Podcast
Questions and Answers
What is the primary function of hemostasis?
What is the primary function of hemostasis?
Which of the following is the most potent vasoconstrictor substance released in response to vascular injury?
Which of the following is the most potent vasoconstrictor substance released in response to vascular injury?
What is the role of thrombomodulin in the coagulation cascade?
What is the role of thrombomodulin in the coagulation cascade?
Which protein is responsible for cleaving plasminogen to initiate fibrinolysis?
Which protein is responsible for cleaving plasminogen to initiate fibrinolysis?
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What does activated protein C (APC) form a complex with to cleave factors Va and VIIIa?
What does activated protein C (APC) form a complex with to cleave factors Va and VIIIa?
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Which substance is selective for fibrin-bound plasminogen?
Which substance is selective for fibrin-bound plasminogen?
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Which protein neutralizes all procoagulant serine proteases and inhibits the tissue factor VIIa complex?
Which protein neutralizes all procoagulant serine proteases and inhibits the tissue factor VIIa complex?
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What is the primary function of vascular constriction following an injury to a blood vessel?
What is the primary function of vascular constriction following an injury to a blood vessel?
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Which substance forms a complex with thrombin, activates protein C, and inhibits factor V and VIII in the feedback inhibition on the coagulation cascade?
Which substance forms a complex with thrombin, activates protein C, and inhibits factor V and VIII in the feedback inhibition on the coagulation cascade?
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What is the primary function of α2-antiplasmin in fibrinolysis?
What is the primary function of α2-antiplasmin in fibrinolysis?
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Which factor deficiency results in hemophilia A and von Willebrand’s disease?
Which factor deficiency results in hemophilia A and von Willebrand’s disease?
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What is the approximate half-life of factor II, and how much of the normal level is needed for hemostasis?
What is the approximate half-life of factor II, and how much of the normal level is needed for hemostasis?
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What is the treatment for factor VII deficiency in case of post-operative bleeding?
What is the treatment for factor VII deficiency in case of post-operative bleeding?
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Which factor is responsible for removing lysine residues from fibrin that are essential for binding plasminogen?
Which factor is responsible for removing lysine residues from fibrin that are essential for binding plasminogen?
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What is the treatment for deficiencies of prothrombin or factor X?
What is the treatment for deficiencies of prothrombin or factor X?
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What is the replacement therapy for factor XIII deficiency?
What is the replacement therapy for factor XIII deficiency?
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Which factor deficiency results in hemophilia C?
Which factor deficiency results in hemophilia C?
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What is the role of factor XIII in maintaining adequate hemostasis?
What is the role of factor XIII in maintaining adequate hemostasis?
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What is the effect of having less than one percent normal activity of factors II or prothrombin, V, and X?
What is the effect of having less than one percent normal activity of factors II or prothrombin, V, and X?
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What is the characteristic feature of heparin-induced thrombocytopenia or HIT?
What is the characteristic feature of heparin-induced thrombocytopenia or HIT?
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What is the main pathophysiological mechanism underlying primary immune thrombocytopenia (idiopathic thrombocytopenic purpura - ITP) in adults?
What is the main pathophysiological mechanism underlying primary immune thrombocytopenia (idiopathic thrombocytopenic purpura - ITP) in adults?
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What is the diagnosis method for heparin-induced thrombocytopenia (HIT)?
What is the diagnosis method for heparin-induced thrombocytopenia (HIT)?
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Which disorder is associated with infection by Escherichia coli O157:H7?
Which disorder is associated with infection by Escherichia coli O157:H7?
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What is the primary treatment for hemolytic uremic syndrome (HUS) associated with E. coli infection?
What is the primary treatment for hemolytic uremic syndrome (HUS) associated with E. coli infection?
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What is the recommended treatment for acquired hypofibrinogenemia if the patient is experiencing severe purpura fulminans?
What is the recommended treatment for acquired hypofibrinogenemia if the patient is experiencing severe purpura fulminans?
