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西班牙分析前质量监测计划(SEQC):12年经验概述

Spanish Preanalytical Quality Monitoring Program (SEQC), an overview of 12 years' experience.

作者信息

Llopis María Antonia, Bauça Josep Miquel, Barba Nuria, Álvarez Virtudes, Ventura Montserrat, Ibarz Mercè, Gómez-Rioja Rubén, Marzana Itziar, Puente Juan Jose, Segovia Marta, Martinez Debora, Alsina María Jesús

出版信息

Clin Chem Lab Med. 2017 Mar 1;55(4):530-538. doi: 10.1515/cclm-2016-0382.

Abstract

BACKGROUND

Preanalytical variables, such as sample collection, handling and transport, may affect patient results. Preanalytical phase quality monitoring should be established in order to minimize laboratory errors and improve patient safety.

METHODS

A retrospective study (2001-2013) of the results obtained through the Spanish Society of Clinical Biochemistry and Molecular Pathology (SEQC) External quality assessment (preanalytical phase) was performed to summarize data regarding the main factors affecting preanalytical phase quality. Our aim was to compare data from 2006 to 2013 with a previously published manuscript assessing the 2001-2005 period.

RESULTS

A significant decrease in rejection rates was observed both for blood and urine samples. For serum samples, the most frequent rejection causes in the first period were non-received samples (37.5%), hemolysis (29.3%) and clotted samples (14.4%). Conversely, in the second period, hemolysis was the main rejection cause (36.2%), followed by non-received samples (34.5%) and clotted samples (11.1%). For urine samples, the main rejection cause overall was a non-received sample (up to 86.1% of cases in the second period, and 81.6% in the first). For blood samples with anticoagulant, the number of rejections also decreased. While plasma-citrate-ESR still showed the highest percentages of rejections (0.980% vs. 1.473%, p<0.001), the lowest corresponded to whole-blood EDTA (0.296% vs. 0.381%, p<0.001).

CONCLUSIONS

For the majority of sample types, a decrease in preanalytical errors was confirmed. Improvements in organization, implementation of standardized procedures in the preanalytical phase, and participation in a Spanish external quality assessment scheme may have notably contributed to error reduction in this phase.

摘要

背景

分析前变量,如样本采集、处理和运输,可能会影响患者检测结果。应建立分析前阶段质量监测,以尽量减少实验室误差并提高患者安全性。

方法

对通过西班牙临床生物化学与分子病理学学会(SEQC)外部质量评估(分析前阶段)获得的结果进行回顾性研究(2001 - 2013年),以总结有关影响分析前阶段质量的主要因素的数据。我们的目的是将2006年至2013年的数据与之前发表的评估2001 - 2005年期间的手稿中的数据进行比较。

结果

观察到血液和尿液样本的拒收率均显著下降。对于血清样本,第一阶段最常见的拒收原因是样本未收到(37.5%)、溶血(29.3%)和凝血样本(14.4%)。相反,在第二阶段,溶血是主要的拒收原因(36.2%),其次是样本未收到(34.5%)和凝血样本(11.1%)。对于尿液样本,总体主要拒收原因是样本未收到(第二阶段高达86.1%的病例,第一阶段为81.6%)。对于使用抗凝剂的血液样本,拒收数量也有所减少。虽然血浆 - 柠檬酸盐 - ESR的拒收率仍然最高(0.980%对1.473%,p<0.001),但最低的是全血EDTA(0.296%对0.381%,p<0.001)。

结论

对于大多数样本类型,分析前误差有所减少。组织方面的改进、分析前阶段标准化程序的实施以及参与西班牙外部质量评估计划可能对该阶段误差的减少有显著贡献。

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