿米蒂奇的配对序贯分析技术。使用该技术的条件非常理想:几乎有无限的配对机会,并且研究开始和结束之间的时间很短。I型和II型错误率都能得到控制。而且无论结果是P = 0.05还是P > 0.05,实现该结果所需的最大配对数都可以提前估计。

总结

实验室研究人员,如果他们要诚实的话,在反复分析数据时必须调整P的临界值。我建议他们在设计实验时应考虑采用配对序贯分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1760/194709/f91f26deface/1471-2288-3-15-1.jpg

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