UK NEQAS Haematology, West Herts Hospitals NHS Trust, Watford, UK.
The Leiden University Medical Center, Leiden, The Netherlands.
Int J Lab Hematol. 2021 Jun;43(3):494-499. doi: 10.1111/ijlh.13403. Epub 2020 Dec 2.
The accurate measurement of HbA is essential for the detection of β-thalassaemia carriers and as no single calibrant is used by the various manufacturers of analysers, differences are seen in results obtained. The World Health Organization International Reference Reagent for HbA (WHO IRR 89/666) was made available to diagnostic laboratories in the 1980s and remains the only international reference material available. A previous study (2015) demonstrated that the WHO IRR remained suitable for use as an HbA standard as tested by 52 participants in the UK NEQAS Haematology Abnormal Haemoglobins Programme. This study was undertaken to include simultaneous analysis of three whole blood specimens over a range of HbA values with the WHO IRR and to include participants from laboratories outside of the UK.
Three whole blood specimens with HbA levels ranging from 2.4% to 5.7% and the WHO IRR were distributed to 56 laboratories located in 14 different countries. Participants were requested to test the specimens at defined intervals and return results accompanied by chromatograms or electropherograms produced.
Differences found in results from different analyser groups reflect the bias found in the 2015 study in that bias is seen according to the methodology used and also varies in relation to the level of analyte being measured.
Results of measurements from whole blood specimens and the lyophilized WHO IRR standard did not show any deterioration of the IRR, and it remains suitable for use. Linearity and calibration of analysers remain a problem.
准确测量 HbA 对于检测 β-地中海贫血携带者至关重要,由于不同分析仪制造商使用的校准品各不相同,因此会得出不同的结果。1980 年代,世界卫生组织(WHO)的 HbA 国际参考试剂(WHO IRR 89/666)可供诊断实验室使用,它仍然是唯一可用的国际参考物质。先前的一项研究(2015 年)表明,WHO IRR 仍然适合用作 HbA 标准,英国 NEQAS 血液学异常血红蛋白计划的 52 名参与者对此进行了测试。本研究旨在包括使用 WHO IRR 对三种全血样本进行同时分析,样本的 HbA 值范围为 2.4%至 5.7%,并包括来自英国以外实验室的参与者。
将三种 HbA 水平在 2.4%至 5.7%之间的全血样本和 WHO IRR 分发给位于 14 个不同国家的 56 个实验室。要求参与者在规定的时间间隔内测试样本并返回附有产生的色谱图或电泳图的结果。
来自不同分析仪组的结果差异反映了 2015 年研究中的偏差,即偏差根据使用的方法学而有所不同,并且还与被测分析物的水平有关。
全血样本和冻干 WHO IRR 标准的测量结果并未显示 IRR 有任何恶化,它仍然适用。分析仪的线性度和校准仍然是一个问题。