Hema-

Subdecks (2)

Cards (139)

  • Hematology
    The study of blood cells
  • Athanasius Kircher (1657) described worms in the blood
  • Anton van Leeuwenhoek (1674) gave an account of RBCs
  • Giulio Bizzozero (late 1800s) described platelets as "petites plaques"
  • James Homer Wright (1902) developed Wright stain
  • In the present day, Hematology laboratory is analyzed by automation
  • Functions of blood
    • Transport oxygen from lungs to tissues
    • Clear tissues of carbon dioxide
    • Transport glucose, proteins, and fats
    • Move waste to the liver and kidneys
  • The average human has 5 liters of blood
  • Plasma
    Liquid portion of anticoagulated blood
  • Serum
    Liquid portion of a clotted blood
  • Anti-coagulant
    Not coagulant, unclotted
  • Coagulant
    Clotted, with fibrinogen
  • Three categories of blood cells
    • Red blood cells or erythrocytes
    • White blood cells or leukocytes
    • Platelets or thrombocytes
  • Red blood cells
    • Biconcave, discoid cells
    • Filled with hemoglobin which transports oxygen and carbon dioxide
    • Appear pink to red, 6-8um in diameter with a zone of pallor in the center
  • Anemia
    Loss of oxygen carrying capacity reflected in a reduced RBC count or decreased RBC hemoglobin concentration
  • Polycythemia
    Increased RBC count reflecting increased circulating RBC mass, leading to hyperviscosity
  • RBC counting
    1. Carefully pipette a tiny aliquot of whole blood
    2. Mix with 0.85% normal saline solution with a dilution of 1:200
    3. Transfer to a glass counting chamber called Hemocytometer
  • Osmosis
    The movement of water in a semipermeable membrane from a lower solute concentration to a higher solute concentration
  • Isotonic
    Same osmolality or solute concentration as another solution, RBCs will neither shrink nor swell
  • Hypotonic
    Solute concentration is lesser than the other solution, RBCs will swell and eventually lyse
  • Hypertonic
    Solute concentration is greater than the other solution, RBCs will shrink or crenate
  • The Coulter counter principle is based on direct current electrical impedance
  • White blood cells/Leukocytes
    • A loosely related category of cell types dedicated to protecting their host from infection and injury
    • Counted with the same technique as RBCs but with a typical dilution of 1:20 and a dilute acid solution as the diluent
  • Leukocytosis
    WBC count of >11,500
  • Leukopenia
    WBC count of <4500
  • Types of WBCs
    • Neutrophils
    • Eosinophils
    • Basophils
    • Lymphocytes
    • Monocytes
  • Neutrophilia
    Increase in neutrophils, common cause: Bacterial infection
  • Neutropenia
    Decrease in neutrophils, common cause: certain medications or viral infections
  • Left shift

    Increase in band neutrophils, commonly found in bacterial infection
  • Eosinophilia
    Elevated eosinophil count, signifies a response to allergy or parasitic infection
  • Basophilia
    Rare, often signals a hematologic disease
  • Lymphocytosis
    Associated with viral infections
  • Lymphocytopenia
    Associated with drug therapy or immunodeficiency
  • Monocytosis
    Associated with collagen-vascular disease, or in acute and chronic leukemias
  • Platelets/Thrombocytes
    • True blood cells that maintain blood vessel integrity by initiating vessel wall repairs
    • Come from the cytoplasm of the megakaryocytes
    • Function: Adhere/Adhesion to the site of injury, Aggregate/Aggregation with other platelets to form the platelet plug, Secret/Secretion the contents of their granules
    • Only 6-8um round or oval, and anucleate
  • Thrombocytosis
    Increase in platelet count
  • Thrombocytopenia
    Decrease in platelet count
  • Complete Blood Count
    1. Performed on automated blood cell analyzers to assess adequate blood cells
    2. The MLS is responsible for the integrity of the specimen and ensures: Proper anticoagulant used, Free of clots, Not hemolyzed, Sufficient in volume, Tested within turn-around time
    3. If one result is abnormal, the instrument will display a flag and a blood film examination is performed
    4. If results are normal, a blood film examination is not needed
  • Blood Film Examination
    1. Prepare a wedge-prep blood film on a glass slide, allow it to dry, and fix and stain it using Wright or right-Giemsa stain
    2. Use 40x objective for WBCs, 100x oil immersion objective for platelets
    3. Review, identify, and tabulate 100 (or more) WBCs to determine their percentage distribution aka the WBC differential/Diff count
    4. Examine the morphology of blood cells using 1000x magnification
  • Main function of blood film examination
    Confirm/verify the results of automated analyzers