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55 Cards in this Set
- Front
- Back
Anemia lowers the oxygen-carrying capacity of the blood, causing 5 signs of hypoxemia;
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1. Increased cardiac output
2. increased respiratory rate 3. Shunting of blood to vitals--pale skin 4. Decreased Hb O2 affinity which releases more O2 to tissues 5. Increased erythropoietin |
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Clinical signs of anemia:
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Tachycardia
Shortness of breath Systolic flow murmer Fatigability Faintness Angina in elderly Dyspnea on exertion |
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Describe "Hematocrit" or HCT
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Percentage of whole blood occupied by RBCs. Numerically 3x Hb.
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Who has more red cells, males or females, and what hormone is this related to?
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Males, testosterone
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What are the primary RBC measurements?
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RBC count, Hematocrit (HCT), and Hemoglobin concentration (Hb).
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Name the classical indices (2 clinically useful ratios)
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Mean corpuscular volume=average size
Mean corpuscular Hgb concentration=Hb concentration per RBC. |
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What is the equation for MCV?
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Hct/RBC x 10, refers to average size. Normal=87 FL
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What is the equation for MCHC?
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Hgb/Hct x 100, refers to paleness of cell. Normal=34 GM/DL
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What does RDW refer to?
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Red cell distribution width, or the variation of size (anisocytosis) and shape (poikilocytosis), or variation in volume.
<15% is normal. |
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Microcytosis (low MCV) with high RDW diagnoses what disease?
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Iron deficiency
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Microcytosis (low MCV) with normal RDW diagnoses what disease?
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Thalassemia
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A red cell that has lost its nucleous is referred to as what?
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Reticulocyte
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Describe a reticulocyte under Wright-Giemsa stain and reticulocyte stain.
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Wright-Giemsa--bluish
Reticulocyte stain--precipitates RNA, blue with darker clusters. |
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How long is the reticulocyte in the marrow before it enters the bloodstream?
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Two days
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How long is the reticulocyte in the blood before it loses the stainable RNA and becomes mature?
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Twenty-four hours
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Hypoxia of what organ increases EP synthesis?
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Kidney
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Chronic renal failure affects EP how?
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Decreases it, leading to anemia. Can be treated with synthetic EP.
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How long to RBCs live, and what happens to them?
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120 days, and they are phagocytized by macrophages in marrow and spleen at rate of 1% per day.
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The equation for the absolute reticulocyte count:
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raw reticulocyte ratio times the red cell count in x10^3/uL
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When diagnosing anemia, the reticulocyte count determines between what two categories of disease?
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Failure of production (low count)
Failure of Survival (high count) |
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Mean corpuscular volume is useful for diagnosing what type of failure?
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Marrow failure
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Specific red cell shapes are useful for diagnosing what type of failure?
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Failure of RBC survival
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Name the four mechanisms for anemia.
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Blood loss from bleeding
Failure of red blood survival or hemolysis Decreased production: lack of precursors Cecreased production: ineffective erythropoiesis in spite of adequate marrow precursors. |
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Describe reticulocyte count in the first 48 hours, and then 5 days after hemorrhage.
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Normal for the first two days, rises, and peaks at days 5-7.
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Describe the hemoglobin/hematocrit levels during the first 12 hours after hemorrhage.
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Normal unless fluids are given.
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Reticulocytosis occurs when the body increases red cell production how many fold?
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4-fold increase.
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Extrinsic damage to normal red cells occurs through which three major mechanisms?
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Physical destruction
Hypersplenism Immune hemolytic anemia--antibodies |
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What are mechanisms of physical extrinsic damage to normal RBCs?
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Burns, chemicals, distilled water.
Infections Damaged/artificial heart valves DIC |
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Describe what physical damage hypersplenism does to RBCs?
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Cirrhosis, lymphoma, and leukemia trap and destroy RBCs in enlarged spleen--can lead to tear-drop shaped cells.
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Three mechanisms of Immune hemolytic anemia's extrinsic damage to RBCs?
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Autoimmune disease
Blood transfusion--allo-abs in plasma of recipient attack donor red cells Pregnancy--maternal Abs attack red cells in fetus. |
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Coombs Reagent is what?
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Rabbit Ab against human immunoglobulins. Any red cell with human Abs will be agglutinated by adding Coombs reagent.
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Describe Direct Coombs test (DCT)
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Detects human anti-red cell antibodies on patient's rbcs.
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Describe Indirect Coombs test (ICT)
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Detects human anti-red cell antibodies in patients plasma/serum.
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Name two inherited membrane defects of RBCs.
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Spherocytosis
Ovalocytosis |
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Name an acquired membrane defect of RBCs
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Paroxysmal nocturnal hemoglobinuria (PNH). Increases complement-mediated lysis of blood cells.
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What test is important for the diagnosis of defective hemoglobin?
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Hemoglobin electrophoresis
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In what two diseases will you find defective hemoglobin?
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Thalassemia and Hemoglobinopathy.
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Describe the effects of the mutation causing Thalassemia.
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Descreased synthesis of hemoglobin chain, either alpha or beta chains. Will result in the excess of the other, which precipitates out and destroys RBCs by phagocytosis.
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Describe the effects of the mutation causing Hemoglobinopathy.
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Change to one or more of the amino acids of a hemoglobin chain. Results in decreased solubility, crystalized Hb alters RBC shape and membrane causing vascular occlusion and phagocytic destruction of red cell.
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Defective RBC enzymes result in what reaction? What disease does this occur in?
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Leads ot degredation of hemoglobin and forms precipitates which cause phagocytosis.
Seen in G-6-PD deficiency (H2O2 "burns" hemoglobin" |
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Decreased production due to ineffective erythropoiesis causes RBC destruction where?
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In the marrow.
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Ineffective erythropoiesis: iron deficiency looks like what?
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Defective red cells from lack of iron, causes microcytosis.
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Ineffective erythropoiesis: anemia of chronic disease looks like what?
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Chronic inflammation causes macrophages to hoard iron and keep it from erythroblasts. Looks like normocytic anemia but can be severe enough to cause microcytosis.
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Megaloblastic anemia due to ineffective erythropoiesis looks like what?
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Defective red cells, neutrophils, and megakaryocytes from lack of B12, Folate. Causes deficiency of thymidine and inhibits nuclear replication. Looks like macrocytosis (skips divisions)
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95% of megaloblastic anemias are caused by what two deficiencies?
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Vitamin B12 or folate deficiencies.
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A peripheral smear of blood in megaloblastic anemia has the following characteristics;
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Hypersegmented neutrophilic granulocytes
Macrocytes Thrombocytopenia Neuropenia |
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Bone marrow in megaloblastic anemias has the following characteristics;
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Hypercellular
Looks like puffed rice--parachromatin Nuclear/cytoplasmic ansynchrony--nucleus is primitive but cytoplasm matures |
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Four causes of macrocytosis other than B12 and folate deficiences;
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Myxedema
Liver disease Reticulocytosis of any cause Aplastic anemia |
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What is the primary cause of B12 deficiency in the Western world?
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malabosrption
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How is B12 obtained by humans?
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Ingestion of animal products
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How long do B12 stores last in the human body?
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3-4 years
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What is the typical body store for B12 in humans?
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2 mg
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B12 cannot be absorbed in the intestin unless it is linked to what? Where does this come from?
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Intrinsic factor, obtained from parietal cells in the stomach.
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Where does the B12--Intrinsic factor complex attach and absorb?
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Receptors in the ileum
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What two things are required for the attaching of the B12--IF complex to the ileum?
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Ca++ and a neutral pH
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