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[Biological monitoring of treatment with low molecular weight heparin].

作者信息

Aiach M, Sié P

机构信息

Laboratoire d'hémostase, Hôpital Broussais, Paris.

出版信息

Ann Biol Clin (Paris). 1988;46(9):715-8.

PMID:2851948
Abstract

The monitoring of low molecular weight heparins (LMWH) can be realized in plasma from treated patients by measuring the anti-Xa activity. The commercially available methods belong to two different categories respectively measuring residual F Xa using clotting or amidolytic methods. The latter may be standardized and provided an appropriate standard is used present acceptable in laboratory variability. These chromogenic substrate based assays have been used in most clinical trial, thus have well known usual ranges. In most cases, it does not seem necessary to perform a biological test in prophylactic treatments. However in curative treatment the anti-Xa activity may help in evaluating the patient sensitivity and allowing a dose adjustment.

摘要

相似文献

1
[Biological monitoring of treatment with low molecular weight heparin].
Ann Biol Clin (Paris). 1988;46(9):715-8.
2
Anti Xa monitoring during treatment with low molecular weight heparin or danaparoid: inter-assay variability.低分子量肝素或达那肝素治疗期间的抗Xa监测:分析间变异性
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Thromb Haemost. 1987 Oct 28;58(3):879-83.
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[Monitoring of plasma concentration of low molecular weight heparin--comparative evaluation with chromogenic and clotting assays].
Rinsho Byori. 1999 Nov;47(11):1046-51.
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Limitations of the chronometric assays to determine plasma antifactor Xa activity during low molecular weight heparin therapy.
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A new chronometric assay to determine plasma antifactor Xa activity which is insensitive to the antithrombin activity of low molecular weight heparins.一种新的计时测定法,用于测定血浆抗Xa因子活性,该方法对低分子量肝素的抗凝血酶活性不敏感。
Nouv Rev Fr Hematol (1978). 1994;35(6):545-9.
10
How useful is the monitoring of (low molecular weight) heparin therapy by anti-Xa assay? A laboratory perspective.通过抗Xa测定监测(低分子量)肝素治疗的实用性如何?实验室视角。
Lab Hematol. 2005;11(3):157-62. doi: 10.1532/LH96.05028.

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BMJ. 1991 Sep 7;303(6802):543-8. doi: 10.1136/bmj.303.6802.543.
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