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Questions and Answers
What form of iron must Fe3+ be converted to for absorption in the small intestine?
What form of iron must Fe3+ be converted to for absorption in the small intestine?
Which protein primarily stores iron in the liver?
Which protein primarily stores iron in the liver?
Which condition causes jaundice due to destruction of red blood cells?
Which condition causes jaundice due to destruction of red blood cells?
What hormone regulates the release of iron from ferritin when needed?
What hormone regulates the release of iron from ferritin when needed?
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What is one common cause of aplastic anemia?
What is one common cause of aplastic anemia?
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What type of anemia results from insufficient iron replacement leading to small and pale erythrocytes?
What type of anemia results from insufficient iron replacement leading to small and pale erythrocytes?
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What blockage causes post-hepatic jaundice?
What blockage causes post-hepatic jaundice?
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What is the characteristic pigmentation of skin and eyes seen in jaundice?
What is the characteristic pigmentation of skin and eyes seen in jaundice?
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At what stage in development is the primary site of blood cell production located in the liver?
At what stage in development is the primary site of blood cell production located in the liver?
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Which bones are primarily responsible for blood cell production by the mid-20s?
Which bones are primarily responsible for blood cell production by the mid-20s?
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What is the first stage of erythrocyte production?
What is the first stage of erythrocyte production?
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How long do erythrocytes typically live before being destroyed?
How long do erythrocytes typically live before being destroyed?
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What role does erythropoietin (EPO) play in erythrocyte production?
What role does erythropoietin (EPO) play in erythrocyte production?
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What is measured by the hematocrit?
What is measured by the hematocrit?
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Which condition is likely to raise the hematocrit level?
Which condition is likely to raise the hematocrit level?
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What is one effect of exercise training on hematocrit?
What is one effect of exercise training on hematocrit?
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What is the primary function of hemoglobin?
What is the primary function of hemoglobin?
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What happens to heme groups as red blood cells are broken down?
What happens to heme groups as red blood cells are broken down?
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What is the outcome of increasing plasma volume in relation to hematocrit?
What is the outcome of increasing plasma volume in relation to hematocrit?
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What color is unconjugated bilirubin?
What color is unconjugated bilirubin?
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Which component of hemoglobin is responsible for oxygen binding?
Which component of hemoglobin is responsible for oxygen binding?
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What happens to conjugated bilirubin after being metabolized by the liver?
What happens to conjugated bilirubin after being metabolized by the liver?
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How is bilirubin ultimately eliminated from the body?
How is bilirubin ultimately eliminated from the body?
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What happens to the iron from the heme group during the breakdown of hemoglobin?
What happens to the iron from the heme group during the breakdown of hemoglobin?
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Which clinical sign may indicate a more severe condition related to internal bleeding?
Which clinical sign may indicate a more severe condition related to internal bleeding?
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What is a common clinical sign of Deep Vein Thrombosis in the affected limb?
What is a common clinical sign of Deep Vein Thrombosis in the affected limb?
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Which factor is NOT considered a risk factor for developing Deep Vein Thrombosis?
Which factor is NOT considered a risk factor for developing Deep Vein Thrombosis?
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What symptom might a patient with Deep Vein Thrombosis report that could indicate migration of a clot?
What symptom might a patient with Deep Vein Thrombosis report that could indicate migration of a clot?
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When managing a patient suspected of having a Deep Vein Thrombosis, what is the correct action?
When managing a patient suspected of having a Deep Vein Thrombosis, what is the correct action?
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What is the role of thrombin in the coagulation cascade?
What is the role of thrombin in the coagulation cascade?
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Which factor is involved in the process of fibrinolysis?
Which factor is involved in the process of fibrinolysis?
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What condition can result from excessive thrombosis or insufficient fibrinolysis?
What condition can result from excessive thrombosis or insufficient fibrinolysis?
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Which of the following is NOT a potential cause of endothelial injury leading to thrombosis?
Which of the following is NOT a potential cause of endothelial injury leading to thrombosis?
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What is the primary function of tissue plasminogen activator (tPA) during fibrinolysis?
What is the primary function of tissue plasminogen activator (tPA) during fibrinolysis?
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Which of the following best describes the relationship between thrombosis and fibrinolysis?
Which of the following best describes the relationship between thrombosis and fibrinolysis?
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Which condition illustrates the consequence of excessive fibrinolysis?
Which condition illustrates the consequence of excessive fibrinolysis?
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Which mechanism can contribute to hypercoagulability?
Which mechanism can contribute to hypercoagulability?
