Enoxaparin and percutaneous coronary intervention: a Canadian perspective.

The Canadian journal of cardiology Pub Date : 2005-05-01
David Fitchett, Robert Welsh, Anatoly Langer, Shaun Goodman
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Abstract

Background: The low molecular weight heparin enoxaparin is commonly used in the management of patients with non-ST segment elevation acute coronary syndromes (ACS). It is perceived that there is variable acceptance of the use of enoxaparin in patients with ACS in conjunction with percutaneous coronary intervention (PCI) by Canadian interventional cardiologists, as well as diverse approaches to the procedural (ie, PCI) management of anticoagulation.

Methods and results: A survey assessing physician and centre demographics, as well as the opinion and approach to the use of enoxaparin in patients undergoing PCI, was developed. All 141 interventional cardiologists performing PCI in Canada were sent the survey, with a 52% response rate. The majority (64%) of respondents were comfortable performing PCI during enoxaparin treatment, but almost one-half (46.5%) stated a preference to have a point-of-care measurement of the anticoagulation level during the procedure. Various 'top-up' protocols are used across the country, including fixed-dose intravenous (IV) enoxaparin, weight-adjusted IV enoxaparin, fixed-dose IV unfractionated heparin, weight-adjusted IV unfractionated heparin and IV unfractionated heparin titrated to a target activated clotting time. Although the median time threshold for administering a 'top-up' dose of anticoagulation matched current recommendations, there was a wide variation ranging from 2 h to 10 h (median 8 h).

Conclusions: Although the majority of Canadian interventional cardiologists were comfortable performing PCI in patients treated with enoxaparin, the survey demonstrated various levels of confidence and a diverse range of 'top-up' anticoagulation procedures. Nationwide guidelines for the management of anticoagulation in patients with ACS undergoing PCI with enoxaparin should be developed from the best available clinical and research evidence to limit potential patient risk of inadequate or excessive anticoagulation. This is especially relevant in view of the association between switching among anticoagulant therapies and an increased bleeding risk in patients undergoing early cardiac catheterization and PCI that was found in the recently reported Superior Yield of the New Strategy of Enoxaparin, Revascularization and Glycoprotein IIb/IIIa Inhibitors (SYNERGY) trial.

依诺肝素和经皮冠状动脉介入治疗:加拿大的观点。
背景:低分子肝素依诺肝素常用于非st段抬高急性冠脉综合征(ACS)患者的治疗。加拿大介入心脏病专家认为,ACS患者联合经皮冠状动脉介入治疗(PCI)使用依诺肝素的接受程度不一,抗凝治疗的程序性(即PCI)管理方法也多种多样。方法和结果:一项评估医生和中心人口统计数据的调查,以及在接受PCI的患者中使用依诺肝素的意见和方法。所有141名在加拿大实施PCI的介入心脏病专家都接受了调查,回复率为52%。大多数(64%)受访者在依诺肝素治疗期间接受PCI治疗,但几乎一半(46.5%)的受访者表示更倾向于在治疗过程中进行即时抗凝水平测量。全国各地都在使用各种“补充”方案,包括固定剂量静脉注射(IV)依诺肝素、体重调整型静脉注射依诺肝素、固定剂量静脉注射无分离肝素、体重调整型静脉注射无分离肝素和滴定到靶活化凝血时间的静脉注射无分离肝素。虽然给予“补充”剂量抗凝治疗的中位时间阈值与目前的推荐值相匹配,但从2小时到10小时(中位8小时)的范围变化很大。结论:尽管大多数加拿大介入心脏病专家对接受依诺肝素治疗的患者进行PCI治疗感到满意,但调查显示了不同程度的信心和不同范围的“补充”抗凝治疗。全国范围内的ACS患者抗凝治疗指南应根据现有的最佳临床和研究证据制定,以限制患者抗凝治疗不足或过度的潜在风险。最近报道的依诺肝素、血运重建和糖蛋白IIb/IIIa抑制剂新策略(SYNERGY)试验发现,抗凝治疗之间的切换与早期心导管和PCI患者出血风险增加之间的关联尤其重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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