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戊聚糖那屈肝素抗凝作用的兔模型中凝血酶原复合物浓缩物逆转效果。

Efficacy of prothrombin complex concentrate to reverse the anticoagulant effect of the pentasaccharide fondaparinux in a rabbit model.

机构信息

Department of Anesthesia and Critical Care, Paris Descartes University; Hôtel-Dieu, Paris, France.

出版信息

Thromb Haemost. 2011 Jan;105(1):161-8. doi: 10.1160/TH10-07-0434. Epub 2010 Oct 12.

Abstract

As a potent anticoagulant agent, fondaparinux exposes a risk of bleeding. An effective way to reverse its effects is needed. It was the objective to study efficacy and safety of prothrombin complex concentrate (PCC) to reverse the anticoagulant effect of fondaparinux in a rabbit model of bleeding and thrombosis. In anaesthetised and ventilated rabbits, the Folts model was applied: a stenosis (75%) and an injury were carried out on the carotid artery, inducing thrombosis. Blood flow decreased as thrombus size increased until the pressure gradient was such that the thrombus was released and local blood flow was suddenly restored. This is known as a cyclic flow reduction (CFR). After the first CFR, rabbits were randomised into three groups: control (saline and saline after 1 minute), fondaparinux (fondaparinux [3 mg.kg-1] and saline), PCC (fondaparinux and PCC [40 UI.kg-1]). Then CFRs were recorded over 20 minutes. The following were measured: ear immersion bleeding time (BT), haemoglobin blood level (Hb1) and thrombelastometric parameters (ROTEM®). Finally, a hepatosplenic section was performed; 15 minutes later, the amount of blood loss was recorded as primary endpoint and Hb2 was measured. Blood loss was increased with fondaparinux and normalised with PCC. Regarding ROTEM® INTEM, fondaparinux increased clotting time and clotting formation time. PCC normalised these parameters. EXTEM and FIBTEM tests were not modified. Regarding safety, PCC did not increase CFRs. PCC reduced bleeding without increasing thrombosis and was effective to reverse the haemorrhagic effect of fondaparinux in this rabbit model.

摘要

作为一种有效的抗凝剂,磺达肝素钠会增加出血风险。因此,需要寻找一种有效的逆转其抗凝作用的方法。本研究旨在探讨在兔出血-血栓模型中,应用凝血酶原复合物浓缩物(PCC)逆转磺达肝素钠抗凝作用的疗效和安全性。在麻醉和机械通气的兔子中,应用 Folts 模型:对颈总动脉进行狭窄(75%)和损伤,以诱导血栓形成。随着血栓体积的增加,血流逐渐减少,直至压力梯度使血栓脱落,局部血流突然恢复,即出现周期性血流减少(CFR)。首次出现 CFR 后,兔子随机分为三组:对照组(生理盐水,在 1 分钟后给予生理盐水)、磺达肝素钠组(磺达肝素钠[3mg.kg-1]和生理盐水)、PCC 组(磺达肝素钠和 PCC[40 UI.kg-1])。然后在 20 分钟内记录 CFR。测量以下参数:耳朵浸泡出血时间(BT)、血红蛋白血水平(Hb1)和血栓弹性描记术参数(ROTEM®)。最后,进行肝脾切片,15 分钟后记录失血量作为主要终点,并测量 Hb2。磺达肝素钠组的出血量增加,而 PCC 组可使出血量恢复正常。在 ROTEM®INTEM 中,磺达肝素钠可延长凝血时间和凝血形成时间,而 PCC 可使这些参数恢复正常。EXTEM 和 FIBTEM 测试没有改变。在安全性方面,PCC 未增加 CFR。PCC 减少出血而不增加血栓形成,可有效逆转兔模型中磺达肝素钠的出血作用。

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