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Why is there no elevated D-dimer in excess fibrinolysis?
D-dimer is a measure of fibrin split products. With excess plasmin you're breaking down both fibrin and fibrinogen, so why wouldn't there be fibrin split products?
D-dimer is a measure of fibrin split products. With excess plasmin you're breaking down both fibrin and fibrinogen, so why wouldn't there be fibrin split products?
