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抗凝血酶缺乏患者的肝素监测。

Monitoring of heparins in antithrombin-deficient patients.

机构信息

Department of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands; Department of Haematology, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.

Department of Laboratory Medicine, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.

出版信息

Thromb Res. 2019 Mar;175:8-12. doi: 10.1016/j.thromres.2019.01.007. Epub 2019 Jan 15.

Abstract

INTRODUCTION

Heparins exert their anticoagulant effect through activation of antithrombin. Whether antithrombin deficiency leads to clinically relevantly reduced anti-Xa activity of heparins is unknown. We investigated the relation between antithrombin deficiency and anti-Xa activity measurements of plasma samples spiked with unfractionated heparin (UFH) or low-molecular-weight heparin (LMWH).

MATERIALS AND METHODS

Plasma samples from 34 antithrombin-deficient subjects and 17 family controls were spiked with UFH and LMWH (nadroparin) aimed to correspond with an anti-Xa activity of 0.8 IU/mL. Antithrombin, β-antithrombin and anti-Xa activities were measured.

RESULTS

Mean anti-Xa activity with LWMH was 0.55 IU/mL (0.30-0.74) (recovery 69%, 38-93%) in antithrombin-deficient subjects and 0.82 (0.71-0.89) IU/mL in controls (recovery 103%, 89-111%). Expected anti-Xa measurements after LMWH spiking were found in 17/17 non-deficient subjects and in 8/34 antithrombin-deficient subjects. Anti-Xa measurements in the expected range (0.6-1.0 IU/mL) after UFH spiking were found in 17/17 non-deficient subjects and in 1/22 antithrombin-deficient subjects. Antithrombin activity correlated with anti-Xa activity of UFH (R = 0.77) and LMWH (R = 0.66). Mixing studies of pooled normal plasma and antithrombin-deficient plasma showed that anti-Xa recovery was linearly reduced with antithrombin activity decreasing below 100%.

CONCLUSIONS

Reduced antithrombin activity causes significantly reduced anti-Xa levels. Standard LWMH- or UFH-doses are likely to lead to under treatment in antithrombin-deficient individuals.

摘要

简介

肝素通过激活抗凝血酶发挥其抗凝作用。抗凝血酶缺乏是否会导致肝素的抗 Xa 活性显著降低尚不清楚。我们研究了抗凝血酶缺乏与普通肝素(UFH)或低分子肝素(LMWH)(那屈肝素)加样后的血浆样本抗 Xa 活性测量之间的关系。

材料和方法

从 34 名抗凝血酶缺乏的受试者和 17 名家族对照者的血浆样本中加样 UFH 和 LMWH(那屈肝素),以达到 0.8 IU/mL 的抗 Xa 活性。测量抗凝血酶、β-抗凝血酶和抗 Xa 活性。

结果

LMWH 加样后,抗凝血酶缺乏者的平均抗 Xa 活性为 0.55 IU/mL(0.30-0.74)(回收率 69%,38-93%),对照组为 0.82 IU/mL(0.71-0.89)(回收率 103%,89-111%)。在 17 名非缺乏受试者和 8 名抗凝血酶缺乏受试者中发现了预期的 LMWH 加样后的抗 Xa 测量值。在 UFH 加样后,在 17 名非缺乏受试者和 1 名抗凝血酶缺乏受试者中发现了预期范围内(0.6-1.0 IU/mL)的抗 Xa 测量值。UFH 和 LMWH 的抗 Xa 活性与抗凝血酶活性呈正相关(R=0.77 和 R=0.66)。混合正常血浆和抗凝血酶缺乏血浆的研究表明,随着抗凝血酶活性降低至 100%以下,抗 Xa 回收率呈线性降低。

结论

抗凝血酶活性降低导致抗 Xa 水平显著降低。标准 LMWH 或 UFH 剂量可能导致抗凝血酶缺乏的个体治疗不足。

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