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D - 二聚体、凝血酶 - 抗凝血酶III复合物及凝血酶原片段1 + 2:对临床疑似深静脉血栓形成的诊断价值

D-Dimers, thrombin antithrombin III complexes and prothrombin fragments 1+2: diagnostic value in clinically suspected deep vein thrombosis.

作者信息

Boneu B, Bes G, Pelzer H, Sié P, Boccalon H

机构信息

Laboratoire d'Hémostase, Centre de Transfusion Sanguine, Toulouse, France.

出版信息

Thromb Haemost. 1991 Jan 23;65(1):28-31.

PMID:2024237
Abstract

This study was performed to determine the accuracy of D-Dimer fibrin derivatives, thrombin-antithrombin III (TAT) complexes and prothrombin fragments 1 + 2 (F 1 + 2) determinations for the diagnosis of deep vein thrombosis (DVT). One hundred and sixteen consecutive patients referred to the angiology unit of our hospital for a clinically suspected DVT were investigated. They were submitted to mercury strain gauge plethysmography and to ultrasonic duplex scanning examination; in cases of inconclusive results or of proximal DVT (n = 35), an ascending phlebography was performed. After these investigations were completed, the diagnosis of DVT was confirmed in 34 and excluded in 82. One half of the patients were already under anticoagulant therapy at the time of investigation. The 3 biological markers were assayed using commercially available ELISA techniques and the D-Dimer was also assayed with a fast latex method. The normal distribution of these markers was established in 40 healthy blood donors. The most accurate assay for the diagnosis of DVT was the D-Dimer ELISA which had both a high sensitivity (94%) and a high negative predictive value (95%). The D-Dimer latex, TAT complexes and F 1 + 2 were far less sensitive and provided negative predictive values which ranged between 78 and 85%. In spite of positive and significant correlations between the levels of the 3 markers, their association did not improve their overall accuracy for detecting DVT. Therefore, with the exception of the D-Dimer ELISA, these markers were of little value for the diagnosis of DVT in this specific population.

摘要

本研究旨在确定D - 二聚体纤维蛋白衍生物、凝血酶 - 抗凝血酶III(TAT)复合物和凝血酶原片段1 + 2(F 1 + 2)检测对诊断深静脉血栓形成(DVT)的准确性。对连续116例因临床疑似DVT转诊至我院血管病科的患者进行了调查。他们接受了水银应变计体积描记法和超声双功扫描检查;对于结果不明确或近端DVT患者(n = 35),进行了上行静脉造影。这些检查完成后,34例患者确诊为DVT,82例排除DVT。一半患者在调查时已接受抗凝治疗。使用市售ELISA技术检测3种生物标志物,D - 二聚体还采用快速乳胶法检测。在40名健康献血者中确定了这些标志物的正常分布。诊断DVT最准确的检测方法是D - 二聚体ELISA,其具有高灵敏度(94%)和高阴性预测值(95%)。D - 二聚体乳胶、TAT复合物和F 1 + 2的敏感性远低于前者,阴性预测值在78%至85%之间。尽管3种标志物水平之间存在正相关且具有显著性,但它们的联合使用并未提高检测DVT的总体准确性。因此,除D - 二聚体ELISA外,这些标志物在该特定人群中对DVT的诊断价值不大。

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