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接受冠状动脉介入治疗患者的肝素剂量

Heparin dosing in patients undergoing coronary intervention.

作者信息

Popma J J, Prpic R, Lansky A J, Piana R

机构信息

Department of Internal Medicine, the Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Am J Cardiol. 1998 Oct 22;82(8B):19P-24P. doi: 10.1016/s0002-9149(98)00759-0.

Abstract

Unfractionated heparin remains an essential component of the antithrombotic regimen in patients undergoing coronary intervention, although the timing, dosing, and duration of heparin therapy have evolved over the past several years. Complications associated with heparin use include bleeding events, which occur in 3.9-16.4% of patients receiving conventional heparin. Less commonly, clinically significant thrombocytopenia develops, related to the duration of heparin administration. In patients undergoing coronary intervention who do not receive platelet glycoprotein (GP) IIb/IIIa inhibitors, sufficient heparin should be given to achieve an activated clotting time (ACT) of 250-300 seconds with the HemoTec device and 300-350 seconds with the Hemochron device. There is a general trend to use lower, weight-adjusted heparin dosing (70-100 units/kg) to avoid excessive levels of anticoagulation, with additional heparin boluses to achieve a therapeutic ACT level. When GP IIb/IIIa inhibitors are used, weight-adjusted heparin dosing can be decreased to 70 units/kg to achieve a target ACT of 200 seconds with either the HemoTec or Hemochron device. After uncomplicated coronary intervention, there appears to be little value associated with continued heparin therapy, and the risk of bleeding complications clearly increases with longer durations and higher levels of anticoagulation after coronary intervention.

摘要

普通肝素仍然是接受冠状动脉介入治疗患者抗栓治疗方案的重要组成部分,尽管在过去几年中肝素治疗的时机、剂量和持续时间已经有所发展。与肝素使用相关的并发症包括出血事件,在接受传统肝素治疗的患者中,出血事件发生率为3.9%-16.4%。较少见的是,与肝素给药持续时间相关的具有临床意义的血小板减少症会发生。在未接受血小板糖蛋白(GP)IIb/IIIa抑制剂的冠状动脉介入治疗患者中,应给予足够的肝素,使用HemoTec装置时使活化凝血时间(ACT)达到250-300秒,使用Hemochron装置时达到300-350秒。目前普遍倾向于使用较低的、根据体重调整的肝素剂量(70-100单位/千克)以避免过度抗凝,并给予额外的肝素推注以达到治疗性ACT水平。当使用GP IIb/IIIa抑制剂时,根据体重调整的肝素剂量可降至70单位/千克,使用HemoTec或Hemochron装置时使目标ACT达到200秒。在无并发症的冠状动脉介入治疗后,继续肝素治疗似乎没有什么价值,并且冠状动脉介入治疗后抗凝持续时间延长和水平升高会明显增加出血并发症的风险。

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