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常规快速乳胶凝集法评估血管性血友病因子:方法回顾及潜在临床应用。

Conventional rapid latex agglutination in estimation of von Willebrand factor: method revisited and potential clinical applications.

机构信息

Departments of Haematology, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, 16150 Kubang Kerian, Kelantan, Malaysia.

Department of Immunology, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, 16150 Kubang Kerian, Kelantan, Malaysia.

出版信息

J Immunol Res. 2014;2014:850810. doi: 10.1155/2014/850810. Epub 2014 Dec 25.

DOI:10.1155/2014/850810
PMID:25759835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4352515/
Abstract

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 <20% VWF : Ag, and 4+ reaction indicates >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.

摘要

通常在专门的实验室中进行血管性血友病因子抗原(VWF: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,还没有用于 VWF:Ag 估计的商业快速检测试剂盒。本文讨论了乳胶凝集法的技术方面,该方法是为了适应在血浆样本中估计血管性血友病因子(VWF)水平的目的而建立的。乳胶凝集试验可定性和半定量进行。进行了重复性、稳定性、线性、检测限、干扰和方法比较研究,以评估该试验的性能。半定量乳胶凝集试验与参考免疫比浊测定法具有很强的相关性(Spearman's rho = 0.946,P < 0.001,n = 132)。定性乳胶凝集试验与参考测定法之间存在显著一致性(κ = 0.77)。使用快速乳胶测试的评分系统,无凝集为 0% VWF:Ag(对照阴性),1+反应相当于 <20% VWF:Ag,4+反应表示 >150% VWF:Ag(与免疫比浊测定法相比)。评估研究的结果表明,乳胶凝集法适合作为用于估计各种与 VWF:Ag 水平升高和降低相关的临床情况下的 VWF:Ag 水平的快速检测试剂盒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fafd/4352515/fdfc8dc109ae/JIR2014-850810.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fafd/4352515/fdfc8dc109ae/JIR2014-850810.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fafd/4352515/fdfc8dc109ae/JIR2014-850810.001.jpg

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