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Coagulant and anticoagulant
Coagulants and anticoagulants work in opposing ways to regulate blood coagulation. Coagulants such as vitamin K and plasma fractions help promote coagulation by activating clotting factors. Anticoagulants like heparin and warfarin inhibit coagulation factors or their production. Thrombolytics such as streptokinase and tissue plasminogen activator dissolve clots by activating plasmin. Platelet aggregation inhibitors including aspirin and clopidogrel prevent platelet activation and aggregation, which are key steps in clot formation. These drugs are used to treat and prevent thrombotic conditions.
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Introduction to coagulants and their role in haemostasis, including Vitamin K functions and plasma factors.Discussion on the types of anticoagulants, their mechanisms, uses in vivo and in vitro, and monitoring.
Fibrinolytic agents used to dissolve blood clots and their applications in various medical conditions.
Types of platelet aggregation inhibitors, their mechanisms, and clinical uses in preventing thrombotic events.
Appreciation for the presentation and its content on coagulants, anticoagulants, thrombolytics, and aggregation inhibitors.
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Coagulant and anticoagulant
- 1. Coagulant and anticoagulant S. Parasuraman,M.Pharm., Ph.D., Senior Lecturer, Faculty of Pharmacy, AIMST University Scanning electron micrograph of platelets
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- 3. Coagulant • Haemostasis (arrestof blood loss) and blood coagulation involve complex interactions between the injured vessel wall, platelets and coagulation factors.
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- 5. Coagulants Vitamin K K1(from plants fat-soluble): Phytonadione (Phylloquinone) K3 (synthetic) —Fat-soluble: Menadione, Acetomenaphthone —Water-soluble: Menadione sod. Bisulfite, Menadione, sod. Diphosphate Miscellaneous Fibrinogen (human), Antihaemophilic factor, Desmopressin, Adrenochrome monosemicarbazone, Rutin, Ethamsylate
- 6. Vitamin K • Vit.K is a fat-soluble dietary principle required for the synthesis of clotting factors. • Daily requirement: Vit. K2 produced by colonic bacteria and 3–10 μg/day external source may be sufficient. The total requirement of Vit. K for an adult has been estimated to be 50–100 μg/day.
- 7. Vitamin K Functional formInactiveform Vit. K Vit. K
- 8. Vitamin K Action: Vit Kacts as a cofactor at a late stage in the synthesis by liver of coagulation proteins - prothrombin, factors VII, IX and X. Use: The only use of vit K is in prophylaxis and treatment of bleeding due to deficiency of clotting factors.
- 9. Coagulants Plasma fractions • Deficienciesin plasma coagulation factors can cause bleeding. • Factor VIII deficiency (classic hemophilia or hemophilia A) and factor IX deficiency (Christmas disease, or hemophilia B) account for most of the heritable coagulation defects. Concentrated plasma fractions and recombinant protein preparations are available for the treatment of these deficiencies.
- 10. Coagulants Desmopressin acetate • Desmopressin(DDAVP) stimulates the release of von Willebrand factor (vWF) from the Weibel–Palade bodies of endothelial cells, thereby increasing the levels of vWF (as well as coagulant factor VIII) 3 to 5- fold. • It also used to promote the release of von Willebrand factor in patients with coagulation disorders such as von Willebrand disease, mild hemophilia A and thrombocytopenia.
- 11. Coagulants Cryoprecipitate • Cryoprecipitate isa plasma protein fraction obtainable from whole blood. It is used to treat deficiencies or qualitative abnormalities of fibrinogen. • It may also be used for patients with factor VIII deficiency and von Willebrand disease
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- 13. Anticoagulants Used in vivo Parenteral anticoagulants Indirect thrombininhibitors: Heparin, Low molecular weight heparins, Fondaparinux, Danaparoid Direct thrombin inhibitors: Lepirudin, Bivalirudin, Argatroban Oral anticoagulants Coumarin derivatives: Bishydroxycoumarin (dicumarol), Warfarin sod, Acenocoumarol (Nicoumalone), Ethylbiscoumacetate Indandione derivative: Phenindione Direct factor Xa inhibitors: Rivaroxaban Oral direct thrombin inhibitor: Dabigatran etexilate
- 14. Anticoagulants Used in vitro Heparin 150U to prevent clotting of 100 ml blood. Calcium complexing agents: Sodium citrate 1.65 g for 350 ml of blood (used to keep blood in the fluid state for transfusion) Sodium oxalate 10 mg for 1 ml blood (used in blood taken for investigations) Sodium edetate 2 mg for 1 ml blood (used in blood taken for investigations)
- 15. Blood clotting factors and drugsthat affect them
- 16. Anticoagulant • The anticoagulantdrugs inhibit either the action of the coagulation factors (heparin) or interfere with the synthesis of the coagulation factors (warfarin). • Heparin or Unfractionated heparin (UFH) is a heterogeneous mixture of sulfated mucopolysaccharides with MW 10,000 to 20,000 g/mol. Its biologic activity is dependent upon the endogenous anticoagulant antithrombin.
