乙型肝炎表面抗原抗体定量常规检测的评价

S.C. Thompson , R.J. Warren , C.G. Ryan , D. Jolley
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引用次数: 0

摘要

澳大利亚微生物学会血清学特别兴趣小组对用于测量乙型肝炎表面抗原抗体(anti-HBs)的各种试剂盒进行了质量控制调查,原因是担心这些测试在实地的表现。共有20组血清,来自不同乙肝感染史和疫苗接种史的人,被分发到19个参与实验室,使用维多利亚州七种不同的商业抗乙肝检测方法(代表五家制造商)。受试者对重复采用盲法。分析了测定结果,以考虑雅培IMx方法的市场主导地位。一般来说,所有测试在测试范围内的线性度方面都执行得很好。测定内和测定间的可重复性表明,一些测定法在定量抗- hbs方面表现不充分。只有一个假阳性结果来自使用Amerlite的实验室,但在少数结果中,一个人的免疫状态会被错误地报告为无免疫。此外,使用相同放射免疫测定(RIA)试剂盒的两个实验室报告的单位不同,因此一个实验室报告的数值比另一个实验室报告的数值高6至12倍。这些结果突出表明,在没有向市场投放工具包颁发许可证的情况下,有必要进行统计上相关的独立评价,并不断监测实地的测试情况,包括参加应定期提供的质量保证活动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An evaluation of tests in routine use for the quantitation of antibody to hepatitis B surface antigen

A quality control survey of various kits for measuring antibody to hepatitis B surface antigen (anti-HBs) was undertaken by the Serology Special Interest Group of the Australian Society of Microbiology due to concern about the performance of these tests in the field. A total of 20 panels of sera, derived from people with diverse histories with respect to hepatitis B infection and vaccination, were distributed to 19 participating laboratories using seven different commercial anti-HBs assays (representing five manufacturers) throughout Victoria. Participants were blinded with respect to replicates. Assay results were analysed to take account of the market dominance of the Abbott IMx method. In general, all tests performed adequately with respect to linearity over the range tested. Reproducibility within and between assays shows that some assays are performing inadequately in the field for quantitating anti-HBs. There was only one false positive result, from a laboratory using Amerlite, but a small number of results where a person's immune status would have been falsely reported as non-immune. Additionally, the two laboratories which used the same radioimmunoassay (RIA) test kit reported in different units, so that numerically values six to 12 times higher were reported by one laboratory compared to the other. These results underscore the need for statistically relevant independent evaluation in the absence of the licensing of kits prior to market release, and ongoing monitoring of test performance in the field, including participation in quality assurance exercises which should be regularly available.

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