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58 Cards in this Set
- Front
- Back
What are the RBC characteristics? (6)
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1. Biconcave disc
2. Enucleate 3. Deformable 4. Rouleaux Formation 5. High Concentration of carbonic anhydrase 6. Hb content and binding to gases (O2, CO2, NO) |
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what is Haemoblobin when Fe2+ turn to Fe3+?
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Methaemoglobin
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In the bone marrow, where does erythropoiesis occur?
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Erythroblastic islands.
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How does multipotent stem cell mature into erythrocyte?
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1. Multipotent stem cell
2. Blast forming unit erythroid 3. Colony forming unit erythorid 4. Proerythroblast 5. Basophilic erythroblast (early normoblast) 6. Polychromatic erythroblast (intermediate normoblast) 7. (Late) Normoblast 8. Reticulocyte 9. Erythrocyte |
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Where is erythropoietin produced?
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Fetus: Liver
Adults: Peritubular interstitial cells of kidney (Brain astrocyte & neuron, spleen, testis, lung) |
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What stimulates EPO production?
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Kidney O2 sensor detecting tissue hypoxia
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What is porphyrias
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Disorder of haem synthesis due to abnormal accumulation of porphyrin precursors or porphyrins in the bone marrow or liver
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The ability of RBC to change shape depends on (3)
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1. Biconcave shape
2. Viscosity of the cytoplasm 3. Deformability |
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What are the Integral and Peripheral proteins in an RBC and how are they connected?
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Integral: Glycophorin, Band 3 (Anion transporter)
Peripheral: Spectrin, Actin Glycophorin is connected to spectrin via Protein 4.1 Band 3 is connected to spectrin via Ankyrin |
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What are the major and sub-pathway for energy generation in RBC?
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Major: Emden-Meyerhof pathway
Minor: Methaemoglobi-Reductase Pathway Rapaport-Luebering Shunt Hexose Monophosphate Shunt |
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RBC requires energy for? (4)
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1. Maintaining ion gradients
2. Transporting ion across membrane 3. Preserving membrane structures 4. Maintaining haemoglobin in O2 carrying state |
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What is the purpose of Methaemoglobin-Reductase pathway?
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Maintain Hemoglobin in a reduced state
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What is the purpose of Rapaport-Luebering Shunt?
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Produce 2,3 BPG which regulates hemoglobin oxygen binding affinity
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What is the purpose of Hexose Monophosphate Shunt?
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Produce reduced glutathione
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Reducing power in important in RBC for? (3)
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1. Preventing membrane lipid oxidation
2. Detoxifying oxidants 3. Prevention of globin oxidation and denaturation |
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What are the complications of Beta Thalassemia?
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- Osteoprosis
Transfusion related problems: - Endocrine failure (Iron overload) - Transfusion Hemosiderosis (CHF, liver cirrhosis & carcinoma) - Infection & transfusion reaction |
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What are some disease of RBC (3 categories)
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Hemoglobin: Beta-thalassemia, Sickle Cell Anemia
Membrane: Hereditary Spherocytosis, Hereditary Elliptocytosis, Hereditary Pyropoikilocytosis, Hereditary Stomatocytosis Enzyme: G6PD Deficiency, Pyruvate Kinase Deficiency |
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What causes Hereditary Spherocytosis?
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Mutation in "Vertical support components"
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What is Splenic conditioning
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Progressive loss of membrane of RBC during each cycle through the spleen.
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What is the treatment of Hereditary Spherocytosis?
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- Folate supplement
- Spleen protection - Splenectomy |
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What causes Hereditary Spherocytosis?
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Mutation in "Horizontal support components"
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What is Hereditary Pyropoikilocytosis?
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Sensitivity of RBCs to heat
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What causes Hereditary Stomatocytosis?
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Defect in membrane ionic transport proteins in RBC
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What causes South Asian Ovalocytosis?
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Mutation in Band 3 protein in RBC
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How much iron do we lose in a day?
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Men: 1 mg/day
Women 2 mg/day |
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What transport iron into and out of enterocytes?
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In: DMT1 (Ferrous Iron Transporter)
Out: Ferroportin |
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What protein transport iron in blood?
