校准对 Vitros XT 7600 分析仪 TSH 质量控制和患者结果偏差的影响。

Biochemia medica Pub Date : 2024-10-15 Epub Date: 2024-08-05 DOI:10.11613/BM.2024.030703
Jill Boreyko, Josko Ivica
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引用次数: 0

摘要

简介促甲状腺激素(TSH)是垂体前叶分泌的一种糖蛋白,受血清游离甲状腺激素的负反馈调节。在这项研究中,我们旨在量化 TSH Levey-Jennings 质量控制(QC)图表中校准漂移造成的相对偏差,并评估患者样本的偏差程度:在 2021 年 10 月至 2022 年 8 月期间,我们查看了 10 个 28 天校准时间间隔的质控结果,并计算了与平均值相比的相对偏差。对于每个时间间隔,计算校准前后三个质控点的平均值。计算校准前后 10 个平均值,然后计算校准前后的相对偏差。我们使用了 TSH 浓度较低、正常和较高的 5 份患者样本,并计算了校准前后的相对偏差。TSH 允许的相对偏差为 ± 6.7%:在两个质控水平上,平均值分别为 5.14 mIU/L(变异系数,CV% = 3.1%)和 27.80 mIU/L(CV% = 3.2%)的相对偏差分别为 - 8.2% 和 - 7.9%。低 TSH(0.586 mIU/L)、正常 TSH(2.89 mIU/L 和 5.19 mIU/L)和高 TSH(20.5 mIU/L 和 39.8 mIU/L)患者样本的相对偏差分别为-4.1%、-4.0%、-3.5%、-5.1%和-4.1%:尽管质控样本的相对偏差超过了允许的标准,但这在患者样本中并不明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The influence of calibration on bias in quality control and patient results for TSH on Vitros XT 7600 analyzer.

Introduction: Thyroid-stimulating hormone (TSH) is a glycoprotein secreted by the anterior pituitary gland and is regulated by negative feedback from the serum free thyroid hormones. In this study we aimed to quantitate the relative bias caused by calibration drifting as seen in our TSH Levey-Jennings quality control (QC) charts and assess the magnitude of bias on patients' samples.

Materials and methods: In the period from October 2021 to August 2022 we looked at the QC results of ten 28-days' calibration time intervals and calculated relative bias compared to the mean. For each time interval the mean from three QC points before and after calibration was calculated. The average from 10 pre- and post-calibration means was calculated and the relative bias, pre- and post-calibration, was then calculated. We used 5 patient samples with low, normal and high TSH concentrations and calculated relative bias pre- and post-calibration. The allowed relative bias for TSH is ± 6.7%.

Results: At both QC levels, with the respective means of 5.14 mIU/L (coefficient of variation, CV% = 3.1%) and 27.80 mIU/L (CV% = 3.2%) had their respective relative bias - 8.2% and - 7.9%. The patient samples with low (0.586 mIU/L), normal (2.89 mIU/L and 5.19 mIU/L) and high (20.5 mIU/L and 39.8 mIU/L) TSH had - 4.1%, - 4.0%, - 3.5%, - 5.1% and - 4.1%, respectively.

Conclusion: Even though the relative bias exceeded allowable criteria for the QC samples, this was not manifested on the patients' samples.

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