Owen C A
Department of Pathology, Mayo Clinic, Rochester, Minnesota 55905.
Am J Clin Pathol. 1990 Apr;93(4 Suppl 1):S3-8.
Although the fact that blood clotted when it was released from the body was well known to Hippocrates, Plato, Aristotle, Celsus, and Galen, it was not believed to have any physiologic or pathologic significance. Petit, a surgeon, recognized in the 1730s that clotting was hemostatically important in amputations. Finally, the mechanism of clotting began to be studied by Buchanan (1838), who recognized thrombin; Hammarsten (1875), who purified fibrinogen; and Arthus (1890), who discovered the need for calcium. The fact that platelets existed and had a hemostatic function was developed in the 1800s. Not until the late 1940s did the explosion in the discovery of new clotting factors begin; they now number up to Factor XIII, plus many more that have no Roman numeral designation. Discovery of clotting factors led to their assays. The use of whole blood clotting times was improved by measuring the clotting times of plasma. This was followed by the partial thromboplastin time (PTT) and the activated partial thromboplastin time (APTT). The prothrombin time became an important laboratory test. Specific factors were assayed by progressively more specific tests. These included elements of the fibrinolytic and inhibitory systems. Platelets were counted and their functions measured by bleeding times, clot retraction, adhesion, and aggregation. The diagnosis of hemostatic disorders has improved in parallel with the discoveries of new factors and the development of their precise assays.
尽管希波克拉底、柏拉图、亚里士多德、塞尔苏斯和盖伦都清楚地知道血液从体内流出时会凝结,但人们并不认为这具有任何生理或病理意义。外科医生佩蒂在18世纪30年代认识到,截肢手术中凝血在止血方面很重要。最后,布坎南(1838年)开始研究凝血机制,他发现了凝血酶;哈马斯特恩(1875年)纯化了纤维蛋白原;阿尔图(1890年)发现了凝血需要钙。血小板存在并具有止血功能这一事实是在19世纪发现的。直到20世纪40年代末,新凝血因子的发现才开始激增;现在已知的凝血因子多达十三因子,此外还有许多没有罗马数字编号的因子。凝血因子的发现促使了它们的检测方法的出现。通过测量血浆的凝血时间,全血凝血时间的检测方法得到了改进。随后出现了部分凝血活酶时间(PTT)和活化部分凝血活酶时间(APTT)。凝血酶原时间成为一项重要的实验室检测项目。通过越来越特异的检测方法来检测特定的因子。这些检测方法还包括纤维蛋白溶解和抑制系统的成分。通过计数血小板并测量其出血时间、血块回缩、黏附及聚集功能来评估血小板功能。随着新因子的发现及其精确检测方法的发展,止血障碍的诊断水平也得到了提高。