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Transferrin
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What protein is responsible for iron storage in cells?
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Ferritin
Hemosiderin |
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What is the key regulator of iron metabolism?
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Hepcidin
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What is Erythrocyte Protoporphyrin?
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Measure of Zinc Protoporhphyrin, which indicate iron available for hemoglobin production.
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What is protoporphyria?
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A hereditary disease caused by a deficiency of ferrochelatase. Associated with very high FEP values.
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What disease do labs check for blood donors?
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- HIV, HTLV
- Hep B & C - CMV - Syphilis |
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In transfusion, the collected blood is separated into what components?
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- Packed Red Cell
- Platelet - Plasma - Cryoprecipitate |
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Why should blood products be Leukoreduced?
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1. Decreased Febrile reactions
2. Decrease transmission of intracellular infections 3. Decreased HLA alloimmunization |
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What is in Cryoprecipitate?
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- Fibrinogen
- Factor VIII - von Willebrand factor |
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What are the manufactured blood products?
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- Albumin
- IVIG - Factor VIIa, VIII |
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For blood transfusion, what does recipient testing involve?
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1. Type and Screen
2. Crossmatch |
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During transfusion, how does the body respond to carbohydrate and protein?
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Carbohydrate: IgM (Acute Hemolytic Transfusion Reaction)
Protein: IgG (Delayed Hemolytic Transfusion Reaction, Hemolytic Disease of Newborne) |
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Which autoantibodies are considered cold and warm?
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Cold: IgM
Warm: IgG |
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Indications for giving packed RBC
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1. Increase O2 carrying capacity
2. Dilute sickled red cells |
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Indications for giving Platelets
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1. Decreased platelet counts + bleeding/bruising
2. Prophylasix (Pre-op or < 10) 3. Dysfunctional platelets + bleeding/bruising |
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Contraindications for giving Platelets
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Relative:
1. ITP 2. Hypersplenism Absolute: 1. TTP 2. HITT |
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Indications for giving Fresh Frozen Plasma
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1. "Global" Factor Deficiency + bleeding/bruising (Excess Coumadin, Vit K deficiency, DIC, Liver Disease)
2. Prophylaxis (Pre-op) |
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Indications for Cryoprecipitate
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1. Decreased Fibrinogen + bleeding/bruising
2. Dysfunctional Fibrinogen + bleeding/bruising 3. Last resort for Von Willebrand or hemophilia patients |
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What are the 4 types of transfusion reactions?
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1. Immune
2. Infectious 3. Fluid 4. Electroytes/Irons |
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What does immune transfusion reaction consist of?
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- AHTR
- DHTR - Febrile - Allergic - Anaphylactic |
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What does fluid transfusion reaction consist of?
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- Fluid overload
- Hypothermia |
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What does Electrolyte transfusion reaction consist of?
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- Inc K+
- Inc Fe2+ - Dec Ca2+ |
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What is the definition of anemia?
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Reduced hemoglobin concentration relative to "normal"
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What can cause microcytic anemia?
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- Iron Deficiency
- Thalassemia - Anemia of chronic disease - Hemoglobinopathies - Lead Toxicity |
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What can cause punctate basophilia? (4)
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- Thalassaemia
- Siderblastic anaemia - Severe megaloblastic anemia - Lead poisoning |
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What can cause normocytic anemia?
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- Hemolytic Anemia
- Anemia of Chronic Disease - Renal Failure - Combined B12 & Folate - Endocrine abnormalities - Aplastic Anemia - Acute Hemorrhage |
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What can cause macrocytic anemia?
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- B12/Folate Deficiency
- Antimetabolite Chemotherapy - Liver Disease - Reticulocytosis - Hypothyroidism - Myelodysplastic Syndrome |
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What can cause oval macrocytes?
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- MDS
- Megaloblastic |
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What can cause target cells?
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- Thalasemia
- Liver disease - Iron deficiency |
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What can cause Pencil cells?
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Iron deficiency anemia
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What can cause Howell-Jolly body
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Sickle Cell Anemia
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What can cause Rouleaux Formation?
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Multiple myeloma
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