Advances in our understanding of the biochemistry of the haemostatic mechan
ism have led to the development of sensitive methods for measuring peptides
, enzyme-inhibitor complexes, and enzymes that are liberated with the activ
ation of the coagulation system in vivo. Studies employing these markers ha
ve provided important mechanistic information regarding haemostatic mechani
sm function both under normal conditions and in response to pathogenic stim
uli. While assays for particular components can denote the presence of a 'b
iochemical' hypercoagulable state prior to the appearance of overt thrombot
ic phenomena, most of these markers thus far have not been shown to be usef
ul in managing individual patients. Properly designed prospective studies w
ill be required to determine whether these assay techniques will aid in the
identification of patients predisposed to thrombotic events or the monitor
ing of antithrombotic therapy.