Laboratory data in clinical trials: A statistician's perspective

被引:12
作者
Chuang-Stein, C [1 ]
机构
[1] Pharmacia & Upjohn Inc, Clin Dev Biostat 1, Kalamazoo, MI 49001 USA
来源
CONTROLLED CLINICAL TRIALS | 1998年 / 19卷 / 02期
关键词
laboratory toxicity; multicenter clinical trial; reference range; safety profile;
D O I
10.1016/S0197-2456(97)00123-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Even though laboratory data provide the best indicators for systemic toxicities in clinical trials of investigational medications, many applied statisticians lack a basic understanding of the interpretation of such data. Understanding is essential to a statistician's ability to help evaluate a patient's overall safety experience in a trial, the latter being the primary objective for collecting laboratory data in the trial. In this paper, we discuss the purpose of conducting laboratory evaluations as well as some hidden issues concerning the current practice of laboratory data analysis. The issues include the use of reference ranges, the one-parameter-at-a-time approach, and the exploratory nature of safety data analyses. (C) Elsevier Science Inc. 1998.
引用
收藏
页码:167 / 177
页数:11
相关论文
共 24 条