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临床实验室检测标本短期稳定性的评估。

Evaluation of the short-term stability of specimens for clinical laboratory testing.

作者信息

Ikeda Katsuyoshi, Ichihara Kiyoshi, Hashiguchi Teruto, Hidaka Yoh, Kang Dongchon, Maekawa Masato, Matsumoto Hiroyuki, Matsushita Kazuyuki, Okubo Shigeo, Tsuchiya Tatsuyuki, Furuta Koh

机构信息

1 Department of Clinical Laboratory, Kumamoto University Hospital Faculty of Health Sciences , Kumamoto, Japan .

出版信息

Biopreserv Biobank. 2015 Apr;13(2):135-43. doi: 10.1089/bio.2014.0072.

Abstract

BACKGROUND

A major concern in both the laboratory-medicine and research communities is the quality of human specimens for analysis. However, there is insufficient scientific evidence regarding optimal conditions for handling and storing routine specimens, especially those in liquid form. Thus, we investigated the stability of clinically relevant samples stored under various conditions.

MATERIALS AND METHODS

Ten clinical laboratories in Japan conducted analyses of the stability of post-clinical (left over after analysis) test samples in relation to temperature and storage duration. We examined serum, whole blood, and urine samples submitted to each laboratory for routine testing. In this study, at least 5 samples for each of 35 tests were analyzed at each laboratory. After completion of routine testing, specimens with sufficient residual volume and values between LL-R/2 (lower limit of reference interval) and UL+R/2 (upper limit) were divided into 300 μL aliquots, where R=UL - LL. Aliquots of serum specimens were stored at either room temperature (23°C), 4°C, -20°C, or -80°C without light exposure. Aliquots of whole blood and urine specimens were stored at either 23°C or 4°C. The storage time was either 1, 3, or 7 days. Average differences between pre- and post-storage test results were evaluated for each laboratory test by two-way ANOVA. F-values for between-day variations were used for judging the statistical significance of storage-related changes in test values, whereas the ratio of between-day SD to between-individual SD (one-fourth of reference interval) was used to indicate the practical significance of the change.

RESULTS AND CONCLUSION

Sample denaturation is clearly temperature- and storage-duration dependent for almost all analytes. In general, specimens were most susceptible to denaturation at 23°C, then 4°C, -20°C, and -80°C. This study confirmed the accumulated routine, practice-based, detailed knowledge regarding specimen stability and will help to ensure the reliability of laboratory test results.

摘要

背景

检验医学和研究领域的一个主要关注点是用于分析的人体标本质量。然而,关于处理和储存常规标本(尤其是液体形式的标本)的最佳条件,科学证据不足。因此,我们研究了在各种条件下储存的临床相关样本的稳定性。

材料与方法

日本的10个临床实验室对临床后(分析后剩余)检测样本在温度和储存时间方面的稳定性进行了分析。我们检查了提交给每个实验室进行常规检测的血清、全血和尿液样本。在本研究中,每个实验室对35项检测中的每项至少分析5个样本。常规检测完成后,将剩余体积足够且值在参考区间下限(LL-R/2)和上限(UL+R/2)之间的标本分成300μL的等分试样,其中R = UL - LL。血清标本的等分试样在室温(23°C)、4°C、-20°C或-80°C下避光储存。全血和尿液标本的等分试样在23°C或4°C下储存。储存时间为1天、3天或7天。通过双向方差分析评估每个实验室检测在储存前后检测结果的平均差异。日间变化的F值用于判断检测值中与储存相关变化的统计学意义,而日间标准差与个体间标准差(参考区间的四分之一)的比值用于表明变化的实际意义。

结果与结论

几乎所有分析物的样本变性都明显取决于温度和储存时间。一般来说,标本在23°C时最易变性,其次是4°C、-20°C和-80°C。本研究证实了关于标本稳定性的积累的常规、基于实践的详细知识,并将有助于确保实验室检测结果的可靠性。

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