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External quality assessment of pertussis serology in Germany

机译:德国百日咳血清学的外部质量评估

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摘要

The purpose of this investigation was to test the performance of pertussis serology in diagnostic laboratories. The World Health Organization (WHO) Reference Reagent (06/142) and a sample with a low level of antibodies were sent to 200 participants of an external quality assessment (EQA) programme in Germany. The results were reported qualitatively and quantitatively, and were converted into IU/ml when possible. A total of 183 participants reported results. IgG, IgA and IgM enzyme-linked immunosorbent assays (ELISAs) with mixed antigens were used by 111, 110 and 113 participants, respectively, and 69 and 44 participants used IgG and IgA ELISAs with purified pertussis toxin (PT), respectively. IgG, IgA and IgM immunoblots were employed by 62, 63 and 11 participants, respectively. Most tests could distinguish between the positive and negative samples, but quantitative results were reported partly in non-comparable units. Only 37 % of participants used ELISAs that gave results comparable to the expected values in IU/ml and that could be interpreted according to published recommendations.
机译:这项研究的目的是在诊断实验室测试百日咳血清学的性能。世界卫生组织(WHO)参考试剂(06/142)和抗体含量低的样品已发送给德国外部质量评估(EQA)计划的200名参与者。对结果进行定性和定量报告,并在可能的情况下转换为IU / ml。共有183位参与者报告了结果。 111、110和113位参与者分别使用了具有混合抗原的IgG,IgA和IgM酶联免疫吸附测定(ELISA),69和44位参与者分别使用了带有纯化的百日咳毒素(PT)的IgG和IgA ELISA。分别有62、63和11名参与者使用了IgG,IgA和IgM免疫印迹。大多数测试可以区分正样本和负样本,但定量结果部分以不可比较的单位报告。只有37%的参与者使用ELISA产生的结果与IU / ml的预期值相当,并且可以根据已发布的建议进行解释。

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