专业止血中心出生聚集的影响因素和差异:多中心实验室比较的结果。

TH Open: Companion Journal to Thrombosis and Haemostasis Pub Date : 2022-08-22 eCollection Date: 2022-07-01 DOI:10.1055/a-1827-7025
Thorsten Kaiser, Karin Liebscher, Ute Scholz, Christian Pfrepper, Jeffrey Netto, Tim Drogies, Oliver Tiebel, Ralf Knöfler, Michael Krause
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引用次数: 0

摘要

光透射聚合法(LTA)被认为是血小板功能诊断的金标准。然而,在实际应用中存在一定程度的实验室间差异。目的建立一种可行的LTA实验室比较方法,分析5家专业止血中心在LTA标准化方面的差异及影响因素。方法对30例患者进行研究。每个中心使用诱导剂胶原蛋白(Col)、二磷酸腺苷(ADP)、花生四烯酸(ARA)和里斯托霉素对6名健康志愿者(3男3女)的血液样本进行LTA。LTA采用以下三种不同的方法进行:(1)国际血栓和止血学会推荐使用相同的试剂,(2)内部方案和相同的试剂;(3)内部方案和内部试剂。结果共进行了30个先证者的396次测量。即使在标准化方案和使用相同的试剂后,中心之间在最终和最大聚集方面存在显着差异(p = 0.002和p = p)。结论在本研究中,我们证明了使用的聚集仪,电感器浓度和制造商对最终和最大聚集有显着影响。这些结果说明了LTA标准化的挑战和重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influencing Factors and Differences in Born Aggregometry in Specialized Hemostaseological Centers: Results of a Multicenter Laboratory Comparison.

Introduction  Light transmission aggregometry (LTA) is regarded as the gold standard in platelet function diagnostics. However, there is a relevant degree of interlaboratory variability in practical applications. Objective  The aim of the present study was to develop a practicable laboratory comparison on LTA and to analyze differences and influencing factors in regard to standardization in five specialized hemostaseological centers. Methods  The study was performed on 30 patients in total. Each center performed LTA on blood samples from six healthy volunteers (three men and three women) using the inductors collagen (Col), adenosine diphosphate (ADP), arachidonic acid (ARA), and ristocetin. The LTA was performed three times using different methods as follows: (1) International Society on Thrombosis and Haemostasis recommendations with identical reagents, (2) in-house protocols and the identical reagents; and (3) in-house protocols and in-house reagents. Results  A total of 396 measurements of 30 probands were performed. Even after standardization of the protocol and using identical reagents, there were significant differences between the centers regarding the final and maximum aggregation ( p  = 0.002 and <0.001) and further significant differences in the maximum and final aggregation according to the wavelength of the device used to measure the LTA (PAP-8: 430 nm, APACT 4004: 740 nm [ p  < 0.001 each]). Using identical reagents but individual inductor concentrations and laboratory protocols also resulted in different maximum and final aggregation. The largest differences were seen with Col and ristocetin; there were significant influences from the reagents' manufacturers in the results of aggregometry for the inductor Col ( p  < 0.01) but not for ADP, ARA, and ristocetin. Conclusion  In this study, we proved that there are significant influences from the used aggregometers, inductors concentrations, and manufacturers. These results illustrate the challenges and importance of standardization of LTA.

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