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重组血小板因子4对人体肝素抗凝作用的逆转

Reversal of heparin anticoagulation by recombinant platelet factor 4 in humans.

作者信息

Dehmer G J, Fisher M, Tate D A, Teo S, Bonnem E M

机构信息

C.V. Richardson Cardiac Catheterization Laboratory, University of North Carolina Hospital, Chapel Hill 27514, USA.

出版信息

Circulation. 1995 Apr 15;91(8):2188-94. doi: 10.1161/01.cir.91.8.2188.

Abstract

BACKGROUND

Protamine is used to reverse the anticoagulant effects of heparin, but it can have important side effects. Platelet factor 4 (PF4) is a protein found in platelet alpha granules that binds to and thereby neutralizes heparin. We evaluated the safety and effectiveness of intravenous recombinant PF4 to neutralize heparin anticoagulation after cardiac catheterization in a phase 1, open-label trial.

METHODS AND RESULTS

The study group consisted of 18 patients having diagnostic cardiac catheterization. Heparin (5000 U) was given after vascular access was obtained. In the first 12 patients, additional heparin was given at the conclusion of the procedure so that all patients had activated coagulation times > 300 seconds before rPF4 was given. Three patients each received 0.5, 1.0, 2.5, or 5.0 mg/kg rPF4 over a period of 3 minutes at the conclusion of the catheterization procedure. In 6 additional patients, extra heparin was not given at the conclusion of the procedure, and 1.0 mg/kg rPF4 was given. Hemodynamic measurements, cardiac output, and serial blood tests were performed 5, 10, 20, and 30 minutes after rPF4 and then into the next 24 hours. There were no serious side effects in any patient, despite transient rPF4 levels as high as 14,870 ng/mL in the patients receiving 5.0 mg/kg. One patient receiving 2.5 mg/kg had a slight transient rise in liver enzymes possibly related to the rPF4. There were no important hemodynamic effects of rPF4 administration at any dose used. Doses of 2.5 and 5.0 mg/kg were uniformly effective in reversing the anticoagulant effect of heparin. At lower doses, rPF4 neutralized the effects of heparin in most but not all patients. Pharmacokinetic analysis suggested a monophasic and one-compartment clearance of the PF4-heparin complex. No neutralizing factors to rPF4 were detected in the samples collected 7 days after dosing.

CONCLUSIONS

rPF4, in doses ranging from 0.5 to 5.0 mg/kg over 3 minutes, had no serious side effects. Given in sufficient amounts, rPF4 can completely and rapidly reverse the anticoagulant effects of heparin.

摘要

背景

鱼精蛋白用于逆转肝素的抗凝作用,但它可能有重要的副作用。血小板因子4(PF4)是一种存在于血小板α颗粒中的蛋白质,它能与肝素结合并使其失活。在一项1期开放标签试验中,我们评估了静脉注射重组PF4在心脏导管插入术后中和肝素抗凝作用的安全性和有效性。

方法与结果

研究组由18例接受诊断性心脏导管插入术的患者组成。在获得血管通路后给予肝素(5000 U)。在前12例患者中,在手术结束时给予额外的肝素,以便所有患者在给予rPF4之前活化凝血时间>300秒。3例患者在导管插入术结束时在3分钟内分别接受0.5、1.0、2.5或5.0 mg/kg的rPF4。在另外6例患者中,手术结束时未给予额外的肝素,并给予1.0 mg/kg的rPF4。在给予rPF4后5、10、20和30分钟,然后持续到接下来的24小时内进行血流动力学测量、心输出量和系列血液检测。尽管接受5.0 mg/kg的患者中rPF4水平短暂高达14,870 ng/mL,但所有患者均未出现严重副作用。1例接受2.5 mg/kg的患者肝酶有轻微短暂升高,可能与rPF4有关。在使用的任何剂量下,给予rPF4均未产生重要的血流动力学影响。2.5和5.0 mg/kg的剂量均能有效逆转肝素的抗凝作用。在较低剂量下,rPF4能使大多数但不是所有患者的肝素作用失活。药代动力学分析表明PF4-肝素复合物呈单相一室清除。给药7天后采集的样本中未检测到rPF4的中和因子。

结论

在3分钟内给予0.5至5.0 mg/kg剂量的rPF4无严重副作用。给予足够剂量时,rPF4能完全且迅速地逆转肝素的抗凝作用。

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