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活化部分凝血活酶时间试剂:一项评估。

Activated partial thromboplastin time reagents: an evaluation.

作者信息

Howarth S

机构信息

Department of Pathology, King Edward Memorial Hospital for Women, Subiaco, Perth, Western Australia.

出版信息

Br J Biomed Sci. 1993 Jun;50(2):109-13.

PMID:8219915
Abstract

Nine automated, activated partial thromboplastin time (APTT) reagents were evaluated on an automated coagulometer, in comparison with a manual reagent. The study consisted of three separate stages: 1) to choose a reagent that had a working stability between 4 degrees C and 8 degrees C for seven days and heparin sensitivity between 0 and 0.8 iu/ml; ii) assessment of sensitivity to specific factor deficiencies, particularly factors VIII, IX, XI and XII using standardised plasma serially diluted with factor-deficient plasma; and iii) assessment of sensitivity to the presence of a lupus anticoagulant, from a known positive panel. Only one reagent fulfilled all the essential criteria as an acceptable replacement for the manual reagent.

摘要

在自动凝血仪上对九种自动化活化部分凝血活酶时间(APTT)试剂进行了评估,并与一种手工试剂进行了比较。该研究包括三个独立阶段:1)选择一种在4摄氏度至8摄氏度之间工作稳定性为七天且肝素敏感性在0至0.8国际单位/毫升之间的试剂;ii)使用用缺乏因子的血浆连续稀释的标准化血浆评估对特定因子缺乏的敏感性,特别是因子VIII、IX、XI和XII;iii)从已知阳性样本中评估对狼疮抗凝物存在的敏感性。只有一种试剂满足了作为手工试剂可接受替代品的所有基本标准。

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