Ts'ao C, Swedlund J, Neofotistos D
Department of Pathology, Northwestern Memorial Hospital, Chicago, Ill.
Arch Pathol Lab Med. 1994 Dec;118(12):1183-7.
The recent introduction of thromboplastin reagents with low international sensitivity index (ISI) values into the US market for the purpose of generating a more precise international normalized ratio than high ISI thromboplastins could has necessitated an evaluation of the impact of the low ISI reagents on prothrombin time (PT) testing in general. In this study, PT testing with three thromboplastin reagents, one of which (presently used in our laboratory) has an ISI of 2.10 and the other two ISI values of 0.92 and 1.06, respectively, was performed on normal individuals, on quality control reference plasma specimens and single-factor-deficient plasma specimens, and on patients with liver disease, intravascular coagulation, and receiving oral anticoagulant therapy. We found that PTs of normal individuals determined by all three thromboplastins were virtually identical. The thromboplastins with a low ISI generated much longer PTs on abnormal reference plasma specimens than did the high ISI product. Low ISI reagents also produced longer PTs in all three groups of patients. However, the degree of prolongation was far greater for patients receiving warfarin than for the other two groups of patients. Conversion of the PT to an international normalized ratio minimized the discrepancy seen in the PT ratio in patients receiving oral anticoagulants. The two low ISI thromboplastins did not produce near-identical values of PT, PT ratio, or international normalized ratio on plasma specimens obtained from patients who received warfarin therapy. The critical value set for PT with a high ISI thromboplastin would not be adequate if the reagent is to be replaced with a low ISI product.
近期,国际敏感度指数(ISI)值较低的凝血活酶试剂进入美国市场,目的是生成比高ISI凝血活酶更精确的国际标准化比值,这就需要总体评估低ISI试剂对凝血酶原时间(PT)检测的影响。在本研究中,使用三种凝血活酶试剂对正常个体、质量控制参考血浆标本和单因子缺乏血浆标本,以及肝病、血管内凝血和接受口服抗凝治疗的患者进行PT检测。其中一种试剂(目前在我们实验室使用)的ISI为2.10,另外两种试剂的ISI值分别为0.92和1.06。我们发现,由所有三种凝血活酶测定的正常个体的PT实际上是相同的。低ISI的凝血活酶在异常参考血浆标本上产生的PT比高ISI产品长得多。低ISI试剂在所有三组患者中也产生了更长的PT。然而,接受华法林治疗的患者的延长程度远大于其他两组患者。将PT转换为国际标准化比值可最大限度地减少接受口服抗凝剂治疗患者的PT比值差异。两种低ISI凝血活酶在接受华法林治疗患者的血浆标本上产生的PT、PT比值或国际标准化比值并不接近相同。如果要用低ISI产品替代高ISI凝血活酶试剂,那么为高ISI凝血活酶设定的PT临界值将不够用。