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首页> 外文期刊>Pharmacology: International Journal of Experimental and Clinical Pharmacology >Assessment of bleeding propensity in non-human primates by combination of selective tissue factor/VIIa inhibition and aspirin compared to warfarin and aspirin treatment.
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Assessment of bleeding propensity in non-human primates by combination of selective tissue factor/VIIa inhibition and aspirin compared to warfarin and aspirin treatment.

机译:与华法林和阿司匹林治疗相比,通过选择性组织因子/ VIIa抑制和阿司匹林的组合评估非人灵长类动物的出血倾向。

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摘要

This study in non-human primates was designed to evaluate the bleeding propensity of a selective, small molecule inhibitor of tissue factor (TF)/VIIa in combination with acetylsalicylic acid (ASA) in comparison to the combination of ASA and warfarin. Bleeding time was increased by ASA but was not prolonged further by the addition of the TF/VIIa inhibitor, PHA-927, at doses that elevated the prothrombin time to 8-fold. In contrast, bleeding time was prolonged by warfarin alone and further exacerbated by the presence of ASA. Acute blood loss at the bleeding site, while not significantly increased by either warfarin or PHA-927, was increased substantially in several individuals treated with a combination of warfarin and ASA but not by the combination of TF/VIIa inhibitor and ASA. These data predict that TF/VIIa inhibition, in the presence of chronic aspirin therapy in patients with cardiovascular risk factors, will be a safe therapy for thrombotic disorders.
机译:这项针对非人类灵长类动物的研究旨在评估与ASA和华法林联合使用的组织因子(TF)/ VIIa选择性小分子抑制剂与乙酰水杨酸(ASA)联合使用时的出血倾向。 ASA可增加出血时间,但添加凝血酶原时间至8倍的TF / VIIa抑制剂PHA-927并不会进一步延长出血时间。相反,单独使用华法令可延长出血时间,而使用ASA则可进一步加剧出血时间。华法林或PHA-927并没有明显增加出血部位的急性失血,但在华法林和ASA联合治疗的几名患者中,出血的急性失血明显增加,但TF / VIIa抑制剂和ASA的联合治疗并未使出血量急剧增加。这些数据预测,在患有心血管危险因素的患者中进行慢性阿司匹林治疗时,TF / VIIa抑制将是治疗血栓形成性疾病的安全方法。

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