血小板-白细胞复合物的增加不会导致血小板球蛋白捐献者的凝血活化。

Fatih Tastekin, Olga Meltem Akay, Ertugrul Colak, Eren Gunduz
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引用次数: 0

摘要

背景:尽管血小板捐献被普遍认为是一种安全的程序,但其对血小板功能、凝血系统和纤溶的影响尚未完全阐明:研究设计:前瞻性观察研究:研究设计:前瞻性观察研究:我们使用流式细胞术测定血小板-单核细胞复合物(PMC)和血小板-中性粒细胞复合物(PNC)的水平:结果:血小板-中性粒细胞复合物(PNC)水平在抽血七天后明显升高,与刚抽血后和抽血 24 小时后相比(P 0.05)。PF1+2的水平在血小板穿刺后立即比穿刺前明显降低(P 结论:血小板穿刺影响了血液中的PMC水平:我们得出的结论是,血小板分离会影响血小板活化,但不会导致凝血活化发生任何变化。
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Increased platelet-leucocyte complexes do not result in coagulation activation in plateletpheresis donors.

Background: Although plateletpheresis donation is commonly accepted as a safe procedure, its influence on platelet function, coagulation system and fibrinolysis is not completely elucidated.

Objectives: In this study, we tried to assess the effects of plateletpheresis on donor's hemostasis system by measuring platelet activation, development of platelet-leukocyte aggregates, and coagulation activation.

Study design: Prospective observational study.

Methods: We used flow cytometry to determine the levels of platelet-monocyte complexes (PMC) and platelet-neutrophil complexes (PNC). sP-selectin and prothrombin fragment (PF) 1 + 2 values were determined by ELISA.

Results: The PMC levels increased significantly seven days after apheresis in comparison with just after apheresis and 24 h after apheresis (p < 0.05). The PNC levels increased significantly seven days after apheresis compared to immediately after apheresis (p < 0.05). sP-selectin values decreased significantly immediately after apheresis (p < 0.05). While sP-selectin values increased seven days after apheresis in comparison with immediately after apheresis and 24 h after apheresis, but there were not statistically significant differences for sP-selectin levels (p > 0.05). PF1 + 2 levels decreased significantly immediately after apheresis compared to pre-apheresis (p < 0.05) and increased 24 h after apheresis and seven days after apheresis, but these differences were not statistically significant.

Conclusion: We concluded that plateletpheresis affects platelet activation but does not cause any change in coagulation activation.

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