Working Group for Post-analytics, Croatian Society of Medical Biochemistry and Laboratory Medicine, Zagreb, Croatia.
Department of Transfusion Medicine and Transplantation Biology, University Hospital Centre Zagreb, Zagreb, Croatia.
Biochem Med (Zagreb). 2020 Jun 15;30(2):020702. doi: 10.11613/BM.2020.020702. Epub 2020 Apr 15.
Autovalidation (AV) is an algorithm based on predefined rules designed, among others, to automate and standardize the postanalytical phase of laboratory work. The aim of this study was to examine the overall opinion of Croatian medical biochemistry laboratories regarding various aspects of AV.
This retrospective study is an analysis of the responses of a survey about AV comprised of 18 questions, as part of Module 10 ("Postanalytical phase of laboratory testing") of national External Quality Assessment program, administered by the Croatian Centre for Quality Assessment in Laboratory Medicine. Results were reported as percentages of total number of participants in survey or as proportions of observed data if the overall number of data was <100.
121 laboratories responded to the survey, of which 76% do not use AV, while 11% of laboratories use AV in routine laboratory work. 16/29 laboratories implemented semi-automated AV for general biochemistry (7/29), haematology (5/29), and coagulation (4/29) tests. Analytical measurement ranges, critical values, flags from analysers, interference indices and delta check were the most commonly used rules in the algorithm. 12/29 laboratories performed validation of AV with less than 500 samples (8/29). 7/13 laboratories report the percentage of AV being 20-50%, while 10/13 answered that introduction of AV significantly reduced turnaround time (TAT) (for 20 - 25%), especially for biochemistry tests.
Despite of its numerous benefits ( shorter TAT, less manual validation, standardization of the postanalytical phase), only a small number of Croatian laboratories use AV.
自动验证(AV)是一种基于预定义规则的算法,旨在实现实验室分析后阶段的自动化和标准化。本研究旨在调查克罗地亚医学生物化学实验室对 AV 各个方面的总体看法。
这是一项回顾性研究,分析了全国体外质量评估计划模块 10(实验室检测的分析后阶段)中包含 18 个问题的 AV 调查应答,该计划由克罗地亚实验室医学质量评估中心管理。结果以应答调查的总参与者人数的百分比或如果观察到的数据总数<100,则以观察数据的比例报告。
121 个实验室对该调查做出了应答,其中 76%的实验室不使用 AV,而 11%的实验室将 AV 常规应用于实验室工作。29 个实验室中的 16 个实施了用于常规生化(7/29)、血液学(5/29)和凝血(4/29)检验的半自动化 AV。分析测量范围、临界值、来自分析仪的标记、干扰指数和 delta 检查是算法中最常用的规则。29 个实验室中的 12 个仅用<500 个样本对 AV 进行了验证(8/29)。29 个实验室中的 7 个报告 AV 百分比为 20-50%,而 13 个实验室中的 10 个回答称 AV 的引入显著缩短了周转时间(TAT)(对于 20-25%),特别是对于生化检验。
尽管 AV 具有许多优势(更短的 TAT、更少的手动验证、分析后阶段的标准化),但只有少数克罗地亚实验室使用 AV。