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自动化光传输聚集仪的评估。

Evaluation of an automated light transmission aggregometry.

机构信息

a West China School of Medicine/West China Hospital , Sichuan University , Chengdu , P.R. China.

b Department of Laboratory Medicine , West China Hospital, Sichuan University , Chengdu , P.R. China.

出版信息

Platelets. 2017 Nov;28(7):712-719. doi: 10.1080/09537104.2016.1265923. Epub 2017 Feb 2.

Abstract

Light transmission aggregometry (LTA) is the "gold standard" for platelet function assessment, but it is time-consuming and labor intensive. Recently, an automated platelet aggregation method has been developed on a routine coagulation analyzer (Sysmex CS-2100i). In this study, the performances of CS-2100i including repeatability, correlation with a reference aggregometer (Chrono-log Model 700), and the threshold limitation of platelet counts in platelet-rich plasma (PRP) were evaluated for clinical use. The agonists were adenosine diphosphate (ADP), arachidonic acid, collagen, epinephrine, and ristocetin. The platelet concentration of PRP was adjusted with platelet-poor plasma (PPP) and physiological saline (PS). The CS-2100i showed an excellent repeatability and a strong correlation with the Chrono-log 700 in performing platelet aggregation, and its threshold limitation of platelet counts in PRP was 80 × 10/L. PPP had an inhibitory impact on platelet aggregation induced by ADP, arachidonic acid, collagen or epinephrine; while PS had an inhibitory impact on ristocetin-induced aggregation. PS should be used to adjust PRP for ADP-, arachidonic acid-, collagen-, or epinephrine-induced aggregation; while PPP was recommended for ristocetin-induced aggregation. The CS-2100i showed an excellent repeatability, a strong correlation with Chrono-log 700, a lower platelet count requirement, a shorter turnaround time for samples, the advantage of being a walk-away technology, and the ability to perform a highly standardized platelet function assessment.

摘要

光传输聚集测定法(LTA)是血小板功能评估的“金标准”,但它既耗时又费力。最近,一种在常规凝血分析仪(Sysmex CS-2100i)上开发的自动化血小板聚集方法已经问世。在这项研究中,评估了 CS-2100i 的性能,包括重复性、与参考聚集仪(Chrono-log Model 700)的相关性,以及富含血小板血浆(PRP)中血小板计数的阈值限制,以用于临床应用。激动剂为二磷酸腺苷(ADP)、花生四烯酸、胶原、肾上腺素和瑞斯托菌素。通过使用血小板减少血浆(PPP)和生理盐水(PS)调整 PRP 中的血小板浓度。CS-2100i 在进行血小板聚集时表现出极好的重复性和与 Chrono-log 700 的强相关性,其 PRP 中血小板计数的阈值限制为 80×10/L。PPP 对 ADP、花生四烯酸、胶原或肾上腺素诱导的血小板聚集有抑制作用;而 PS 对瑞斯托菌素诱导的聚集有抑制作用。对于 ADP、花生四烯酸、胶原或肾上腺素诱导的聚集,应使用 PS 来调整 PRP;而对于瑞斯托菌素诱导的聚集,则推荐使用 PPP。CS-2100i 具有极好的重复性、与 Chrono-log 700 的强相关性、较低的血小板计数要求、较短的样本周转时间、无需人工操作的优势,以及进行高度标准化的血小板功能评估的能力。

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