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The process of making clots when they are needed and removing clots when they are not |
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Made by platelets attracted by the exposure of the underneath epithelial Not stable |
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Secondary Hemostatic Plug |
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Coagulation factors come in and form fibrin which forms a scab A lot more sturdy |
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Clots where there are not supposed to be any |
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Central cavity of a vessel that is lined with endothelial cells and the glycocalyx |
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Thin coating of protein and carbohydrates |
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Arterioles, Venules, and Capillaries Responsible for carrying platelets and coagulation factors to different areas |
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Constrict to limit blood flow in case of injury |
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Tunica Intima Tunica Media Tunica Adventitia |
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Inner layer Lined with endothelial cells |
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The middle layer Provides support |
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The outer layer Provides support |
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The state of the endothelial cells when they have a negative charge that repels platelets |
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Heparin Surfactant, Thrombomodulin, Tissue Thromboplastin |
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Causes vasodilation and inhibits platelet aggregation |
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Initiated upon injury of a vessel The platelets are activated by exposed collagen and they produce and process Von-Willebrand's Factor |
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Carrier of Factor 8 (FVIII) Aids in platelet aggregation |
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Plasminogen Activator Inhibitor |
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Definition
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Megakaryoblast Promegakaryocyte Granular Promegakaryocyte Mature Megakaryocyte Platelets Influenced by Thrombopoietin (TPO) |
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The 4 Zones of a Platelet |
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Definition
Peripheral Zone Structural Zone Organelle Zone Membrane Zone |
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Made up of glycocalyx, a phospholipid bilayer, and integral proteins Responsible for the platelet's negative charge Contains receptors for substances that cause platelet activation |
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Contains granules, mitochrondria, and glycogen-storing sites |
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Has an open canalicular system that connects the outer surface to the inner surface Has a dense tubular system that synthesizes prostaglandin and thromboxin |
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The vessel wall is damaged Platelets attract to the exposed collagen fibers Platelets adhere to the surface with the help of von-willebrand factor, and prostaglandin 1b (Factor 9) The platelets aggregate together using fibrinogen and secrete their granular content |
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The formation of fibrin Involves the stimulation of Zymogens Growth factors stimulate muscle cells and fibroblasts to replace the cells that were damaged |
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Aid in secondary hemostasis 3 Groups: Prothrombin Group, Fibrinogen Group, Contact Group |
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Includes: -Prothrombin (Factor 2) -Factor 7 -Factor 9 -Factor 10 Produced in the liver Dependent on Vitamin K |
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Found in leafy-green vegetables, liver, and fish Structurally resembles prothrombin Blocked by Warfarin (Coumadin) |
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aka Coumadin Lowers the factors in the prothombin group Blocks vitamin K |
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Includes: -Fibrinogen -Factor 8 -Factor 5 -Factor 13 Activated by thrombin during coagulation FV and FVIII are cofactors that aid in activation |
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Includes: -Factor 11 -Factor 12 -Prekallikrin (PK) -High Molecular Weight Kininogen (HMWK or HK) |
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3 Pathways: Intrinsic, Extrinsic, and Common |
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Consists of enzymes and proteins in the plasma Tested for with the PTT Test Starts with FVII -Activated by HMWK to become FVIIa -FVIIa activates FXI which activated FIX Includes FXII, PK, HMWK, FXI, FIX, FVIII, and Von-Willebrand Factor |
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Enzymes, co-factors, activators, and tissue factors found in the plasma Tested for with the Prothrombin Test (PT Test) Caused by Tissue Factor acting on FVII which activates on FIX Includes Tissue Factor and FVII |
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The other two pathways come together to form fibrin FIX activates FX -FX activates prothrombin -Prothombin becomes thrombin -Thrombin activates fibrinogen -Fibrinogen becomes fibrin Includes: FX, FV, Prothrombin, Fibrinogen, FXIII |
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The process of removing a clot Involves different factors that are used to break down a fibrin clot Main component is the activation of Plasminogen and Plasmin |
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Act as activators or inhibitors Control the fibinolytic system to prevent systematic fibrinolysis that results in bleeding Keeps fibrinolysis from going too far |
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Bleeding Time Platelet Aggregation Prothrombin Time (PT) Activated Partial Thrombin Time (aPTT) Thrombin Time Figures out what factors are not functioning correctly before surgery to prevent death from bleeding |
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Not used too much anymore Make a couple slits on the arm, put pressure on the slits to see how long it takes before no blood comes out Tests for platelet function |
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Replacing Bleeding Time More consistent |
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Makes sure people have the right amount of warfarin |
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Activated Partial Thrombin Time (aPTT) |
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Measures the conversion of fibrinogen to fibrin |
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The color of the tube cap that is used for coagulation lab tests |
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Quantitative or Qualitative |
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Term
Quantitative Platelet Disorders |
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Definition
Thrombocytopenia Thrombocytosis |
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Decrease in the platelet count Bleeding problems occur when the platelet count is less than 50 Can be caused by either increased destruction, decreased production (aplastic anemia), chemotherapy, radiation, splenic sequestration, dilutional problems (massive hemorrhage), or multiple mechanisms |
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Immune Causes of Increased Platelet Destruction |
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Definition
Antibodies destroying platelets ITP Drugs Alloimmune Problems |
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Non-Immune Causes of Increased Platelet Destruction |
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Definition
DIC TTP Hemolytic Uremia Mechanism Destruction |
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Definition
Alcoholism Lipoproliferative Disease Cardiopulmonary Bypass |
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Increased platelets Example is Essential Thrombocytopenia Can be caused by 1 of 3 things: Primary Disorders, Seconday Disorders, or Transient Thrombocytosis |
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Primary Disorders That Cause Thrombocytosis |
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Definition
Disorders that cause increased platelet production and maturation Essential Thrombocythemia (ET) Polycythemia Vera (PV) Chronic Myelogenous Leukemia (CML) |
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Secondary Disorders that Cause Thrombocytosis |
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Definition
Reactive causes such as surgery, hemorrhage, and post-splenectomy |
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Definition
Caused by exercise, child birth, and epinephrine |
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Disorders of Platelet Adhesion Disorders of Platelet Aggregation Hematological Disorders Can be caused by drugs or cardiopulmonary bypass surgery |
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Disorders of Platelet Adhesion |
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Definition
Bernard-Soulier Von-Willebrand Disease |
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Disorders of Platelet Aggregation |
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Definition
Blasmin's Thrombocythemia |
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Hematological Platelet Disorders |
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Definition
Myeloproliferative Disorders Acute Leukemias |
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Drugs that can cause qualitative platelet disorders |
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Definition
Aspirin Alcohol Certain antibiotics |
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Cardiopulmonary Bypass Surgery |
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Definition
Causes abnormal surfaces that cause platelet dysfunction |
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Hereditary Disorders of Secondary Hemostasis |
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Definition
Von-Willebrand Disease Hemophilia A Hemophilia B Fibrinogen Deficiency |
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Definition
Deficiency in FVIII Common in Europe |
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Definition
aka Christmas Factor Deficiency in FIX |
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Definition
Deficiency in Factor 1 (FI) |
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Acquired Disorder of Secondary Hemostasis |
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Definition
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Disseminated Intravascular Coagulation (DIC) |
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Definition
Normal hemostasis is altered Allows uncontrolled formation and lysis of fibrin Can be caused by liver disease, primary fibrinogenolysis, or vitamin K deficiency |
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