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用于诊断传染性单核细胞增多症的试剂盒与保罗-邦内尔试验的比较。

Kits for the diagnosis of infectious mononucleosis compared with the Paul-Bunnell test.

作者信息

Uldall A, Jensen B S, Henrichsen J

机构信息

Department of Clinical Chemistry, University of Copenhagen, Herlev Hospital, Denmark.

出版信息

J Clin Chem Clin Biochem. 1990 Jun;28(6):423-5.

PMID:2212959
Abstract

We compared the results obtained with six different test kits for infectious mononucleosis with those obtained with the Paul-Bunnell test. The investigation was carried out in one laboratory using 149 selected pools of patient sera. Each pool was tested three times with the Paul-Bunnell test and once with each kit. The results obtained with the kits were grouped according to the titre found with the Paul-Bunnell test. The percentage of positive results within each group was calculated for each kit. The Paul-Bunnell titre, which would have classified 50% of the specimens as positive, was estimated for each kit and this was designated the 50% cut off value. In general, there was good agreement. However, false positive test results were found rather frequently with one kit (19%) and the 50% cut off values differed. One kit showed a 50% cut off value at about 8, another at about 16, and the rest at between 16 and 32. We suggest the introduction of improved internal quality control combined with external quality assessment.

摘要

我们将六种不同的传染性单核细胞增多症检测试剂盒的检测结果与保罗 - 邦内尔试验(Paul-Bunnell test)的结果进行了比较。该研究在一个实验室中进行,使用了149份选定的患者血清样本池。每个样本池用保罗 - 邦内尔试验检测三次,并用每种试剂盒检测一次。试剂盒检测所得结果根据保罗 - 邦内尔试验所发现的滴度进行分组。计算每种试剂盒在每组内的阳性结果百分比。估算每种试剂盒将50%的标本分类为阳性的保罗 - 邦内尔滴度,这被指定为50%临界值。总体而言,一致性良好。然而,发现有一种试剂盒经常出现假阳性检测结果(19%),并且50%临界值有所不同。一种试剂盒的50%临界值约为8,另一种约为16,其余的在16至32之间。我们建议引入改进的内部质量控制并结合外部质量评估。

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