Sample size determination for equivalence test using rate ratio of sensitivity and specificity in paired sample data

被引:20
作者
Lui, KJ
Cumberland, WG
机构
[1] San Diego State Univ, Coll Sci, Dept Math & Comp Sci, San Diego, CA 92182 USA
[2] Univ Calif Los Angeles, Dept Biostat, Los Angeles, CA 90024 USA
来源
CONTROLLED CLINICAL TRIALS | 2001年 / 22卷 / 04期
关键词
bioequivalence; power; type I error; sample size determination; sensitivity; specificity;
D O I
10.1016/S0197-2456(01)00134-9
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
Before implementing a new diagnostic test, we may wish to study whether this test is noninferior to a reference test with respect to the sensitivity and/or the specificity. This paper discusses sample size determination for one-sided equivalence (or noninferiority) testing of the rate ratio using paired-sample data. Using large sample theory, this paper derives asymptotic sample size formulae for the required number of subjects giving a desired power 100(1 - beta)% at a specified a-level. To evaluate the accuracy of these formulae, this paper considers several test statistics and uses Monte Carlo simulation to estimate the corresponding type I error and power with the given resulting sample sizes in a variety of situations. Finally, this paper notes those situations for which the asymptotic sample size formulae developed here are of limited use and suggests a simple empirical adjustment to alleviate this limitation. (C) Elsevier Science Inc. 2001.
引用
收藏
页码:373 / 389
页数:17
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