确定不同血液储存条件对血凝块形成和剪切消化的影响

Alexei Christodoulides, Ziqian Zeng, Abigail R. Hall, Nathan J. Alves
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引用次数: 0

摘要

旨在了解储存对全血(WB)凝结影响的研究通常依赖于描述静态条件下的凝结特征。利用分馏和重组全血(rWB)产品探索生理剪切力对凝块形成和血栓溶解影响的工作很少。将全血分馏为无血小板血浆、包装红细胞和血小板,并在理想条件下(包括血小板冷冻保存)保存每种成分。在 91 天的贮存过程中,它们以各自的原始比例重新组合,并利用血栓弹性成像和钱德勒循环分析凝血/溶栓情况。RWB 可在 91 天内保持凝血强度,与基线的偏差极小,而在 4°C 下贮存的 WB 在贮存第 42 天时凝血强度显著下降。在剪切力作用下,rWB 和 WB 的凝块形成都会导致凝块质量在储存过程中增加。rWB在储存到第70天时与基线相比没有明显偏差。两组的溶栓程度都在增加,其中 rWB 在第 70 天时明显偏离基线。在整个储存和重组过程中,血凝块的整体结构没有发生明显变化。这种分馏和重组方案可作为进一步开发可重复的体外凝块类似物的方法,用于临床前溶栓疗法筛选。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Determining the effects of varying blood storage conditions on clot formation and digestion under shear

Determining the effects of varying blood storage conditions on clot formation and digestion under shear

Studies aiming to understand the effects of storage on whole blood (WB) clotting often rely on characterizing coagulation under static conditions. Minimal work has explored the effects of physiologic shear on clot formation and thrombolysis utilizing fractionated and reconstituted whole blood (rWB) products. WB was fractionated into platelet-free plasma, packed red blood cells, and platelets storing each component under its ideal conditions—including platelet cryopreservation. Recombination at their native ratios was accomplished over 91 days of storage and clotting/thrombolysis was analyzed utilizing thromboelastography and Chandler loop. rWB preserved clot strength through 91 days with minimal deviation from baseline, in contrast to WB stored at 4°C which experienced a significant decline by storage Day-42. Clot formation under shear for both rWB and WB led to increased clot mass through storage. No significant deviation from baseline was appreciated until Day 70 of storage in rWB. Increasing degrees of thrombolysis were seen in both groups, with rWB significantly deviating from baseline at Day 70. No significant changes in overall clot architecture occurred throughout storage and recombination. This fractionation and recombination protocol serves as a method to further develop reproducible in vitro clot analogs for preclinical thrombolytic therapy screening.

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