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Acceptable variability in external quality assessment programmes for basic semen analysis

机译:用于基本精液分析的外部质量评估计划中的可接受变异

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BACKGROUND: External quality assessment is essential in modern andrology laboratories. To assess the proficiency of laboratories participating in an external quality assessment programme (EQAP), limits for acceptable variability must be determined. Limits currently specified largely depend on criteria set by the organizers of individual EQAP schemes. The objective of this study was to evaluate the different criteria described in ISO 13528: 2005 for calculating acceptable variability in EQAP when applied to basic semen analysis parameters. METHODS: AND RESULTSThe data used in this study were the means and standard deviations obtained for independent samples from two EQAPs, one national (Spanish) and one international (European). The acceptable variability according to ISO 13528: 2005 was calculated using four types of criteria: (i) ±3 standard deviations of the results of all participating laboratories; (ii) ±3 standard deviations of the results of expert laboratories; (iii) quality specifications based on biological variability, state-of-the-art and clinicians' opinions and (iv) the same quality specifications adjusted for the uncertainty of the assigned value. The first two strategies resulted in very wide ranges of acceptable variability. Conversely, the strategy based only on quality specifications resulted in very narrow ranges. For the fourth strategy, acceptable ranges were intermediate between the results produced with the other strategies. The third and fourth strategies did not produce observable differences in acceptable ranges when the model used for calculating the specifications of analytical quality was changed. CONCLUSIONS: It is essential that EQAPs for semen parameters should determine the ranges for acceptable variability in results. Moreover, these ranges must be clinically useful, i.e. the variability should have a minimal negative impact on clinical decisions. The exact definition of 'expert laboratory' is more important than the model chosen for estimating analytical quality specifications in an EQAP for semen parameters in basic semen analysis.
机译:背景:外部质量评估在现代男科学实验室至关重要。为了评估参与外部质量评估计划(EQAP)的实验室的熟练程度,必须确定可接受的变异性极限。当前指定的限制很大程度上取决于各个EQAP计划的组织者设定的标准。这项研究的目的是评估ISO 13528:2005中描述的不同标准,以计算当应用于基本精液分析参数时EQAP的可接受变异性。方法和结果本研究中使用的数据是从两个EQAP(一个国家(西班牙)和一个国际(欧洲))获得的独立样品的均值和标准差。根据ISO 13528:2005,使用四类标准计算了可接受的变异性:(i)所有参与实验室的结果的±3标准偏差; (ii)专家实验室结果的±3标准偏差; (iii)根据生物学变异性,最新技术和临床医生的意见制定的质量规范,以及(iv)针对指定值的不确定性进行调整的相同质量规范。前两种策略导致可接受的变异范围非常广。相反,仅基于质量规格的策略导致范围非常狭窄。对于第四个策略,可接受的范围介于其他策略产生的结果之间。当更改用于计算分析质量指标的模型时,第三种和第四种策略在可接受范围内没有产生可观察到的差异。结论:精液参数的EQAPs必须确定可接受的结果变异范围。此外,这些范围必须在临床上有用,即变异性对临床决策的负面影响应最小。 “专家实验室”的准确定义比为基本精液分析中的精液参数在EQAP中估算分析质量规格所选择的模型更为重要。

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