chapter 10 alterations in hemostasis
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Chapter 10 Alterations in Hemostasis. Hemostasis. Stopping blood flow Normal: Blood usually fluid Seals broken blood vessels Abnormal: Inappropriate clotting Insufficient clotting. Platelets (Thrombocytes). Thrombopoietin Made in liver, kidney, smooth muscle, bone marrow - PowerPoint PPT PresentationTRANSCRIPT
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Chapter 10Alterations in Hemostasis
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Hemostasis
• Stopping blood flow• Normal:
– Blood usually fluid– Seals broken blood vessels
• Abnormal:– Inappropriate clotting– Insufficient clotting
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Platelets (Thrombocytes)• Thrombopoietin
– Made in liver, kidney, smooth muscle, bone marrow
• Megakaryocytes formed in bone marrow– Break apart to form many platelets
• Platelets live 8–9 days in circulation– Many are stored in spleen– Released when needed
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Question
All but which of the following are true about platelets?a. An enzyme called erythropoietin stimulates their
production. b. They are made from megakaryocytes.c. They originate from the bone marrow.d. They are stored in the spleen.
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Answer
a. An enzyme called erythropoietin stimulates their production.
Rationale: Erythropoietin stimulates the production of RBCs (erythrocytes). The word literally means erythrocyte production. Platelet formation is stimulated by thrombopoietin (thrombus/clot production).
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Mediators of Hemostasis• Chemicals produced by platelets • Released at an injury to:
– Start clotting by reacting with blood proteins– Help platelets stick together – Stimulate wound healing– Help platelets stick to vessel wall– Constrict blood vessels
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Coagulation Factors
• Plasma proteins – Most are synthesized by liver– von Willebrand factor made by endothelium– Circulate as inactive procoagulation factors
• Calcium
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Question
What is the effect of von Willebrand disease on the platelets?
a. Increased platelet aggregationb. Decreased platelet aggregationc. Increased platelet formationd. Decreased platelet formation
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Answer
b. Decreased platelet aggregationRationale: Von Willebrand disease is the most common
hereditary bleeding disorder. It is caused by a deficiency or defect in vWF (which carries a clotting factor). The result of less clotting factor is an inability to clot.
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Vessel Spasm
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Cyclooxygenase Enzymes (COX) Produce Mediators of Hemostasis• Celebrex is a drug
that blocks COX-2• People taking
Celebrex develop increased TXA2 levels
• What problems might they have?
COX-1 COX-2
arachidonic acid
thromboxane A2 prostacyclin
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Intrinsic and Extrinsic Pathways
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Fibrinogen Fibrin
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ScenarioA man had a stroke and the doctor gave him tissue
plasminogen activator (TPA).• Why? What is the doctor trying to accomplish?• One of the man’s relatives wondered why they did
not give him heparin or warfarin instead– What is the difference? Why might TPA be
more appropriate?
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Hypercoagulability• Increased platelet number• Platelet aggregation• Endothelial damage• Increased procoagulation factors• Decreased anticoagulation factors
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Question
Tell whether the following statement is true or false.Hypercoagulability states increase the risk of thrombus
formation.
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Answer
TrueRationale: Hyper- as a prefix means “over” or “too much.”
Coagulation/coagulability means “clotting/the ability to clot.” Hypercoagulability means “increased ability to clot or form thrombi.”
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Scenario:A woman with lupus develops breast cancer.• She is given radiation therapy
– She begins to develop nosebleeds and bruising– Her menstrual period is abnormally heavy
Question:Why did this happen?
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Platelet Disorders
• Decreased platelet levels (thrombocytopenia)– Decreased production– Increased destruction– Platelets used up in forming clots
• Impaired platelet function
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Question
Tell whether the following statement is true or false.Platelet disorders are bleeding disorders.
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Answer
TrueRationale: Because the platelet’s job is to clot, platelet
disorders mean that the platelets cannot do that job. An inability to clot results in bleeding/bleeding disorders.