Darlington Daniel N, Kheirabadi Bijan S, Scherer Michael R, Martini Wenjun Z, Dubick Michael A
US Army Institute of Surgical Research Fort Sam Houston, TX 78234, USA.
Int J Burns Trauma. 2012;2(3):145-57. Epub 2012 Dec 5.
Hemorrhagic shock and trauma are associated with acidosis and altered coagulation. A fall in pH has been reported to attenuate the activity of recombinant activated Factor VII (rFVIIa) in vitro. However, it is not known if acidosis induced by hemorrhagic shock or infusion of HCl attenuates FVIIa activity in vivo. The purpose of this study was to determine if acidosis, induced by two methods, affects recombinant FVIIa (rFVIIa) activity in swine, and if correction of the pH restores rFVIIa activity to normal.
Acidosis was induce in anesthetized swine in two separate models: 1) HCl infusion (n=10) and 2) hemorrhage/hypoventilation (n=8). Three groups per model were used: Control (pH7.4), Acidosis (arterial pH7.1) and Acidosis-Corrected (bicarbonate infusion to return pH from 7.1 to 7.4). Pigs were then injected with rFVIIa (90 μg/kg) or vehicle (saline) at target pH and arterial blood samples were taken for measurement of coagulation function, including Thromboelastography -TEG, Thrombin Generation, Activated Clotting Time, Prothrombin Time, activated Partial Thromboplastin Time, Fibrinogen Concentration and Platelet count before and 5min after injection of rFVIIa.
Acidosis led to a hypocoagulation as measured by almost all coagulation parameters in both models. Furthermore, the change in coagulation function produced after infusion of rFVIIa was not different between control, acidosis and acidosis-corrected groups for all coagulation parameters measured.
Acidosis associated with hemorrhagic shock or HCl infusion led to a hypocoagulation that was not corrected with bicarbonate infusion. Furthermore, acidosis did not affect rFVIIa function, and correction of the acidosis with bicarbonate had no effect on rFVIIa function in these models. This suggests that in vivo acidosis did not diminish rFVIIa function.
失血性休克和创伤与酸中毒及凝血功能改变有关。据报道,pH值下降会在体外减弱重组活化凝血因子VII(rFVIIa)的活性。然而,尚不清楚失血性休克或输注盐酸所致的酸中毒是否会在体内减弱FVIIa的活性。本研究的目的是确定两种方法诱导的酸中毒是否会影响猪体内重组FVIIa(rFVIIa)的活性,以及pH值的纠正是否能将rFVIIa活性恢复正常。
在两个不同的模型中对麻醉的猪诱导酸中毒:1)输注盐酸(n = 10)和2)出血/通气不足(n = 8)。每个模型使用三组:对照组(pH7.4)、酸中毒组(动脉pH7.1)和酸中毒纠正组(输注碳酸氢盐使pH从7.1恢复到7.4)。然后在目标pH值下给猪注射rFVIIa(90μg/kg)或赋形剂(生理盐水),并采集动脉血样本以测量凝血功能,包括注射rFVIIa前和注射后5分钟的血栓弹力图(TEG)、凝血酶生成、活化凝血时间、凝血酶原时间、活化部分凝血活酶时间、纤维蛋白原浓度和血小板计数。
在两个模型中,几乎所有凝血参数测量结果均显示酸中毒导致凝血功能减退。此外,对于所有测量的凝血参数,对照组、酸中毒组和酸中毒纠正组在输注rFVIIa后产生的凝血功能变化并无差异。
与失血性休克或输注盐酸相关的酸中毒导致凝血功能减退,输注碳酸氢盐无法纠正。此外,酸中毒不影响rFVIIa功能,在这些模型中用碳酸氢盐纠正酸中毒对rFVIIa功能也无影响。这表明体内酸中毒不会减弱rFVIIa功能。