How to achieve standardization of statistical methods in toxicology

被引:0
作者
Healey G.F. [1 ]
机构
[1] Head of Statistics, Huntingdon Life Sciences, Huntingdon, Cambs, PE18 6ES
来源
Drug information journal : DIJ / Drug Information Association | 1997年 / 31卷 / 2期
关键词
Performance criteria; Standardization; Statistical methodology; Statistical power; Toxicology;
D O I
10.1177/009286159703100210
中图分类号
学科分类号
摘要
The current diversity in statistical methodology for even quite simple situations is emphasized. The reasons for this diversity can be grouped into two broad categories: Cultural, including national preference, historical precedent, and resource availability; and statistical, including inadequacies in statistical theory, inadequate knowledge of the biological context, and other practical constraints. Although criteria for an ideal methodology could be defined, no current methods satisfy them and are therefore suboptimal. It is inferred that to attempt worldwide standardization on a particular statistical test in a particular situation (“Standardization by Method”) is generally not desirable. A proposal will be made, however, that it should be possible to achieve standardization by the setting of “performance criteria” in order to classify proposed methods as “acceptable” or “unacceptable” (“Standardization by Performance”). © 1997, Drug Information Association. All rights reserved.
引用
收藏
页码:395 / 401
页数:6
相关论文
共 6 条
[1]  
Box G.E.P., Robustness in the Strategy of Scientific Model Building, Robustness in Statistics, (1979)
[2]  
Williams D.A., A test for differences between treatment means when several dose levels are compared with a zero dose control, Biometrics, 27, pp. 103-117, (1971)
[3]  
Snedecor G.W., Cochran W.G., Statistical Methods, 1980
[4]  
Dunnett C.W., New tables for multiple comparisons with a control, Biometrics, 20, pp. 482-491, (1964)
[5]  
Armitage P., Statistical Methods in Medical Research, (1971)
[6]  
SAS/STAT User's Guide, 2, (1989)