Harenberg J
Medical University Clinic, Heidelberg, FRG.
J Mal Vasc. 1987;12 Suppl B:68-70.
Heptest, a new one-stage clotting assay was compared with the anti-factor Xa chromogenic substrate S 2222 method, the thrombin clotting time (TCT), and the activated partial thromboplastin time (aPTT) tests in 100 patients receiving unfractionated mucosal heparin, and 100 patients treated with Kabi 2165 low molecular weight heparin. The results indicate a high correlation between the Heptest and the anti-Xa chromogenic substrate method (r = 0.91 for unfractionated heparin, and 0.90 for Kabi 2165 low molecular weight heparin). The correlations between the Heptest and the aPTT were 0.36 for unfractionated heparin, and 0.14 for low molecular weight heparin, while those of the TCT were 0.36 and 0.27, respectively. The test is a very sensitive, simple, highly reproducible and reliable clotting assay for unfractionated and low molecular weight heparins in plasma.
在100例接受普通黏膜肝素治疗的患者和100例接受卡比2165低分子量肝素治疗的患者中,对一种新的一步凝血试验——七因子试验(Heptest)与抗Xa因子显色底物S 2222法、凝血酶凝血时间(TCT)及活化部分凝血活酶时间(aPTT)试验进行了比较。结果表明,七因子试验与抗Xa因子显色底物法之间具有高度相关性(普通肝素组r = 0.91,卡比2165低分子量肝素组r = 0.90)。七因子试验与aPTT之间的相关性,普通肝素组为0.36,低分子量肝素组为0.14;而与TCT之间的相关性分别为0.36和0.27。该试验是一种针对血浆中普通肝素和低分子量肝素的非常灵敏、简单、高度可重复且可靠的凝血试验。