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从新鲜且从未冷冻的血浆开始,在Cobas t 711分析仪上测定一系列广泛的凝血参数和因子检测的样本稳定性。

Determination of sample stability for a broad panel of coagulation parameters and factor assays on the Cobas t 711 analyzer starting from fresh-never-frozen plasma.

作者信息

Hoffmann Michael, Gottschalk Norbert, Huber Philipp, Scheling Vanessa, von Allmen Nicole, Hegel J Kolja

机构信息

Roche Diagnostics GmbH, Penzberg, Germany.

Roche Diagnostics International Ltd., Rotkreuz, Switzerland.

出版信息

Front Mol Biosci. 2025 Apr 3;12:1491239. doi: 10.3389/fmolb.2025.1491239. eCollection 2025.

Abstract

BACKGROUND

Preanalytical procedures can affect the accuracy of coagulation assay results. Recommended plasma storage temperatures and durations need to be defined for individual coagulation assays. Here, we evaluated the effect of commonly applied plasma storage conditions for a broad panel of 23 basic coagulation parameters as well as specialized factor assays developed for the Cobas t 711 analyzer (Roche Diagnostics International Ltd., Rotkreuz, Switzerland).

METHODS

This single-center, prospective, observational study used anonymized, residual, platelet-poor plasma samples as well as pseudonymized plasma samples to obtain rare ranges of certain analytes. Fresh-never-frozen plasma samples processed within 4 h were tested in triplicate at time zero (t), with measurements repeated at various predefined timepoints after storage at 18-25°C, 2-8°C, or under freezing and deep freezing. Mean deviation from t, expressed as a percentage or as absolute change in signal at very low analyte levels, was assessed against predefined, assay-specific acceptance criteria for each analyte.

RESULTS

The sample stability results under the examined storage conditions for all 23 assays met or exceeded the requirements for routine laboratory coagulation testing and the respective acceptance criteria for each individual assay were fulfilled. Fresh-never-frozen samples were used to reflect real-life laboratory settings, enabling the early detection of out-of-specification results.

CONCLUSION

Sample stability was determined for a broad panel of assays on the t 711 analyzer, for application in routine coagulation testing practice.

摘要

背景

分析前程序会影响凝血检测结果的准确性。需要为各个凝血检测确定推荐的血浆储存温度和时长。在此,我们评估了常用血浆储存条件对23项基本凝血参数以及为Cobas t 711分析仪(罗氏诊断国际有限公司,瑞士罗特kreuz)开发的特定因子检测的影响。

方法

这项单中心、前瞻性、观察性研究使用匿名的、剩余的、少血小板血浆样本以及化名血浆样本,以获取某些分析物的罕见范围。在4小时内处理的新鲜且从未冷冻的血浆样本在时间零点(t)进行一式三份检测,并在18 - 25°C、2 - 8°C或冷冻及深度冷冻储存后的各个预定义时间点重复测量。根据每种分析物的预定义、特定检测接受标准,评估相对于t的平均偏差,以百分比形式或在极低分析物水平下信号的绝对变化形式表示。

结果

在所有23项检测的所检查储存条件下,样本稳定性结果均达到或超过常规实验室凝血检测的要求,并且满足了每项单独检测的各自接受标准。使用新鲜且从未冷冻的样本以反映实际实验室环境,从而能够早期检测出不符合规格的结果。

结论

确定了t 711分析仪上一系列广泛检测的样本稳定性,以应用于常规凝血检测实践。

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