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What is the recommended initial treatment for acquired hypofibrinogenemia if there is active bleeding?
What is the recommended initial treatment for acquired hypofibrinogenemia if there is active bleeding?
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What is the classic triad of symptoms seen in thrombotic thrombocytopenic purpura or TTP?
What is the classic triad of symptoms seen in thrombotic thrombocytopenic purpura or TTP?
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What is the characteristic feature of idiopathic thrombocytopenic purpura (ITP) in children?
What is the characteristic feature of idiopathic thrombocytopenic purpura (ITP) in children?
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What is the most common underlying condition required for the diagnosis of acquired hypofibrinogenemia?
What is the most common underlying condition required for the diagnosis of acquired hypofibrinogenemia?
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Which of the following can act as potent thromboplastins in acquired hypofibrinogenemia?
Which of the following can act as potent thromboplastins in acquired hypofibrinogenemia?
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What is the effect of ε-aminocaproic acid and tranexamic acid on primary fibrinolysis?
What is the effect of ε-aminocaproic acid and tranexamic acid on primary fibrinolysis?
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Which etiology is associated with acquired hypofibrinogenemia and involves the release of urokinase during surgical manipulation or extracorporeal bypass?
Which etiology is associated with acquired hypofibrinogenemia and involves the release of urokinase during surgical manipulation or extracorporeal bypass?
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In acquired hypofibrinogenemia, which diagnostic parameter is expected to be elevated?
In acquired hypofibrinogenemia, which diagnostic parameter is expected to be elevated?
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Which of the following is a potential cause of acquired hypofibrinogenemia that involves the presence of large aneurysms?
Which of the following is a potential cause of acquired hypofibrinogenemia that involves the presence of large aneurysms?
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What is the mainstay therapy for reducing hypersplenism in patients with coagulopathy of liver disease?
What is the mainstay therapy for reducing hypersplenism in patients with coagulopathy of liver disease?
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Which condition is characterized by shock and tissue injury as key initiators, leading to systemic activation of anticoagulant and fibrinolytic pathways?
Which condition is characterized by shock and tissue injury as key initiators, leading to systemic activation of anticoagulant and fibrinolytic pathways?
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What is the current term used for coagulopathy associated with trauma?
What is the current term used for coagulopathy associated with trauma?
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Which diagnostic test is frequently performed to provide a better assessment of bleeding risks compared to standard tests of hemostasis in patients with liver disease?
Which diagnostic test is frequently performed to provide a better assessment of bleeding risks compared to standard tests of hemostasis in patients with liver disease?
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What is the treatment that forms a complex with thrombin, activates protein C, and inhibits factor V and VIII in the feedback inhibition on the coagulation cascade?
What is the treatment that forms a complex with thrombin, activates protein C, and inhibits factor V and VIII in the feedback inhibition on the coagulation cascade?
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What are the most common coagulation abnormalities associated with liver dysfunction?
What are the most common coagulation abnormalities associated with liver dysfunction?
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What is the management approach for polycythemia to reduce red blood cells, spontaneous thrombosis, and spontaneous hemorrhage?
What is the management approach for polycythemia to reduce red blood cells, spontaneous thrombosis, and spontaneous hemorrhage?
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What is the primary method for reducing hypersplenism in patients with coagulopathy of liver disease?
What is the primary method for reducing hypersplenism in patients with coagulopathy of liver disease?
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What is the recommended treatment for reducing bleeding risks compared to standard tests of hemostasis in patients with liver disease?
What is the recommended treatment for reducing bleeding risks compared to standard tests of hemostasis in patients with liver disease?
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Which therapy is used as the mainstay therapy for polycythemia?
Which therapy is used as the mainstay therapy for polycythemia?
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What is the hallmark feature of antiphospholipid syndrome (APLS)?
What is the hallmark feature of antiphospholipid syndrome (APLS)?
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Which newer anticoagulant has no method for detecting the degree of anticoagulation and no reversal agent?
Which newer anticoagulant has no method for detecting the degree of anticoagulation and no reversal agent?
