Abstract
Hypercoagulable states are clinical conditions of patients who are unusually predisposed to venous or arterial thromboembolism. They are also called thrombophilias or prothrombotic disorders. Numerous congenital or acquired risk factors for hypercoagulable states were identified over the last three decades. Patients with inherited thrombotic disorders, including deficiencies of antithrombin, protein C, or protein S, are referred to as having a congenital hypercoagulable state. These deficiencies are uncommon but strong risk factors for thromboembolism, whereas the more recently discovered genetic variants, such as factor V Leiden and prothrombin variant, are common and weak risk factors, causing disease only in the presence of other factors. Patients with an increased risk of developing thrombotic complications because they are of advanced age, are immobilized, are in a pregnancy or puerperium, are undergoing surgery, are having cancer, and/or are using oral contraceptives or hormone replacement therapy are referred to as having an acquired hypercoagulable state. In these patients, the cause of thrombosis is frequently multifactorial and complex. Identification of such conditions may indicate a need for aggressive prophylaxis during high-risk periods, a need for prolonged treatment after an initial episode of thromboembolism, avoidance of oral contraceptives, and investigation of asymptomatic family members when a familial disorder is identified.
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Kojima, T., Saito, H. (2008). Hypercoagulable States. In: Tanaka, K., Davie, E.W., Ikeda, Y., Iwanaga, S., Saito, H., Sueishi, K. (eds) Recent Advances in Thrombosis and Hemostasis 2008. Springer, Tokyo. https://doi.org/10.1007/978-4-431-78847-8_34
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DOI: https://doi.org/10.1007/978-4-431-78847-8_34
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