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Which of these is a result of insufficient B12 and folic acid in erythroblast maturation?
Which of these is a result of insufficient B12 and folic acid in erythroblast maturation?
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What characterizes hemolytic anemia?
What characterizes hemolytic anemia?
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Which condition can lead to dilutional anemia?
Which condition can lead to dilutional anemia?
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What is the primary effect of anemia on cardiovascular function?
What is the primary effect of anemia on cardiovascular function?
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What initiates the process of thrombosis?
What initiates the process of thrombosis?
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What is the role of cytokines released by platelets during primary hemostasis?
What is the role of cytokines released by platelets during primary hemostasis?
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How does tissue factor contribute to coagulation during thrombosis?
How does tissue factor contribute to coagulation during thrombosis?
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Which statement is true regarding hemophilia related to coagulation factors?
Which statement is true regarding hemophilia related to coagulation factors?
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Study Notes
Blood Lifecycle
- Blood cell production sites change with age:
- Fetus: Primarily liver
- Infant: All bones
- Adults (mid 20s+): Ribs, vertebrae, sternum, tibia, and humerus. Production depends on bone marrow fat content.
- Erythrocyte (red blood cell) development:
- Pluripotent stem cell (nucleated)
- Proerythroblast
- Erythroblasts (various stages, progressively less basophilic)
- Reticulocyte (first without a nucleus, short-lived, with remnants); its release increases in acute anemia.
- Erythrocyte (mature red blood cell, ~120 days lifespan).
- Erythrocyte fate:
- Live ~120 days
- Metabolically active; enzymes maintain cell membrane and hemoglobin integrity, transport of ions
- Destroyed by macrophages; hemoglobin is broken down into bilirubin, and iron is recycled to bone marrow by transferrin
- Self-destruction in the spleen.
- Erythropoietin (EPO):
- Released by the kidneys (and possibly other tissues) in response to low oxygen levels
- Stimulates erythroblast (red blood cell precursor) production
- Progression through developmental stages is accelerated.
Hematocrit
- Normal range:
- Females: 35-45
- Males: 40-50
- Measures the percentage of red blood cells in the blood. Factors influencing it:
- Red blood cell formation / destruction
- Plasma volume (hydration)
Hemoglobin
- Function: Binds oxygen molecules
- Structure: 4 heme groups (each with an iron ion) and 4 globin molecules.
- Metabolism: Hemoglobin is broken down by macrophages. Globins are recycled, and heme is broken down into biliverdin (green), then bilirubin (yellow) which is either eliminated in feces (as stercobilin, leading to brown feces) or urine (as urobilin, leading to yellow/amber color). Iron is recycled.
Iron Metabolism
- Iron intake: Absorbed in the small intestine as ferrous (Fe2+) iron (from animal products) or ferric (Fe3+) iron (from plant products).
- Metabolism: Ferric iron is converted to ferrous iron before absorption.
- Transport: Bound to transferrin protein in the blood.
- Storage: Stored in ferritin and hemosiderin, with bone marrow as a primary uptake location for hemoglobin production.
- Release: Iron is released during need for hemoglobin production.
Jaundice
- Yellowish discoloration of the skin and sclera due to excess bilirubin. This is caused by several underlying mechanisms.
Anemia
- Various types of anemia exist, including blood loss anemia (hemorrhagic- acute or chronic), aplastic anemia (bone marrow dysfunction), megaloblastic anemia (defective red blood cell maturation due to lack of B12 or folic acid), hemolytic anemia (red blood cell destruction), dilutional anemia, and more.
Blood Clotting
- Thrombosis:
- Endothelial cell injury
- Vasoconstriction
- Primary hemostasis (platelet activation and aggregation)
- Secondary hemostasis (coagulation cascade activation). The formation of a fibrin mesh.
- Fibrinolysis: Breakdown of clots. Tissue Plasminogen Activator (tPA) is crucial in this process.
- Factors influencing blood clots:
- Abnormal blood flow (stasis or turbulence)
- Endothelial injury
Risk Factors for Thrombosis
(Note: Information is organized by risk factor rather than separate categories as requested.)
- Prothrombotic environment (family history, chronic inflammation, infectious disease, or certain medical conditions).
- Long periods of immobilization (prolonged sitting or travel/driving).
- Dehydration. Certain medications or high risk medical states can also contribute.
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Description
Explore the intricate lifecycle of blood cells, including the production sites that change from fetus to adult and the stages of erythrocyte development. Understand the roles of erythropoietin and the fate of mature red blood cells. This quiz delves into hematology and the physiological processes involved in blood cell formation and maintenance.