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In which scenario may surgical treatment be undertaken without full reversal of the anticoagulant?
In which scenario may surgical treatment be undertaken without full reversal of the anticoagulant?
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What is the recommended reversal agent for heparin?
What is the recommended reversal agent for heparin?
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Which condition requires holding heparin infusion for four to six hours before a procedure and restarting it within 12 to 24 hours after the procedure?
Which condition requires holding heparin infusion for four to six hours before a procedure and restarting it within 12 to 24 hours after the procedure?
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What is the primary method for reducing hypersplenism in patients with coagulopathy of liver disease?
What is the primary method for reducing hypersplenism in patients with coagulopathy of liver disease?
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Which substance should be discontinued several days before an operation as part of the reversal strategy for coumarin-derivative anticoagulants?
Which substance should be discontinued several days before an operation as part of the reversal strategy for coumarin-derivative anticoagulants?
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What is the effect of ε-aminocaproic acid and tranexamic acid on primary fibrinolysis?
What is the effect of ε-aminocaproic acid and tranexamic acid on primary fibrinolysis?
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Which factor deficiency results in hemophilia A and von Willebrand’s disease?
Which factor deficiency results in hemophilia A and von Willebrand’s disease?
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What is the characteristic feature of idiopathic thrombocytopenic purpura (ITP) in children?
What is the characteristic feature of idiopathic thrombocytopenic purpura (ITP) in children?
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What is the shelf life of platelet concentrates?
What is the shelf life of platelet concentrates?
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What is the recommended hemoglobin level for autologous transfusion during elective procedures?
What is the recommended hemoglobin level for autologous transfusion during elective procedures?
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What is the therapeutic level of platelets per microliter?
What is the therapeutic level of platelets per microliter?
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What is the product of choice to prevent febrile non-hemolytic transfusion reactions and cytomegalovirus transmission?
What is the product of choice to prevent febrile non-hemolytic transfusion reactions and cytomegalovirus transmission?
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What is the effect of leukocyte-reduced red blood cells?
What is the effect of leukocyte-reduced red blood cells?
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What is the primary function of tranexamic acid?
What is the primary function of tranexamic acid?
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In which surgical settings is tranexamic acid used to decrease bleeding and the need for blood transfusions?
In which surgical settings is tranexamic acid used to decrease bleeding and the need for blood transfusions?
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When is the greatest benefit achieved when administering tranexamic acid after trauma?
When is the greatest benefit achieved when administering tranexamic acid after trauma?
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What is the reduced risk of death due to bleeding associated with tranexamic acid?
What is the reduced risk of death due to bleeding associated with tranexamic acid?
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What are the adverse events associated with prolonged use of tranexamic acid?
What are the adverse events associated with prolonged use of tranexamic acid?
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What is the primary focus of the damage control resuscitation (DCR) strategy?
What is the primary focus of the damage control resuscitation (DCR) strategy?
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What does the term 'permissive hypotension' refer to in the context of resuscitation?
What does the term 'permissive hypotension' refer to in the context of resuscitation?
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What is the recommended volume replacement for symptomatic patients who have lost up to 20 percent of their total blood volume?
What is the recommended volume replacement for symptomatic patients who have lost up to 20 percent of their total blood volume?
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What is the primary aim of administering four to six units of red blood cells within four to six hours of admission under the damage control resuscitation (DCR) strategy?
What is the primary aim of administering four to six units of red blood cells within four to six hours of admission under the damage control resuscitation (DCR) strategy?
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Which factors in the coagulation cascade are measured by activated partial thromboplastin clotting time?
Which factors in the coagulation cascade are measured by activated partial thromboplastin clotting time?
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What is the main purpose of releasing and administering predefined blood products in ratios similar to those of whole blood, as part of the damage control resuscitation (DCR) strategy?
What is the main purpose of releasing and administering predefined blood products in ratios similar to those of whole blood, as part of the damage control resuscitation (DCR) strategy?
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What is the therapeutic target range for the activated partial thromboplastin clotting time?
