Activation of the fibrinolytic system in patients with fulminant liver failure
Abnormalities of blood coagulation and fibrinolysis are a major part of fulminant liver failure. In this study, the key components of the fibrinolytic system were determined in 42 patients with this condition. Admission levels of plasma plasminogen activity were low (9.1% of normal), as to a lesser...
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Veröffentlicht in: | Hepatology (Baltimore, Md.) Md.), 1993-12, Vol.18 (6), p.1350-1356 |
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Zusammenfassung: | Abnormalities of blood coagulation and fibrinolysis are a major part of fulminant liver failure. In this study, the key components of the fibrinolytic system were determined in 42 patients with this condition. Admission levels of plasma plasminogen activity were low (9.1% of normal), as to a lesser extent were the activities of its inhibitors α2‐antiplasmin (20.5% of normal) and C1 inhibitor (64% of normal). Tissue plasminogen activator activity was found at normal levels, whereas the level of its fast inhibitor, plasminogen activator inhibitor‐1, was greatly increased compared with that of controls (24.3 U/ml and 7.4 U/ml, respectively), indicating a shift toward inhibition of fibrinolysis in these patients. Thrombin‐antithrombin complex levels in plasma were significantly increased in fulminant liver failure compared with those in controls (33.5 μg/L vs. 2.5 μg/L, p < 0.001), indicating activation of coagulation in these patients. High plasma levels of D‐dimer, a fragment of cross‐linked fibrin, were also found (1,510 μg/L vs. 33 μg/L in controls, p < 0.001); this finding correlated with the increased level of thrombin‐antithrombin complex (r = 0.61, p < 0.001), consistent with activation of fibrinolysis resulting from intravascular coagulation. In conclusion, there are gross abnormalities of the fibrinolytic system in fulminant liver failure, but because inhibitory activity appears to be present in adequate quantities, this limits the incidence of bleeding due to fibrinolysis. (HEPATOLOGY 1993;18:1350–1356.) |
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ISSN: | 0270-9139 1527-3350 |
DOI: | 10.1002/hep.1840180611 |