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首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Effect of analytical run length on quality-control (QC) performance and the QC planning process
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Effect of analytical run length on quality-control (QC) performance and the QC planning process

机译:分析运行长度对质量控制(QC)性能和质量控制计划过程的影响

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The performance measure traditionally used in the quality-control (QC) planning process is the probability of rejecting an analytical run when an out-of-control error condition exists. A shortcoming of this performance measure is that it doesn’t allow comparison of QC strategies that define analytical runs differently. Accommodating different analytical run definitions is straightforward if QC performance is measured in terms of the average number of patient samples to error detection, or the average number of patient samples containing an analytical error that exceeds total allowable error. By using these performance measures to investigate the impact of different analytical run definitions on QC performance demonstrates that during routine QC monitoring, the length of the interval between QC tests can have a major influence on the expected number of unacceptable results produced during the existence of an out-of-control error condition.
机译:传统上在质量控制(QC)计划过程中使用的性能度量是存在失控错误情况时拒绝分析运行的可能性。这项绩效指标的一个缺点是,它不允许比较以不同方式定义分析运行的质量控制策略。如果根据要进行错误检测的患者样本的平均数量或包含分析误差超过总允许误差的患者样本的平均数量来衡量QC性能,则可以轻松地适应不同的分析运行定义。通过使用这些性能指标来调查不同的分析运行定义对QC性能的影响,表明在常规QC监测过程中,两次QC测试之间的间隔时间长度可能会对预期存在的不可接受结果的数量产生重大影响。失控错误条件。

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