What is the therapeutic target range for the activated partial thromboplastin clotting time?
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What is the primary aim of conducting the Ivy bleeding time test?
What is the primary aim of conducting the Ivy bleeding time test?
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What is the approximate upper limit of normal bleeding time with the Ivy test?
What is the approximate upper limit of normal bleeding time with the Ivy test?
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Which type of agents may significantly impair hemostatic function?
Which type of agents may significantly impair hemostatic function?
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Apart from known medications, what other factors should be considered if abnormalities in coagulation studies are observed?
Apart from known medications, what other factors should be considered if abnormalities in coagulation studies are observed?
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Which type of heparins may mildly elevate the activated partial thromboplastin clotting time?
Which type of heparins may mildly elevate the activated partial thromboplastin clotting time?
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What is the recommended platelet count to prevent spontaneous hemorrhage?
What is the recommended platelet count to prevent spontaneous hemorrhage?
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In which surgical procedures are platelet transfusions still recommended despite a lack of evidence supporting their use?
In which surgical procedures are platelet transfusions still recommended despite a lack of evidence supporting their use?
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What does the prothrombin time measure the function of?
What does the prothrombin time measure the function of?
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At what platelet count are platelet transfusions still recommended in ophthalmologic and neurosurgical procedures?
At what platelet count are platelet transfusions still recommended in ophthalmologic and neurosurgical procedures?
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At what platelet count is a risk of thrombotic complications present?
At what platelet count is a risk of thrombotic complications present?
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What laboratory test is recommended as the method of choice for reporting prothrombin time values?
What laboratory test is recommended as the method of choice for reporting prothrombin time values?
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What is the primary aim of administering corticosteroids if bleeding follows transfusion by five or six days?
What is the primary aim of administering corticosteroids if bleeding follows transfusion by five or six days?
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What is the normal range for platelet count per microliter?
What is the normal range for platelet count per microliter?
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In the context of excessive intraoperative or post-operative bleeding, what can cause consumptive coagulopathy?
In the context of excessive intraoperative or post-operative bleeding, what can cause consumptive coagulopathy?
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What is an uncommon cause of thrombocytopenia and associated bleeding after transfusion?
What is an uncommon cause of thrombocytopenia and associated bleeding after transfusion?
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In the context of massive transfusion, what can cause hypothermia and dilutional coagulopathy?
In the context of massive transfusion, what can cause hypothermia and dilutional coagulopathy?
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Study Notes
Coagulopathy Management
- In patients with active bleeding, initiate fresh frozen plasma, cryoprecipitate, and fibrinogen concentrates, as well as platelet concentrates.
Fibrinolysis and Antifibrinolytic Agents
- Urokinase is released during surgical manipulation or extracorporeal bypass and can be treated with antifibrinolytic agents, such as ε-aminocaproic acid and tranexamic acid.
Myeloproliferative Diseases
- Treatment for myeloproliferative diseases includes low-dose aspirin, thrombosis phlebotomy, and hydroxyurea.
Coagulation Factors and Liver Disease
- Vitamin K-dependent factors include II (prothrombin), VII, IX, and X.
- Fibrinogen, Factor V, Factor VIII, and Factors XI, XII, and XIII are also involved in coagulation.
- Antithrombin III, plasminogen, protein C, and protein S are relevant to coagulation regulation.
- Liver disease is associated with increased bleeding risk, thrombotic risk, thrombocytopenia, and impaired humoral coagulation function.
- Prothrombin time and international normalized ratio (INR) are commonly prolonged in liver dysfunction.
Diagnostics and Management
- Thrombin Activation and TAFI are diagnostic markers.
- Management of coagulopathy involves treating underlying liver disease and addressing bleeding and thrombotic risks.
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Description
Test your knowledge of the biological process of hemostasis, which functions to limit blood loss from an injured vessel by orchestrating vascular constriction, platelet plug formation, fibrin formation, and fibrinolysis. This quiz covers the physiological events, such as vascular constriction and feedback inhibition.