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肝素与血浆蛋白结合,这是肝素抵抗的一个重要机制。

Heparin binding to plasma proteins, an important mechanism for heparin resistance.

作者信息

Young E, Prins M, Levine M N, Hirsh J

机构信息

Department of Pathology, McMaster University, Hamilton, Canada.

出版信息

Thromb Haemost. 1992 Jun 1;67(6):639-43.

PMID:1509402
Abstract

Heparin dosage requirements vary widely among patients with venous thromboembolism. In this study, we measured the proportion of anticoagulantly-active heparin which was reversibly bound and neutralized by plasma proteins (defined as reversible heparin neutralization) in the pre-treatment plasma (in vitro) and in the 6 h post-treatment plasma (ex vivo) of patients with venous thromboembolism treated with a fixed dose of heparin. Reversible heparin neutralization was assessed by comparing the heparin levels measured as anti-factor Xa activity before and after the addition of low affinity heparin which is essentially devoid of anti-factor Xa activity, in order to displace heparin bound to plasma proteins. The results indicate that reversible heparin neutralization due to binding to plasma proteins is a major determinant of the anticoagulant response to a fixed dose of standard heparin 6 h post-treatment and of the eventual heparin dose required to achieve a therapeutic anticoagulant effect on days 3-5 of heparin treatment.

摘要

静脉血栓栓塞患者的肝素剂量需求差异很大。在本研究中,我们测定了接受固定剂量肝素治疗的静脉血栓栓塞患者治疗前血浆(体外)和治疗后6小时血浆(体内)中与血浆蛋白可逆结合并被中和的抗凝活性肝素比例(定义为可逆性肝素中和)。通过比较添加基本无抗Xa因子活性的低亲和力肝素前后以抗Xa因子活性测定的肝素水平来评估可逆性肝素中和,以便置换与血浆蛋白结合的肝素。结果表明,与血浆蛋白结合导致的可逆性肝素中和是治疗后6小时对固定剂量标准肝素抗凝反应的主要决定因素,也是肝素治疗第3 - 5天达到治疗性抗凝效果所需最终肝素剂量的主要决定因素。

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