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自动尿液颗粒分析仪的验证与核查

Validation and verification of automated urine particle analysers.

作者信息

Bignardi Giuseppe Enrico

出版信息

J Clin Pathol. 2017 Feb;70(2):94-101. doi: 10.1136/jclinpath-2016-203958. Epub 2016 Oct 31.

Abstract

There is often uncertainty on how validation and verification of newly introduced tests should be conducted, and there is a real risk of verification becoming a meaningless ritual, rather than a useful exercise. This article reviews the literature and makes recommendations regarding the validation and verification of automated urine particles analysers. A generic practical approach to verification is also recommended. For many analysers, the accuracy of white blood cells, epithelial cells and bacterial counts is corroborated by a number of independent evaluations; thus, any verification laboratory work could be significantly scaled down. Conversely, in the scenario that automated urine microscopy is used as a screening test to reduce the number of urines cultured, the extremely variable performance reported in the literature requires a full-scale verification to define the optimal cut-off values that give a sensitivity of >98% with the local settings and circumstances. With some analysers, the risk of carry-over also needs to be assessed, as part of the verification process, and exclusion criteria (urines requiring culture regardless of the microscopy results) need to be well defined, as there are patients or specimen types for which the performance of microscopy as a screening test may not be adequate.

摘要

对于新引入的检测如何进行验证和核查,常常存在不确定性,而且核查存在沦为无意义的例行公事而非有益实践的切实风险。本文回顾了相关文献,并就自动尿颗粒分析仪的验证和核查提出建议。还推荐了一种通用的核查实用方法。对于许多分析仪而言,白细胞、上皮细胞和细菌计数的准确性已得到多项独立评估的证实;因此,任何核查实验室工作都可大幅缩减。相反,如果将自动尿镜检用作减少培养尿液数量的筛查检测,文献中报道的性能差异极大,这就需要进行全面核查,以确定在当地环境和条件下能给出>98%灵敏度的最佳临界值。对于一些分析仪,作为核查过程的一部分,还需要评估携带污染风险,并且需要明确排除标准(无论镜检结果如何都需要培养的尿液),因为对于某些患者或标本类型,镜检作为筛查检测的性能可能并不充分。

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