Using tolerance limits to evaluate laboratory data

被引:0
|
作者
Nickens, DJ [1 ]
机构
[1] Pharmacia & Upjohn Inc, Clin Biostat 2, Kalamazoo, MI 49001 USA
来源
DRUG INFORMATION JOURNAL | 1998年 / 32卷 / 01期
关键词
tolerance limits; clinical trials; safety laboratories; sample size;
D O I
暂无
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Quantitative laboratory measurements are a large parr of the data collected in a clinical trial and the analysis of this type of data is often challenging. The use of tolerance limits and its variations, which describe the concentration and extremes of a distribution, provide useful methods to evaluate laboratory data. The theory of tolerance limits far the gaussian distribution and any unknown continuous distribution is presented. Tolerance limits provide adequate data reduction while still allowing appropriate interpretation of the results and are useful for evaluating individual patient responses. Examples of the utility of determining limits in which a chosen proportion of the data is likely to be concentrated for interpretation purposes are presented Using the concept of tolerance limits to determine the size of a clinical trial designed from the safety perspective is also discussed.
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页码:261 / 269
页数:9
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