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首页> 外文期刊>Journal of Clinical Microbiology >Interlaboratory comparison of the toluidine red unheated serum test antigen preparation.
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Interlaboratory comparison of the toluidine red unheated serum test antigen preparation.

机译:甲苯胺红未加热血清测试抗原制剂的实验室间比较。

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The toluidine red unheated serum test (TRUST) antigen, a macroscopic flocculation test antigen developed by Pettit et al. (J. Clin. Microbiol. 18:1141-1145, 1983) by modifying the color-coded antigen of Kasatiya and Lambert (Appl. Microbiol. 28:317-318, 1974), was compared with the Venereal Disease Research Laboratory (VDRL) slide and rapid plasma reagin (RPR) 18-mm circle card tests for sensitivity, specificity, and reproducibility. Two lots of TRUST antigen were prepared by two laboratories in the Centers for Disease Control. Both laboratories performed the TRUST and VDRL slide test on serum samples from 1,102 patients attending the DeKalb County, Georgia, Sexually Transmitted Disease Clinic. In addition, one laboratory performed the RPR card test. Reactive sera were quantitated in the three nontreponemal tests and confirmed with the fluorescent treponemal antibody absorption test. The sensitivity in untreated syphilis for all nontreponemal tests involved was 98.4%. The specificity for these tests was 98.6%. The qualitative reproducibility among the four lots of TRUST antigen, VDRL slide, and RPR card tests was 98.2%. Only 20 sera showed discrepant results. Intralaboratory reproducibility of the two TRUST antigens was 100% for one laboratory and 99.6% for the other. Interlaboratory reproducibility for the four lots of TRUST and the VDRL slide test was 99%. Quantitative agreement +/- 1 dilution between the TRUST and RPR card test was 92.3%, and quantitative agreement +/- 1 dilution for the TRUST and RPR card test versus the VDRL slide test averaged 50%. The TRUST appeared to be comparable to the RPR card test in all parameters compared.
机译:甲苯胺红未加热血清测试(TRUST)抗原是由Pettit等人开发的一种宏观絮凝测试抗原。 (J. Clin。Microbiol。18:1141-1145,1983)通过修饰Kasatiya和Lambert的颜色编码抗原(Appl。Microbiol。28:317-318,1974)与性病研究实验室(VDRL)进行了比较。 )幻灯片和快速血浆反应素(RPR)18毫米圆卡测试,以进行敏感性,特异性和可重复性。疾病控制中心的两个实验室制备了两批TRUST抗原。两个实验室都对佐治亚州迪卡尔布县性传播疾病诊所的1,102名患者的血清样本进行了TRUST和VDRL玻片测试。另外,一个实验室进行了RPR卡测试。在三个非耳蜗测试中对反应性血清进行定量,并通过荧光性耳蜗抗体吸收测试进行确认。未经治疗的梅毒对所有涉及非梅毒测试的敏感性为98.4%。这些测试的特异性为98.6%。四批TRUST抗原,VDRL玻片和RPR卡测试之间的定性再现性为98.2%。仅20个血清显示出不一致的结果。两种TRUST抗原的实验室内再现性在一个实验室为100%,在另一实验室为99.6%。四个TRUST和VDRL玻片试验的实验室间重现性为99%。 TRUST和RPR卡测试之间的定量一致性+/- 1稀释度为92.3%,TRUST和RPR卡测试与VDRL玻片测试之间的定量一致性+/- 1稀释度平均为50%。在所有比较的参数上,TRUST看起来都与RPR卡测试相当。

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