Abstract
For many years, liver disease has been viewed as a bleeding diathesis; this dogma has now come under challenge with the discovery that some patients with liver disease are also at an increased risk of developing thrombosis. The current understanding is that in liver disease, the haemostatic balance remains as in normal individuals but is reset, with equally reduced levels of coagulant and anticoagulant proteins. Thus it is fragile and easily disturbed resulting in either bleeding or thrombosis, depending on the initial stimulus. This, along with the physiological derangements inherent in liver disease, adds many layers of complexity to the investigation and management of bleeding and thrombosis in patients with liver disease. This chapter aims to address these issues, firstly defining liver disease and its aetiologies, the pathophysiological mechanisms underlying the fragile haemostatic balance, interpretation of screening tests of coagulation in the context of liver disease and finally the management of bleeding and thrombosis in liver disease. Future research is discussed including global assays of coagulation, which provide a more accurate assessment of the haemostatic defect and current clinical trials assessing therapeutic options, such as tranexamic acid, in select clinical contexts.
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Ahmad, S., Hunt, B.J. (2016). Coagulopathy of Liver Disease. In: Gonzalez, E., Moore, H., Moore, E. (eds) Trauma Induced Coagulopathy. Springer, Cham. https://doi.org/10.1007/978-3-319-28308-1_29
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