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首页> 外文期刊>Scandinavian journal of clinical and laboratory investigation. >Allowable bias derived from the NOBIDA reference values
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Allowable bias derived from the NOBIDA reference values

机译:允许偏差来自Nobida参考值

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摘要

Figures of allowable bias are used to make rational choices of quality control rules, to judge the validity of published reference values, and to determine the stability of sample materials. Usually, allowable bias is parametrically defined as 0.25 times the total biological standard deviation, because that is half the width of the 90% confidence interval of parametrically estimated reference limits from 120 reference values. The published figures are mostly derived from very small populations, less than 120. We estimated allowable bias non-parametrically as the least of 4 percentile differences in distributions of reference values from the large Nordic reference interval project biobank and database (NOBIDA). The percentile differences are equivalent to 0.25 times the total biological standard deviation in Gaussian distributions. We also estimated allowable bias from the distributions of non-parametrically estimated reference limits after resampling 120 reference values from the same datasets. Clearly larger allowable bias was derived from the resampling method than from the percentile difference method, showing that non-parametric estimation of reference limits from 120 reference values implies a larger allowable bias than 0.25 times the normal biological standard deviation. With some exceptions, the figures of allowable bias using the percentile difference method were in the same order of magnitude as parametrically derived figures in other studies, and lend some support to the results from those smaller studies. Whether such bias specifications, if met, guarantee measurements of sufficient clinical quality is unknown.
机译:允许偏差的数字用于制造质量控制规则的合理选择,以判断公布的参考值的有效性,并确定样品材料的稳定性。通常,允许偏压参数定义为总生物标准偏差的0.25倍,因为这是来自120参考值的参数估计参考限制的90%置信区间的宽度的一半。已发布的数字主要来自非常小的群体,小于120.我们估计了允许的偏差非参数偏差,因为来自大型北欧参考间隔项目Biobank和数据库(Nobida)的参考值分布的至少4个百分点。百分位差异相当于高斯分布中生物标准偏差的0.25倍。在重新采样120参考值之后,我们还估计了从来自相同数据集的120参考值之后的非参数估计参考限制的分布允许的偏置。显然较大的允许偏置从重采样方法中得出多于百分位差异方法,示出了来自120参考值的参考限制的非参数估计意味着比正常生物标准偏差的0.25倍更大的允许偏置。在一些例外,使用百分位差异方法的允许偏差的图与其他研究中的参数衍生的图形相同的数量级,并对这些较小研究的结果提供一些支持。无论是这种偏置规格,如果满足,则保证足够的临床质量的测量。

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