1st Department of Anesthesiology, Medical School, University of Athens, Aretaieio Hospital, Athens, Greece.
J Surg Res. 2011 May 1;167(1):125-30. doi: 10.1016/j.jss.2009.07.037. Epub 2009 Aug 26.
Hypothermia has a detrimental effect on hemostatic mechanism. The purpose of this experimental study was to investigate the effect of graded hypothermia on markers of the anticoagulant system (antithrombin III and protein C) and fibrinolytic system (plasminogen, α(2)-antiplasmin), and on vascular wall and other tissue specimens.
Ten New Zealand rabbits were subjected to mild and then moderate core hypothermia of 32 °C for 60 min. Blood samples were obtained at normothermic (T(1)), mild (T(2)), and moderate (T(3)) hypothermic conditions. Chromogenic assay methods were used to determine quantitatively (%) the activity of antithrombin III, protein C, plasminogen, and α(2)-antiplasmin. Hypothermic values were compared with the normothermic values. Tissue and vessel wall specimens were examined under light microscope.
Reduction of activity (%) from normothermia (T(1)) to mild (T(2)) and moderate (T(3)) hypothermia was found for antithrombin III (103.40 ± 12.54, 87.40 ± 13.50, and 82.70 ± 20.78, respectively, with statistically significant difference between T(1)-T(3): P = 0.03), for protein C (70.1 ± 7.51, 56.30 ± 8.34, and 53.1 ± 7.34, with statistically significant difference between T(1)-T(2) and T(1)-T(3): P = 0.015 for both comparisons) and α(2)-antiplasmin (97 ± 9.63, 80.60 ± 11.73, and 83.70 ± 13.94, with statistically significant difference between T(1)-T(2): P = 0.006). Plasminogen activity was increased (14.50 ± 0.52, 16.30 ± 1.63, and 17.30 ± 2.45, with statistically significant difference between T(1)-T(2) and T(1)-T(3): P = 0.033 for both comparisons). Histologic examination revealed no significant lesions on tissue and vessel wall specimens.
The results of our study suggest that even though the hypothermia period was relatively short, the processes of coagulation and fibrinolysis were altered with simultaneous changes.
低温对止血机制有不利影响。本实验研究的目的是探讨不同程度的低温对抗凝系统标志物(抗凝血酶 III 和蛋白 C)和纤溶系统标志物(纤溶酶原、α(2)-抗纤溶酶)以及血管壁和其他组织标本的影响。
10 只新西兰兔先接受 32°C 的轻度和中度核心低温 60 分钟。在正常体温(T(1))、轻度(T(2))和中度(T(3))低温条件下采集血液样本。采用显色法测定抗凝血酶 III、蛋白 C、纤溶酶原和α(2)-抗纤溶酶的活性(%)。将低温值与正常体温值进行比较。用显微镜检查组织和血管壁标本。
与正常体温(T(1))相比,轻度(T(2))和中度(T(3))低温时,抗凝血酶 III(分别为 103.40±12.54、87.40±13.50 和 82.70±20.78,T(1)-T(3) 之间差异有统计学意义:P=0.03)、蛋白 C(分别为 70.1±7.51、56.30±8.34 和 53.1±7.34,T(1)-T(2)和 T(1)-T(3)之间差异有统计学意义:两者比较均 P=0.015)和α(2)-抗纤溶酶(分别为 97±9.63、80.60±11.73 和 83.70±13.94,T(1)-T(2) 之间差异有统计学意义:P=0.006)的活性降低。纤溶酶原活性升高(分别为 14.50±0.52、16.30±1.63 和 17.30±2.45,T(1)-T(2)和 T(1)-T(3)之间差异有统计学意义:两者比较均 P=0.033)。组织和血管壁标本的组织学检查未见明显病变。
本研究结果表明,即使低温期相对较短,凝血和纤溶过程也会发生改变,同时发生变化。