- 17. Anticoagulant • The shorter-chain,low-molecular-weight (LMW) fractions of heparin (enoxaparin, dalteparin, and tinzaparin) inhibit activated factor X but have less effect on thrombin than the high-molecular-weight (HMW) species. • Monitoring of Heparin Effect: Close monitoring of the activated partial thromboplastin time (aPTT or PTT) is necessary in patients receiving UFH. Levels of UFH may also be determined by protamine titration (therapeutic levels 0.2–0.4 unit/mL) or anti-Xa units (therapeutic levels 0.3–0.7 unit/mL).
- 18. Anticoagulant • Toxicity: Bleeding,loss of hair and reversible alopecia, heparin-Induced thrombocytopenia. • Contraindications: Heparin should be avoided in patients who have recently had surgery of the brain, spinal cord, or eye; and in patients who are undergoing lumbar puncture or regional anesthetic block. • Reversal of Heparin Action: Protamine antagonize the heparin. Intravenous injection of protamine neutralises heparin weight for weight, i.e. 1 mg is needed for every 100 U of heparin.
- 19. Use of anticoagulant •The aim of using anticoagulants is to prevent thrombus extension and embolic complications by reducing the rate of fibrin formation. – Deep vein thrombosis and pulmonary embolism – Myocardial infarction – Unstable angina – Rheumatic heart disease; Atrial fibrillation – Cerebrovascular disease – Vascular surgery, prosthetic heart valves, retinal vessel thrombosis, extracorporeal circulation, haemodialysis – Defibrination syndrome
- 20. Direct factor Xainhibitors • Rivaroxaban: It is an orally active direct inhibitor of activated factor Xa which has become available for prophylaxis and treatment of Deep Vein Thrombosis (DVT). Oral direct thrombin inhibitor • Dabigatran etexilate: It is a prodrug which after oral administration is rapidly hydrolysed to dabigatran, a direct thrombin inhibitor. Dabigatran reversibly blocks the catalytic site of thrombin and produces a rapid anticoagulant action.
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- 22. Thrombolytics Streptokinase, Urokinase, Alteplase(rt-PA), Reteplase Tenecteplase: • These are drugs used to lyse thrombi/clot to recanalize occluded blood vessels (mainly coronary artery). • Streptokinase is a protein synthesized by Streptococci that combines with the proactivator plasminogen. • Urokinase is a human enzyme synthesized by the kidney that directly converts plasminogen to active plasmin.
- 23. Thrombolytics Streptokinase, Urokinase, Alteplase(rt-PA), Reteplase Tenecteplase: • Uses of fibrinolytics: • Administration of fibrinolytic drugs by the i.v. route is indicated in cases of pulmonary embolism with hemodynamic instability, severe deep venous thrombosis such as the superior vena caval syndrome, and ascending thrombophlebitis of the iliofemoral vein with severe lower extremity edema. • These drugs are also given intra-arterially, especially for peripheral vascular disease.
- 24. Platelet aggregation inhibitors Imagesource: Jackson SP. The growing complexity of platelet aggregation. Blood. 2007;109(12):5087-95.
- 25. Platelet aggregation inhibitors Aspirin: •Platelet aggregation inhibitors decrease the formation of a platelet-rich clot or decrease the action of chemical signals that promote platelet aggregation. • The platelet aggregation inhibitors described below inhibit cyclooxygenase-1 (COX-1) or block GP IIb/IIIa or ADP receptors, thereby interfering with the signals that promote platelet aggregation. • Use: Aspirin is used in the prophylactic treatment of transient cerebral ischemia.
- 26. Platelet aggregation inhibitors Ticlopidine,clopidogrel, prasugrel, and ticagrelor: • These drugs inhibit the binding of ADP to its receptors on platelets and, thereby, inhibit the activation of the GP IIb/IIIa receptors required for platelets to bind to fibrinogen and to each other. Ticagrelor binds to the P2Y12 ADP receptor in a reversible manner. • Use: Clopidogrel is approved for prevention of atherosclerotic events in patients with a recent MI or stroke and for prophylaxis of thrombotic events in acute coronary syndromes.
- 27. Platelet aggregation inhibitors Ticlopidine,clopidogrel, prasugrel, and ticagrelor: • Use: Ticlopidine is indicated for the prevention of transient ischemic attacks and strokes in patients with a prior cerebral thrombotic event. It is generally reserved for patients who are intolerant to other therapies. • Prasugrel is approved to decrease thrombotic cardiovascular events in patients with acute coronary syndromes. • Ticagrelor is approved for the prevention of arterial thromboembolism in patients with unstable angina and acute MI.
- 28. Platelet aggregation inhibitors Abciximab,eptifibatide, and tirofiban: • A chimeric monoclonal antibody, abciximab, eptifibatide inhibits the glycoprotein IIb/IIIa receptor complex. • Use: These agents are given intravenously, along with heparin and aspirin, as an adjunct to percutaneous coronary intervention (PCI) for the prevention of cardiac ischemic complications.
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