Ginsberg J S, Siragusa S, Douketis J, Johnston M, Moffat K, Donovan D, McGinnis J, Brill-Edwards P, Panju A, Patel A, Weitz J I
Department of Medicine, McMaster University, Hamilton, Canada.
Thromb Haemost. 1996 Apr;75(4):551-4.
In order to determine the clinical utility of an enzyme immunoassay (EIA) for soluble fibrin in patients with suspected pulmonary embolism (PE), 195 unselected patients with suspected PE underwent blood sampling for measurement of plasma levels of soluble fibrin, and objective testing for PE. A soluble fibrin result of < or = 0.75 micrograms/ml showed a sensitivity of 100% for PE and a specificity of 12.8%, whereas a soluble fibrin result of < or = 1.35 micrograms/ml showed a sensitivity of 90.3% and a specificity of 49.4% for PE. The soluble fibrin assay has potential clinical utility in excluding PE.
为了确定酶免疫测定法(EIA)检测疑似肺栓塞(PE)患者可溶性纤维蛋白的临床实用性,195例未经筛选的疑似PE患者接受了血样采集,以测定血浆可溶性纤维蛋白水平,并对PE进行客观检测。可溶性纤维蛋白结果≤0.75微克/毫升时,对PE的敏感性为100%,特异性为12.8%;而可溶性纤维蛋白结果≤1.35微克/毫升时,对PE的敏感性为90.3%,特异性为49.4%。可溶性纤维蛋白检测在排除PE方面具有潜在的临床实用性。