Mazzo D J, Connolly M
Department of Analytical and Physical Chemistry, Rhône-Poulenc Rorer Central Research, Fort Washington, Pennsylvania 19034.
Pharm Res. 1992 May;9(5):601-6. doi: 10.1023/a:1015885607013.
Testing for the equivalence of results generated by different analytical methodology is a common practice in the pharmaceutical sciences. Methodology changes are implemented for both scientific and economic reasons during a scientific study. Thus, the need to demonstrate the appropriateness of considering data generated by distinct methods as part of a single information population arises. This paper describes a rapid and simple approach to the statistical design and interpretation of method comparison experiments. The approach presented is based upon a statistical power calculation technique, a knowledge of the variability associated with the methods to be compared and the criteria for equivalence (the limits within which differences become immeasurable or, for practical purposes, insignificant). Reference tables are included which show necessary sample sizes for comparison experiments for common combinations of these three variables.
检测不同分析方法所产生结果的等效性是制药科学中的常见做法。在科学研究过程中,出于科学和经济原因会实施方法变更。因此,就产生了需要证明将不同方法生成的数据视为单一信息总体一部分的合理性。本文描述了一种用于方法比较实验的统计设计和解释的快速简便方法。所提出的方法基于一种统计功效计算技术、对与待比较方法相关的变异性的了解以及等效性标准(差异变得不可测量或在实际应用中不显著的限度)。文中包含了参考表,这些表显示了这三个变量常见组合的比较实验所需的样本量。