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一项关于商业和内部抗心磷脂抗体检测方法的批内和批间变异的多中心评估。

A multi-centre evaluation of the intra-assay and inter-assay variation of commercial and in-house anti-cardiolipin antibody assays.

作者信息

Wong Richard, Favaloro Emmanuel, Pollock Wendy, Wilson Robert, Hendle Michelle, Adelstein Stephen, Baumgart Karl, Homes Paul, Smith Stuart, Steele Richard, Sturgess Allan, Gillis David

机构信息

Division of Immunology, Queensland Health Pathology Services, Princess Alexandra and Royal Brisbane Hospitals, Qld, Australia.

出版信息

Pathology. 2004 Apr;36(2):182-92. doi: 10.1080/00313020410001672037.

Abstract

AIMS

To assess the intra-assay (intra-run) and inter-assay (inter-run) variation of commercial and in-house IgG and IgM anti-cardiolipin antibody (aCL) assays/kits, and to determine an appropriate maximum value for inclusion in consensus guidelines.

METHODS

Frozen aliquots of two patient specimens and one commercial control were sent to nine laboratories for the evaluation of eight commercial kits and one in-house assay. Intra-assay and inter-assay evaluations were performed with all three samples for IgG aCL, and one patient specimen for IgM aCL.

RESULTS

The IgG and IgM aCL values varied considerably between the nine assays/kits. The majority of assays/kits demonstrated less than 20% intra-assay and inter-assay variation, with lower intra-assay and inter-assay variation observed with the commercial control. Single calibrator assays were not consistently associated with higher inter-assay variation than multi-point calibrator assays.

CONCLUSIONS

An inter-assay coefficient of variation of 20% was determined to be an appropriate maximum value for inclusion in the Australasian aCL Working Party consensus guidelines. Improved standardisation between different assay/kits is still required.

摘要

目的

评估市售及自制的IgG和IgM抗心磷脂抗体(aCL)检测方法/试剂盒的批内(同批测定)和批间(不同批次测定)变异,并确定纳入共识指南的合适最大值。

方法

将两份患者标本和一份市售对照的冷冻分装样本送至九个实验室,用于评估八种市售试剂盒和一种自制检测方法。对所有三个样本进行IgG aCL的批内和批间评估,对一份患者标本进行IgM aCL的评估。

结果

九种检测方法/试剂盒之间的IgG和IgM aCL值差异很大。大多数检测方法/试剂盒的批内和批间变异小于20%,市售对照的批内和批间变异更低。单校准品检测方法与多点校准品检测方法相比,批间变异不一定更高。

结论

批间变异系数20%被确定为纳入澳大利亚aCL工作组共识指南的合适最大值。不同检测方法/试剂盒之间仍需改进标准化。

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