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Acidosis and correction of acidosis does not affect rFVIIa function in swine

机译:酸中毒和酸中毒的纠正不影响猪的rFVIIa功能

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Background: 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. Methods: 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. Results: 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. Conclusion: 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.
机译:背景:出血性休克和创伤与酸中毒和凝血改变有关。据报道,pH值的降低会在体外减弱重组活化因子VII(rFVIIa)的活性。但是,尚不清楚由失血性休克或输注HCl引起的酸中毒是否会减弱体内的FVIIa活性。这项研究的目的是确定通过两种方法诱导的酸中毒是否会影响猪中重组FVIIa(rFVIIa)的活性,以及​​pH的校正是否会使rFVIIa的活性恢复正常。方法:在两个独立的模型中,在麻醉的猪中诱发酸中毒:1)输注盐酸(n = 10)和2)出血/换气不足(n = 8)。每个模型使用三组:对照(pH7.4),酸中毒(动脉pH7.1)和酸中毒校正(碳酸氢盐输注,使pH从7.1恢复至7.4)。然后在目标pH值下给猪注射rFVIIa(90μg/ kg)或溶媒(盐水),并采集动脉血样品以测量凝血功能,包括凝血弹性描记法-TEG,凝血酶生成,活化凝血时间,凝血酶原时间,活化部分凝血活酶注射rFVIIa之前和之后5分钟的时间,纤维蛋白原浓度和血小板计数。结果:在两个模型中,几乎所有凝血参数均显示酸中毒导致血凝不足。此外,对于所有测量的凝血参数,在对照组,酸中毒和酸中毒校正组之间,输注rFVIIa后产生的凝血功能变化无差异。结论:酸中毒伴有失血性休克或HCl注入导致低凝,碳酸氢盐注入不能纠正。此外,酸中毒不会影响rFVIIa的功能,在这些模型中,碳酸氢盐对酸中毒的纠正对rFVIIa的功能没有影响。这表明体内酸中毒不会减弱rFVIIa功能。

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