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Investigation of Haemostasis.
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HHHHaemostasis is the arrest of blood loss from damaged vessels. TTTThe haemostatic mechanisms have two primary functions: To ensure that circulating blood remains fluid while in the vascular bed. And to arrest bleeding at the site of an injured blood vessel.
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TTTTo fulfill that: BBBBlood must be fluid MMMMust coagulate (clot) at appropriate time Rapid Localized Reversible
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The normal haemeostasis depends on a delicate balance and complex interaction between at least five components: PPPPlatelet. BBBBlood vessels. PPPPlasma coagulation proteins. 4444+5. Inhibitors and the fibrinolytic system.
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Vascular haemostasis.
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HHHHumans have evolved an intricate hemostatic system that is designed to maintain blood in a fluid state under physiologic conditions, but that is primed to react to vascular injury in an explosive manner to stem blood loss by sealing the defect in the vessel wall. TTTThe blood cell wall has three layers: intima, media and adventitia. TTTThe intima consists of the endothelium and subendothelial connective tissue and is separated from the media by the elastic lamina interna. EEEEndothelium cells form a continuous monolayer lining all blood vessels.
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T T T The function and the structure of these cells are vary according their location in the vascular tree, but they are all share three important characteristics: TTTThey are "non thrombogenic" that is do not react with plasma or the cellular elements of the blood. TTTThey play an active role in supplying nutrients to the subendothelial structures. AAAAnd act as a barrier to macromolecules and particles matter circulating in the blood stream. TTTThe intact vessel wall has an important role in preventing haemostasis.
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EEEEndothelial cells produce: PPPProstacyclin, which causes vasodilatation and inhibits platelets aggregation. PPPProtein C (PC) activator (Thrombomodulin), which inhibits coagulation. AAAAnd tissue plasminogen activator (TPA) which activates fibrinolysis.
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Endothelial cell function 1: TTTThe luminal surface of the endothelial cell is covered by Glycocalyx coat. IIIIt contains heparin sulphate and other substances which are capable of activating antithrombin III, an important inhibitor of coagulation enzymes. BBBBeneath the glycocalyx, there is a trilaminar membrane containing ADPase, an enzyme which degrades ADP which is a potent platelets agonist. TTTThe endothelial cells can also generate angiotensin II, a local vasoconstrictor.
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Endothelial cell function 2: TTTThrombin generated at the site of the injury is rapidly bound to a specific cofactor of the endothelial cell, Thrombomodulin. When bound this protein, thrombin can activate the protein C system to degrade and inhibit factor Va and VIIIa. TTTThrombin can also stimulate the endothelial cells to produce plasminogen activator. FFFFinally, the endothelial cells produces von Willebrand factor (vWF), essential for platelets adhesion to the subendothelium. vWF is secreted partly into the circulation and partially towards the subendothelial matrix.
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The subendothelium: TTTThe subendothelium is consists of connective tissues composed of collagen, elastic tissues, proteoglycans, fibronectin and vWF. AAAAfter endothelial damage has taken place, components of subendothelium are exposed and platelets adhere to various elements collagen of basement membrane and micofibrils. TTTThe adhesion of platelets is regulated by specific properties of the platelet membranes and biochemical characteristics of the subendothelial structures. OOOOther factors, such as plasma concentration of vWF and the characteristics of the blood flow also effect adhesion.
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Vasoconstriction: VVVVessels with muscular coat contract following injury, thus assisting haemostatic plug formation by reducing the blood flow. VVVVasoconstriction occurs, however, even in the microcirculation in vessels without smooth muscle cells. EEEEndothelial cells can themselves produce vasoconstrictors such as angiotensin II; in addition, activated platelets produce prostaglandins (TXA2) with vasoconstricting properties.
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Investigation of the Disorders of Vascular Haemostasis: TTTThe disorder this part may be due to increase permeability, reduction of vessels strength and failure to contract in injury. AAAAn accurate history and careful clinical examination are almost always the keystone of diagnosis. TTTTests of defective vascular function are difficult to perform and interpret. TTTTests of capillary resistance are of limited value. IIIIn some cases skin biopsy with specific staining or even biochemical analysis of the micro-sample may be helpful. TTTThe bleeding time test is normal and the other tests of haemostasis are also normal.
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Capillary fragility (resistance) test: TTTThis test is used to determine the presence of vascular disorder, a circle 2.5 cm in diameter, the upper edge of which is 4 cm below the crease of the elbow, is drawn on the inner aspect of the forearm, pressure midway between the systolic and diastolic blood pressure is applied using sphygmomanometer above the elbow for 15 minutes, and a count of p p p p p eeee tttt eeee cccc hhhh iiii aaaa eeeewithin the circle is made: 10, normal; 10–20, marginal; more than 20, abnormal.
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