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自体凝血酶:术中由全血制备。

Autologous thrombin: intraoperative production from whole blood.

作者信息

Kumar Vijay, Chapman John R

机构信息

Thermogenesis Corporation, Rancho Cordova, California 95742, USA.

出版信息

J Extra Corpor Technol. 2008 Jun;40(2):94-8.

Abstract

Thrombin is routinely combined in surgical practice with a fibrinogen source to prepare fibrin sealant to promote hemostasis or with platelet concentrates to prepare platelet gels to enhance wound healing. The purpose of this study was to evaluate the robustness and reproducibility of a new sterile handheld disposable thrombin-processing device (TPD) to generate autologous human thrombin in the intraoperative setting, using whole blood as the starting source material. By using whole blood instead of plasma as the starting material, it is possible to eliminate the plasma separation step from whole blood and reduce the thrombin production time and increase its availability to the surgical team intraoperatively. Active thrombin was prepared by combining 4 mL of thrombin reagent (a mixture of calcium chloride and ethanol) to 11 mL of blood in a reaction chamber containing negatively charged particles. The whole blood, reagent and particle mixture was incubated for 25 minutes at either 18 degrees C or 24 degrees C (n = 25/group) to assess stability of the thrombin activity. The mean activity of the thrombin produced at 18 degrees C and 24 degrees C was 52 +/- 14 (n = 25) and 61 +/- 12.2 IU/mL (n = 25), respectively. The average volume of thrombin harvested from each aliquot of blood at 18 degrees C and 24 degrees C was 10 +/- 0.4 and 9 +/- 0.6 mL, respectively. The thrombin concentration generated was shown to rapidly (<5 seconds) coagulate fibrinogen concentrate and retained clotting activity for 1 hour at room temperature (18-26 degrees C) and up to 4 hours when stored on ice. The results show that the TPD is able to consistently generate high thrombin activity from human whole blood. The device offers a robust and rapid approach for preparing active thrombin from whole blood.

摘要

在外科手术中,凝血酶通常与纤维蛋白原来源联合使用以制备纤维蛋白密封剂来促进止血,或者与血小板浓缩物联合使用以制备血小板凝胶来促进伤口愈合。本研究的目的是评估一种新型无菌手持式一次性凝血酶处理装置(TPD)在术中使用全血作为起始原料生成自体人凝血酶的稳健性和可重复性。通过使用全血而非血浆作为起始原料,可以省去从全血中分离血浆的步骤,减少凝血酶的生产时间,并增加其在术中对外科团队的可用性。在含有带负电荷颗粒的反应室中,将4 mL凝血酶试剂(氯化钙和乙醇的混合物)与11 mL血液混合来制备活性凝血酶。将全血、试剂和颗粒混合物在18℃或24℃下孵育25分钟(每组n = 25),以评估凝血酶活性的稳定性。在18℃和24℃下产生的凝血酶的平均活性分别为52±14(n = 25)和61±12.2 IU/mL(n = 25)。在18℃和24℃下,从每份血液等分试样中收获的凝血酶平均体积分别为10±0.4 mL和9±0.6 mL。所产生的凝血酶浓度显示能使纤维蛋白原浓缩物迅速(<5秒)凝固,并在室温(18 - 26℃)下保持凝血活性1小时,在冰上储存时可达4小时。结果表明,TPD能够从人全血中持续产生高凝血酶活性。该装置为从全血中制备活性凝血酶提供了一种稳健且快速的方法。

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