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用于血液透析期间达肝素抗凝床边监测的活化凝血因子X全血凝固时间(Xa-ACT)

Factor Xa-activated whole blood clotting time (Xa-ACT) for bedside monitoring of dalteparin anticoagulation during haemodialysis.

作者信息

Frank Rolf Dario, Brandenburg Vincent M, Lanzmich Regina, Floege Jürgen

机构信息

Department of Nephrology and Clinical Immunlogy, University Hospital Aachen, D-52057 Aachen, Germany.

出版信息

Nephrol Dial Transplant. 2004 Jun;19(6):1552-8. doi: 10.1093/ndt/gfh203. Epub 2004 Mar 19.

DOI:10.1093/ndt/gfh203
PMID:15034159
Abstract

BACKGROUND

Low molecular weight heparins (LMWH) like dalteparin are increasingly used for anticoagulation during haemodialysis (HD). The available laboratory tests for monitoring LMWH anticoagulation are time-consuming and expensive, and the suitability of the conventional activated clotting time (ACT) is controversial. A simple and cheap bedside test would be useful.

METHODS

We studied the factor Xa-activated whole blood clotting time (Xa-ACT) in vitro and in vivo in nine patients undergoing chronic HD with i.v. dalteparin bolus anticoagulation and compared it with the conventional ACT. Plasma anti-factor Xa (antiXa) activity was determined with a chromogenic assay. Thrombin-antithrombin complexes were measured to detect coagulation activation.

RESULTS

Xa-ACT and ACT were prolonged with rising dalteparin concentration. In vitro, both clotting times were strongly correlated with the antiXa levels (r = 0.94 and 0.89, respectively). Nevertheless, compared with the ACT, the Xa-ACT was considerably more sensitive to the LMWH in vitro (healthy blood: Xa-ACT 90 s/U vs ACT 26 s/U; uraemic blood: Xa-ACT 96 s/U vs ACT 31 s/U) as well as in vivo (Xa-ACT 81 s/U vs ACT 22 s/U) and reflected different intensities of anticoagulation. An initial dalteparin bolus of 80+/-11 U/kg body weight was able to prevent coagulation activation for up to 4 h of HD.

CONCLUSION

For monitoring LMWH anticoagulation the Xa-ACT was superior to the conventional ACT in vitro as well as in vivo during HD. The Xa-ACT can be useful as a LMWH bedside test. The ACT was not sensitive enough to serve as a LMWH monitoring tool.

摘要

背景

低分子量肝素(LMWH)如达肝素在血液透析(HD)期间越来越多地用于抗凝。用于监测LMWH抗凝的现有实验室检测耗时且昂贵,传统活化凝血时间(ACT)的适用性存在争议。一种简单且廉价的床旁检测将很有用。

方法

我们在9例接受静脉注射达肝素推注抗凝的慢性HD患者中,对体外和体内的Xa活化全血凝血时间(Xa-ACT)进行了研究,并将其与传统ACT进行比较。用显色法测定血浆抗Xa因子(抗Xa)活性。测量凝血酶 - 抗凝血酶复合物以检测凝血激活。

结果

随着达肝素浓度升高,Xa-ACT和ACT延长。在体外,两种凝血时间均与抗Xa水平密切相关(分别为r = 0.94和0.89)。然而,与ACT相比,Xa-ACT在体外(健康血液:Xa-ACT 90 s/U vs ACT 26 s/U;尿毒症血液:Xa-ACT 96 s/U vs ACT 31 s/U)以及体内(Xa-ACT 81 s/U vs ACT 22 s/U)对LMWH更为敏感,并反映了不同强度的抗凝作用。初始剂量为80±11 U/kg体重的达肝素推注能够在长达4小时的HD期间预防凝血激活。

结论

在HD期间,对于监测LMWH抗凝,Xa-ACT在体外和体内均优于传统ACT。Xa-ACT可作为LMWH床旁检测。ACT不够敏感,不能用作LMWH监测工具。

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