Loss of factor VIII and von Willebrand factor activities during cold storage of whole blood is reversed by rewarming.

Majed A Refaai, Elisabeth M Van Cott, Michael Lukoszyk, James Hughes, Charles S Eby
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引用次数: 22

Abstract

Documentation of preanalytical conditions that could result in inaccurate results and misdiagnoses of patients is important. It has recently been reported that a significant loss of factor VIII (FVIII) and von Willebrand factor (vWF) activity occurs when citrated whole blood is stored on ice. We tested the hypothesis that the cold-dependent loss of FVIII and vWF activity is due to the formation of cryoprecipitate and is reversed by rewarming the citrated whole blood before centrifugation and removal of plasma. We collected venous blood from 10 healthy subjects into 3.2% sodium citrate glass tubes. One tube was immediately centrifuged and the plasma was stored at -20 degrees C. Following storage in an ice bath (4 degrees C) for 3.5 hours, 1 tube was immediately centrifuged and processed while the second tube was placed in a 37 degrees C water bath for 5 minutes then centrifuged and processed. Subsequently, plasma samples were quickly thawed at 37 degrees C and the following tests were performed: prothrombin time (PT), partial thrombin time (aPTT), FVIII activity, vWF antigen (vWF:Ag), and vWF activity (vWF:Act). Means for each analyte from the 2 tubes stored at 4 degrees C for 3.5 hours with or without rewarming were compared to baseline tube using the Student t test. Compared to the baseline tube results, PT and aPTT showed no significant changes in either of the tubes stored at 4 degrees C for 3.5 hours. However, FVIII, vWF:Ag, and vWF:Act were significantly lower in the tubes stored at 4 degrees C for 3.5 hours, but no differences were detected between baseline and rewarmed tube results. In conclusion, prolonged storage of citrated whole blood at 4 degrees C causes a clinically significant reduction of FVIII and vWF activities. The losses are completely reversed by rewarming the tube prior to processing. This is consistent with a reversible cryoprecipitation of vWF and FVIII rather than a cold-activated enzymatic degradation.

在全血冷藏过程中,因子VIII和血管性血友病因子活性的丧失可通过复温得到逆转。
可能导致不准确结果和误诊患者的分析前条件的记录是重要的。最近有报道称,当柠檬酸全血在冰上储存时,会发生因子VIII (FVIII)和血管性血友病因子(vWF)活性的显著丧失。我们验证了一个假设,即FVIII和vWF活性的冷依赖性损失是由于低温沉淀的形成,并通过在离心和去除血浆之前重新加热柠檬酸全血来逆转。在3.2%柠檬酸钠玻璃管中采集10例健康受试者静脉血。1管立即离心,-20℃保存,4℃冰浴3.5小时后,1管立即离心处理,2管37℃水浴5分钟离心处理。随后,血浆样品在37℃下快速解冻,进行以下测试:凝血酶原时间(PT)、部分凝血酶时间(aPTT)、FVIII活性、vWF抗原(vWF:Ag)和vWF活性(vWF:Act)。使用学生t检验将在4摄氏度下储存或不重新加热3.5小时的2支试管中的每种分析物的平均值与基线试管进行比较。与基线试管结果相比,PT和aPTT在4℃储存3.5小时的试管中均未显示显着变化。然而,在4℃保存3.5小时的试管中,FVIII、vWF:Ag和vWF:Act显著降低,但在基线和重新加热的试管结果之间没有发现差异。综上所述,在4℃下长期储存柠檬酸全血会导致FVIII和vWF活性在临床上显著降低。通过在加工前重新加热管,损耗完全逆转。这与vWF和FVIII的可逆低温沉淀相一致,而不是冷激活的酶降解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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