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血浆甲氧基肾上腺素的初步质量保证计划。

Pilot quality assurance programme for plasma metanephrines.

机构信息

Department of Clinical Chemistry, SEALS, The Prince of Wales Hospital, Randwick, Australia.

出版信息

Ann Clin Biochem. 2010 Mar;47(Pt 2):137-42. doi: 10.1258/acb.2009.009153. Epub 2010 Feb 9.

Abstract

BACKGROUND

Up to 2007 there was no formal external quality assurance programme for plasma free metanephrines. A pilot programme was conceived by the AACB (Australian Association of Clinical Biochemists) Working Party on biogenic amines. With support from the AACB and Royal College of Pathologists of Australasia Quality Assurance programmes, a pilot study was developed. Data from this study are presented for the first time.

METHODS

Twelve lyophilized plasma samples were distributed to 15 centres. Samples were spiked with metanephrine (metadrenaline), normetanephrine (normetadrenaline) and 3-methoxytyramine, all derived from human urine. Concentrations were arranged in a linear relationship. The analytes were present at six levels and samples were duplicated.

RESULTS

High-pressure liquid chromatography and tandem mass spectrometry methods showed acceptable precision but in general enzyme immunoassay displayed a higher degree of imprecision as well as a negative bias.

CONCLUSIONS

Differences in calibration and matrix effects are likely to have been responsible for the discrepancy between chromatographic and immunoassay methods. These differences need to be further examined although efforts at standardization between different methods have been hampered by the lack of a universal calibrator for plasma metanephrines. Meanwhile, a laboratory's performance characteristics can be monitored and enhanced by participation in suitable external quality assurance programmes.

摘要

背景

截至 2007 年,还没有针对血浆游离甲氧基肾上腺素的正式外部质量保证计划。澳大利亚临床生物化学家协会(AACB)生物胺工作组构思了一个试点计划。在 AACB 和澳大利亚和新西兰皇家病理学院质量保证计划的支持下,开展了一项试点研究。首次提交了该研究的数据。

方法

将 12 份冷冻干燥的血浆样本分发给 15 个中心。向样本中添加了甲氧基肾上腺素(间肾上腺素)、去甲甲氧基肾上腺素(去甲间肾上腺素)和 3-甲氧基酪胺,所有这些均来自人类尿液。浓度呈线性关系。分析物存在于六个水平,且样本进行了重复。

结果

高效液相色谱和串联质谱法显示出可接受的精密度,但一般酶免疫测定法显示出更高的不精密度以及负偏差。

结论

校准和基质效应的差异可能是色谱和免疫测定法之间存在差异的原因。尽管由于缺乏用于血浆甲氧基肾上腺素的通用校准器,不同方法之间的标准化努力受到阻碍,但仍需要进一步检查这些差异。同时,实验室的性能特征可以通过参与合适的外部质量保证计划来进行监测和增强。

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