Conkie J A, McCall F, Walker I D, Davidson J F
Haemostasis. 1984;14(4):307-11. doi: 10.1159/000215080.
The performance of a commercially available assay for the determination of prothrombin by a chromogenic substrate method has been evaluated for use on an automated clinical analyser. The method was rapid and simple; accuracy, precision and sensitivity were satisfactory, while carry-over was negligible. Determinations were performed on 170 plasma samples from patients on long-term oral anticoagulant therapy, using the automated amidolytic method; comparison of the prothrombin levels with results obtained by the prothrombin time and Thrombotest methods provided highly significant correlations.
已对一种通过发色底物法测定凝血酶原的市售检测方法在自动临床分析仪上的性能进行了评估。该方法快速简便;准确性、精密度和灵敏度令人满意,而携带污染可忽略不计。使用自动酰胺水解法对170例接受长期口服抗凝治疗患者的血浆样本进行了检测;将凝血酶原水平与通过凝血酶原时间和血栓试验方法获得的结果进行比较,相关性非常显著。