血栓病:易致静脉血栓栓塞的疾病

MD, FRCP(C), FACP, FCCP Graham F. Pineo (Professor of Medicine and Oncology, Director, Thrombosis Research Unit) , MB BS, MSc, FRCP(C), FACP, FCCP Russell D. Hull (Professor of Medicine, and Director, Thrombosis Research Unit)
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引用次数: 12

摘要

静脉血栓栓塞仍然是临床医生面临的挑战。多年来,已经确定了一些易致静脉血栓栓塞的危险因素,并且在制定预防和治疗这些疾病的建议时考虑了这些危险因素。近年来,我们对先天性或获得性缺陷的理解取得了重大进展,这些缺陷易导致血栓形成,从而导致所谓的获得性或遗传性血栓形成。获得性血栓病的列表现在包括抗凝血酶、蛋白C、蛋白S、活化蛋白C抵抗、凝血酶原20210A突变体、同型半胱氨酸血症和一些罕见的缺陷,这些缺陷要么增强凝血,要么干扰纤维蛋白溶解。尽管取得了这些进展,但仍有许多患有血栓病的家庭,他们没有任何已知的缺陷可以证明。未来的挑战是发现其中一些未知的因素,并确定预防和治疗血栓性疾病易感个体静脉血栓栓塞的最合适方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
1 Thrombophilia: disorders predisposing to venous thromboembolism

Venous thromboembolism continues to present a challenge to clinicians. Over the years, a number of risk factors which predispose to venous thromboembolism have been identified, and these risk factors are taken into account in the formulation of recommendations for the prevention and treatment of these disorders. In more recent years, there have been major advances in our understanding of congenital or acquired defects that predispose to thrombosis leading to these so-called acquired or inherited forms of thrombophilia. The list of acquired forms of thrombophilia now includes anti-thrombin, protein C, protein S, activated protein C resistance, the prothrombin 20210A mutant, homocysteinemia and a number of rare defects which either enhance coagulation or interfere with fibrinolysis. In spite of these advances, there are numerous families with thrombophilia in whom none of the known defects can be demonstrated. The challenge for the future is to discover some of these as yet unknown factors and to determine the most appropriate methods for the prevention and treatment of venous thromboembolism in susceptible individuals with thrombophilia.

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