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Conventional Rapid Latex Agglutination in Estimation of von Willebrand Factor: Method Revisited and Potential Clinical Applications

机译:常规的快速乳胶凝集估计von Willebrand因子:检测方法和潜在临床应用

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Measurement of von Willebrand factor antigen (VWF?:?Ag) levels is usually performed in a specialised laboratory which limits its application in routine clinical practice. So far, no commercial rapid test kit is available for VWF?:?Ag estimation. This paper discusses the technical aspect of latex agglutination method which was established to suit the purpose of estimating von Willebrand factor (VWF) levels in the plasma sample. The latex agglutination test can be performed qualitatively and semiquantitatively. Reproducibility, stability, linearity, limit of detection, interference, and method comparison studies were conducted to evaluate the performance of this test. Semiquantitative latex agglutination test was strongly correlated with the reference immunoturbidimetric assay (Spearman's rho = 0.946, P < 0.001, n = 132). A substantial agreement ( κ = 0.77) was found between qualitative latex agglutination test and the reference assay. Using the scoring system for the rapid latex test, no agglutination is with 0% VWF?:?Ag (control negative), 1+ reaction is equivalent to 150% VWF?:?Ag (when comparing with immunoturbidimetric assay). The findings from evaluation studies suggest that latex agglutination method is suitable to be used as a rapid test kit for the estimation of VWF?:?Ag levels in various clinical conditions associated with high levels and low levels of VWF?:?Ag.
机译:通常在专门的实验室中进行von Willebrand因子抗原(VWF?:β-ag)水平的测量,这限制了其在常规临床实践中的应用。到目前为止,VWF没有商业快速测试套件?:?AG估计。本文讨论了乳胶凝集方法的技术方面,该方法是为了满足估算血浆样品中的von Willebrand因子(VWF)水平的目的。胶乳凝集试验可以定性和半定位进行。进行了再现性,稳定性,线性度,检测,干扰和方法比较研究,以评估该测试的性能。半静态胶乳凝集试验与参考免疫浊法测定强烈相关(Spearman的Rho = 0.946,P <0.001,N = 132)。在定性胶乳凝集试验和参考测定之间发现了大量的协议(κ= 0.77)。利用评分系统进行快速乳胶试验,没有凝集为0%VWF?:αAg(控制阴性),1+反应等同于150%VWF?:αAg(与免疫浊法比较时)。评估研究的发现表明,胶乳凝集方法适合用作估计VWF的快速试验套件?:βAG水平与高水平和低水平的临床病症相关的各种临床病症?:?AG。

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