Abstract:Purpose of review
Although recorded evidence of phenotyping bleeding disorders extends back two millennia, standardization of phenotyping has only begun in the past half century. This was spurred by the need for greater precision in diagnosing disorders in order to select proper laboratory tests and treatment, and the realization that the bleeding history provides prognostic information about the future risk of bleeding with surgery or invasive procedures.
Recent findings
New bleeding assessment tools (BATs)… Show more
“…The maximum plasma аXа activity was noted in the 5th minute after the administration of SC BOS-122 and heparin into the blood, which coincides with the literature on the intravenous administration of the direct anticoagulant heparin (James, Coller, 2012). The complete disappearance of the aXa activity in the rabbit plasma was observed with the introduction of only heparin at doses of 0.75 and 1 µg/kg after 170 and 110 minutes, which is consistent with the data on the plasma coagulation time in the APTT and ReаClot-Heparin tests.…”
Background: Experimental studies and analyses of new compounds with different mechanisms of action on systemic haemostasis are relevant for the identification and development of potential pharmacological preparations. Objective: The modified sulphated polysaccharides with anticoagulant and antithrombin activity were studied for haemostasis. Methods: Platelet-rich plasma was obtained by centrifugation at 200 g for 10 minutes. The remaining citrate blood was further centrifuged at 1500 g for 10 min to obtain platelet-poor plasma. The antithrombin activity of the compounds was evaluated in vitro by their effect on the recalcification time, thrombin and prothrombin time of rabbit and human blood plasma stabilized with a 3.8 % sodium citrate solution in the ratio 9:1. Results: The results showed that the anticoagulant activity of the studied sulphates increased with an increasing degree of sulphation. Sulphated polysaccharides showed strong anticoagulant activity in vitro. The experimental results showed a significant increase in the coagulation time of blood plasma in tests for prothrombin and thrombin time. Conclusion: These properties of these components are of particular interest, and further detailed studies of the physicochemical characteristics and mechanisms of action of these molecules should be performed, which will eventually allow them to be used as heparin-like drugs.
“…The maximum plasma аXа activity was noted in the 5th minute after the administration of SC BOS-122 and heparin into the blood, which coincides with the literature on the intravenous administration of the direct anticoagulant heparin (James, Coller, 2012). The complete disappearance of the aXa activity in the rabbit plasma was observed with the introduction of only heparin at doses of 0.75 and 1 µg/kg after 170 and 110 minutes, which is consistent with the data on the plasma coagulation time in the APTT and ReаClot-Heparin tests.…”
Background: Experimental studies and analyses of new compounds with different mechanisms of action on systemic haemostasis are relevant for the identification and development of potential pharmacological preparations. Objective: The modified sulphated polysaccharides with anticoagulant and antithrombin activity were studied for haemostasis. Methods: Platelet-rich plasma was obtained by centrifugation at 200 g for 10 minutes. The remaining citrate blood was further centrifuged at 1500 g for 10 min to obtain platelet-poor plasma. The antithrombin activity of the compounds was evaluated in vitro by their effect on the recalcification time, thrombin and prothrombin time of rabbit and human blood plasma stabilized with a 3.8 % sodium citrate solution in the ratio 9:1. Results: The results showed that the anticoagulant activity of the studied sulphates increased with an increasing degree of sulphation. Sulphated polysaccharides showed strong anticoagulant activity in vitro. The experimental results showed a significant increase in the coagulation time of blood plasma in tests for prothrombin and thrombin time. Conclusion: These properties of these components are of particular interest, and further detailed studies of the physicochemical characteristics and mechanisms of action of these molecules should be performed, which will eventually allow them to be used as heparin-like drugs.
“…Bleeding has always been an alarming clinical symptom in all human societies, and physicians have had varying degrees of success in diagnosing and treating bleeding patients . Unlike other clinical manifestations, however, bleeding is likely to become even more common in the future, largely due to the ever‐increasing use of antiplatelet or anticoagulant drugs in frail patients .…”
Bleeding symptoms are frequently reported even in otherwise healthy subjects, and differentiating a normal subject from a patient with a mild bleeding disorder (MBD) can be extremely challenging. The concept of bleeding rate, that is, the number of bleeding episodes occurring within a definite time, could be used as the unifying framework reconciling the bleeding risk observed in congenital and acquired coagulopathies into a single picture. For instance, primary prevention trials have shown that the incidence of non-major bleeding symptoms in normal subjects is around five per 100 person-years, and this figure is in accordance with the number of hemorrhagic symptoms reported by normal controls in observational studies on hemorrhagic disorders. The incidence of non-major bleeding in patients with MBDs (e.g. in patients with type 1 VWD carrying the C1130F mutation) is also strikingly similar with that of patients taking antiplatelet drugs, and the incidence in moderately severe bleeding disorders (e.g. type 2 VWD) parallels that of patients taking vitamin K antagonists. The severity of a bleeding disorder may therefore be explained by a bleeding rate model, which also explains several common clinical observations. Appreciation of the bleeding rate of congenital and acquired conditions and of its environmental/genetic modifiers into a single framework will possibly allow the development of better prediction tools in the coming years and represents a major scientific effort to be pursued.
“…Bleeding has always been an alarming clinical symptom in all human societies, and physicians have had varying degrees of success in diagnosing and treating bleeding patients [ 1 ]. Because bleeding is part of the human experience, one the most challenging tasks for a physician is to discriminate between “normal” and “pathologic” bleeding.…”
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