Jennen-Steinmetz C, Wellek S
Department of Biostatistics, Central Institute of Mental Health, University of Heidelberg, D-68072 Mannheim, Germany.
Stat Med. 2005 Oct 30;24(20):3199-212. doi: 10.1002/sim.2177.
A new criterion is proposed for determining the sample size required for a study performed for the purpose of establishing reference intervals. The basic idea behind the criterion is to compare the empirical coverage (i.e. the probability content) of the reference region obtained from the sample with its target value (e.g. 95 per cent) and to set suitable limits delta1, delta2 to the difference between both quantities which must not be exceeded with sufficiently large probability beta (e.g. beta=90 per cent). For the most frequently used parametric and distribution-free methods of estimating univariate reference limits, implicit formulae are derived relating the sample size to the design parameters delta1, delta2 and beta. For symmetric specification of (delta1, delta2), explicit approximation formulae for the computation of n are given. Exact values obtained by means of suitable numerical techniques are presented in a set of tables covering specifications of delta1, delta2 and beta which can be recommended for real applications. The tables can be used both for one- and two-sided reference intervals.
提出了一种新的标准,用于确定为建立参考区间而进行的研究所需的样本量。该标准背后的基本思想是将从样本中获得的参考区域的经验覆盖范围(即概率含量)与其目标值(例如95%)进行比较,并为这两个量之间的差异设置合适的界限δ1、δ2,在足够大的概率β(例如β = 90%)下,该差异不得超过此界限。对于最常用的估计单变量参考限的参数法和非参数法,推导了将样本量与设计参数δ1、δ2和β相关联的隐式公式。对于(δ1,δ2)的对称规格,给出了计算n的显式近似公式。通过合适的数值技术获得的精确值列于一组表格中,这些表格涵盖了δ1、δ2和β的规格,可推荐用于实际应用。这些表格可用于单侧和双侧参考区间。