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四项凝血试验的外部质量评估控制物质的均匀性和稳定性评估

Homogeneity and Stability Evaluation of External Quality Assessment Control Materials for Four Coagulation Tests.

作者信息

Yuan Huimin, Gao Zhiqi, Zhang Jianping, Yue Yuhong, Zhang Shunli, Zhang Rui

出版信息

Clin Lab. 2021 May 1;67(5). doi: 10.7754/Clin.Lab.2020.200911.

Abstract

BACKGROUND

This study assessed the homogeneity and stability of control materials used in external quality assessment (EQA) of four coagulation tests, aiming to verify that these materials meet clinical testing requirements and to provide an evidence base for future improvement of laboratory coagulation test quality.

METHODS

The homogeneity and stability of control materials were assessed according to the relevant guidance. Homogeneity assessment involved 10 vials of samples obtained from 2 batches (each vial tested twice). The homogeneity of control materials in four coagulation tests was assessed using one-way analysis of variance, with standard deviation of uniformity (Ss) 0.3 σ as an assessment criterion. Stability assessment involved two vials of sam-ples obtained from two batches (each vial tested twice). The stability of control materials was assessed at cold storage, room temperature, temperature of 37°C. Reconstitution stability of control materials placed in cold storage and at room temperature, and long-term stability of reconstituted control materials stored frozen (-20°C and -80°C) were observed. Linear regression analysis was performed to assess long-term stability.

RESULTS

The Ss values of EQA control materials for four coagulation tests were PT L1 Ss = 0.084, PT L2 Ss = 0.889, APTT L1 Ss = 0.164, APTT L2 Ss = 0.223, Fbg L1 Ss = 6.256, Fbg L2 Ss = 2.251, TT L1 Ss = 0.552, TT L2 Ss = 0.3111. PT, APTT, Fbg, and TT were associated with the standard deviation of uniformity values of 0.3 σ. Non-reconstituted samples were observed at 37°C for 2 hours and 4 hours, and at room temperature for 1 day. Reconstituted samples were observed when stored at 4°C for 4 hours and 8 hours, at room temperature for 4 hours, and at -20°C and -80°C for 6 months. Instability of reconstituted samples was observed in PT and APTT tests at 4°C for 8 hours and at -20°C for 5 months.

CONCLUSIONS

EQA control materials presented with satisfactory homogeneity in four coagulation tests. Non-reconstituted samples presented with satisfactory stability at 37°C for 2 hours and 4 hours and at room temperature for 1 day, while reconstituted samples presented with satisfactory stability when refrigerated at 4°C for 4 hours, when kept at room temperature for 4 hours, and when frozen at -80°C for 6 months.

摘要

背景

本研究评估了四项凝血试验的外部质量评估(EQA)中所用对照材料的均匀性和稳定性,旨在验证这些材料是否符合临床检测要求,并为未来提高实验室凝血试验质量提供证据基础。

方法

根据相关指南评估对照材料的均匀性和稳定性。均匀性评估涉及从2个批次中获取的10瓶样品(每瓶测试两次)。使用单因素方差分析评估四项凝血试验中对照材料的均匀性,以均匀性标准差(Ss)0.3σ作为评估标准。稳定性评估涉及从两个批次中获取的两瓶样品(每瓶测试两次)。在冷藏、室温、37°C温度下评估对照材料的稳定性。观察了置于冷藏和室温下的对照材料的复溶稳定性,以及冷冻(-20°C和-80°C)保存的复溶对照材料的长期稳定性。进行线性回归分析以评估长期稳定性。

结果

四项凝血试验的EQA对照材料的Ss值分别为PT L1 Ss = 0.084,PT L2 Ss = 0.889,APTT L1 Ss = 0.164,APTT L2 Ss = 0.223,Fbg L1 Ss = 6.256,Fbg L2 Ss = 2.251,TT L1 Ss = 0.552,TT L2 Ss = 0.3111。PT、APTT、Fbg和TT与均匀性标准差0.3σ相关。未复溶的样品在37°C下观察2小时和4小时,在室温下观察1天。复溶后的样品在4°C下保存4小时和8小时、在室温下保存4小时、在-20°C和-80°C下保存6个月时进行观察。在4°C下保存8小时和在-20°C下保存5个月时,PT和APTT试验中观察到复溶样品不稳定。

结论

EQA对照材料在四项凝血试验中呈现出令人满意的均匀性。未复溶的样品在37°C下2小时和4小时以及在室温下1天呈现出令人满意的稳定性,而复溶后的样品在4°C下冷藏4小时、在室温下保存4小时以及在-80°C下冷冻6个月时呈现出令人满意的稳定性。

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