Heparin Binding to Plasma Proteins, an Important Mechanism for Heparin Resistance

Author:

Young Edward1,Prins Martin2,Levine Mark N23,Hirsh Jack2

Affiliation:

1. The Department of Pathology, McMaster University, and the Hamilton Civic Hospitals Research Centre, Hamilton, Canada

2. The Department of Medicine, McMaster University, and the Hamilton Civic Hospitals Research Centre, Hamilton, Canada

3. The Department of Clinical Epidemiology and Biostatistics, McMaster University, and the Hamilton Civic Hospitals Research Centre, Hamilton, Canada

Abstract

SummaryHeparin 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 antifactor 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.

Publisher

Georg Thieme Verlag KG

Subject

Hematology

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