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Antithrombin III replacement in animal models of acquired antithrombin III deficiency.

作者信息

Emerson T E

机构信息

Miles, Inc., Pharmaceutical Division, West Haven, CT 06516.

出版信息

Blood Coagul Fibrinolysis. 1994 Jan;5 Suppl 1:S37-45; discussion S59-64. doi: 10.1097/00001721-199401000-00006.

DOI:10.1097/00001721-199401000-00006
PMID:8186355
Abstract

Plasma antithrombin III (AT III) levels decrease early during Gram-negative septicaemia, and even a moderate decrease in this major inhibitor of the coagulation system is associated with serious disseminated intravascular coagulation (DIC). This study reports the efficacy of high dose (at least 250 units/kg) AT III replacement in three animal models of Escherichia coli endotoxaemia or bacteraemia. Highlights of our findings are: 1. Endotoxaemic rat model: DIC occurs early, before the appearance of deleterious cardiovascular abnormalities; AT III prophylaxis attenuates DIC; and AT III prophylaxis increases permanent survival. 2. Endotoxaemic sheep pulmonary dysfunction model: AT III prophylaxis prevents the typical decrease in arterial oxygen partial pressure and AT III prophylaxis combined with alpha 1-proteinase inhibitor significantly attenuates indices of pulmonary dysfunction. 3. E. coli bacteraemic baboon model: AT III prophylaxis and treatment significantly attenuates indices of DIC and organ damage, and prevents death in an otherwise 100% lethal bacterial challenge. In conclusion, prophylactic treatment with high doses of AT III may be efficacious in disease states of impending DIC such as Gram-negative septicaemia. Data presented herein demonstrate that plasma levels of AT III must be maintained at levels markedly higher than normal to be efficacious in animal models of Gram-negative endotoxaemia or bacteraemia.

摘要

相似文献

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Antithrombin III replacement in animal models of acquired antithrombin III deficiency.
Blood Coagul Fibrinolysis. 1994 Jan;5 Suppl 1:S37-45; discussion S59-64. doi: 10.1097/00001721-199401000-00006.
2
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