Chapter 23 Flashcards

1
Q

Red blood cell development

A

. Erythroblasts are continuously being formed from the pluripotent stem cells in the bone marrow

  • They move through a series of divisions to develop into mature red blood cells.
  • Normoblast to reticulocyte, the red blood cells accumulates hemoglobin as the nucleus condensed and is lost.
  • The red cell loses its mitochondria and ribosomes.
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2
Q

Function of the red blood # 1

A

. Transportation of oxygen to the tissues
- Hemoglobin binds some carbon dioxide and carried it from the tissues to the lungs
- The hemoglobin molecule is composed of two pairs of structurally different polypeptide chains.
. Each of the four polypeptide chains consist of a globin (protein) portion and heme unit, which surrounds an atom of iron that binds oxygen

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3
Q

Function of red blood # 2

A
  • Each molecule of hemoglobin can carry four molecules of oxygen
    . The production of each type of globin chain is controlled by individual structural genes with five different gene loci
    -Mutations can occur anywhere in these five loci
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4
Q

Erythropoiesis

A

. Red cells are produced in the red bone marrow after birth
. Until 5 years of age, almost all bones produce red cells to meet growth needs; after 5 years, bone marrow activity gradually declines.
. After 20 years, red cell production takes place mainly in the membranous bones of the vertebrae, sternum, ribs and pelvis.
. With this reduction in activity, the red bone marrow is replaced with fatty yellow bone marrow.

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5
Q

Hemoglobin Structure

A
. Globin
-a
-B beta
. Heme
-Iron
-porphyrin 
. Oxygen binding
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6
Q

Red Blood Cell destruction

A

. The red blood cell has a life span of approximately 120 days
- It is broken down in the spleen
- The degradation products (iron and amino acids) are recycled.
. The heme molecule is converted to bilirubin and transported to the liver.
- it is removed and rendered water soluble for elimination in the bile.

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7
Q

Bilirubin

A

. The heme unit is converted to bilirubin
. Bilirubin is insoluble in plasma and attached to plasma proteins for transport
- unconjugated
. Removed from the blood by the liver and conjugated with glucuronide to render it water soluble
- conjugated
. Jaundice

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8
Q

Laboratory Tests for Red Blood Cells # 1

A

. Red blood Cell count ( RBC)
-Measures the total number of red blood cells in 1 mm 3 of blood
. Percentage of reticulocytes ( normally approximately 1%)
-Provide an index of the rate of red cell production

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9
Q

Laboratory Test for Red Blood Cells # 2

A

. Hemoglobin ( grams per 100 mL of blood)
- Measures the hemoglobin content of the blood
. Hematocrit
- Measures the volume of red cell mass in 100 mL of plasma volume

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10
Q

Transfusion Therapy

A

. Provides the means for replacement of red blood cells and other blood components
. Four major ABO blood types are determined by the presence or absence of two red cells antigens : A and B
- The presence of D antigen determines the Rh- positive type
- The absence of the D antigen determines the eh negative type

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11
Q

Red blood cell components used in transfusion therapy

A
. Whole blood 
.Red blood cells
. Leukocytes reduced blood cells
. Washed red blood cells
 . Frozen red blood cells
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12
Q

Signs and symptoms of transfusion Reactiond

A

. Sensation of heat along the vein where the blood is being infused
. Flushing of the face
. Urticaria, headache, pain in the lumbar area
. Chills, fever, constricting pain in the chest
. Cramping pain in the abdomen
. Nausea, vomiting
. Tachycardia, hypotension, and dyspnea

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13
Q

Anemia

A

. Definition
- An abnormally, low number of circulating red blood cells or level of hemoglobin, or both
- Results is diminished oxygen- carrying capacity
. Causes
- Excessive loss or destruction of red blood cells
- Deficient red blood cell production because of a lack of nutritional elements or bone marrow failure

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14
Q

Manifestations of Anemia

A

. Impaired oxygen transport with resulting compensatory mechanisms
. Reduction in red cell indices and hemoglobin levels
. Signs and symptoms associated with the pathological process that is causing the anemia

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15
Q

Anemias of deficient red cell production

A
. Iron deficiency anemia
. Megaloblastic anemia
- Cobalamin deficiency anemia
- Folic acid deficiency anemia
. Aplastic anemia
. Chronic disease anemia
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16
Q

G6PD

A

. A hereditary deficiency of glucose -6 phosphate dehydrogenase predispose to oxidative denaturation of hemoglobin, with resultant red cell injury and lysis

17
Q

Intravascular and extracvascular hemolysis

A

. Extra vascular hemolysis occurs when red blood cells become less deformable, making it difficult for them to transverse the splenic sinusoids

. Intravascular hemolysis occurs as a results of complement fixation in transfusion reactions, mechanical injury, or toxic factors.

18
Q

Sickle Cell Disease and Thalassemias

A

. Sickle cell disease is an inherited disorder in which an abnormal hemoglobin leads to chronic hemolytic anemia, pain, and organ failure
. The thalassemias are a group of inherited disorders of hemoglobin synthesis leading to decreased synthesis of either the a- or b globin chains of HbA

19
Q

Cause of sickling in sickle cell disease

A

. The abnormal structure of Hbs results from a point mutation in the b chain of the hemoglobin molecule, with an abnormal substitution of a single amino acid, valine, for glutamic acid

20
Q

Iron deficiency Anemia

A

. Iron deficiency is a common worldwide cause of anemia affecting people of all ages. The anemia results from dietary deficiency, loss of iron through bleeding, or increased demands.
. Because iron is a component of heme, a deficiency leads to decreased hemoglobin synthesis and consequent impairment of oxygen delivery.

21
Q

Vitamin B12 Deficiency

A

. The hallmark of vitamin B12 deficiency is megaloblastic anemia
. When vitamin B12 is deficient, the red cells that are produced are abnormally large because of excess cytoplasmic growth and structural proteins.

22
Q

Causes of Aplastic Anemia

A

. Among the causes of aplastic anemia are exposure to high doses of radiation, chemicals, and toxins that suppress hematopoiesis directly or through immune mechanisms

23
Q

Polycythemia # 1

A

. Definition
- A condition in which the red blood cell mass is increased

. Types
- Relative polycythemia: : results from a loss of vascular fluid and is corrected by replacing the fluid

24
Q

Polycythemia # 2

A
  • Primary polycythemia: a proliferative disease of the bone marrow with an absolute increase in total red blood cell mass accompanied by elevated white cell and platelet counts
  • Secondary polycythemia: results from increased erythropoietin levels caused by hypoxia conditions such as chronic heart and lung disease
25
Q

Polycythemia Manifestations

A

. Variable and related to an increase in RBC’s , hemoglobin level, and hematocrit with increased blood volume and viscosity

  • Splenomegaly
  • Depletion of iron
  • Disrupted cardiac output
  • hypertension
  • Decreased cerebral blood flow
  • Venous stasis
  • Thromboembolism and hemorrhage
26
Q

Neonatal Blood

A
. Hemoglobin Concerntrations at birth are high, reflecting the high synthetic activity in utero to provide adequate oxygen delivery.
- HbF versus HbA
. Affinity of F versus A
. Hyperbulirubinemia
- unconjugated versus conjugated 
- Phototherapy 
. Hemolytic disease
27
Q

Aging and Red Blood Cells # 1

A

. Age - associated decline in the hematopoietic reserve

  • Reduction in hematopoietic progenitors
  • Reduced production of hemotopoietic growth factors
  • Inhibition of erythropoietin
  • Inflammatory cytokines interfere with erythropoietin interaction with its receptors.
28
Q

Aging and Red Blood cells# 2

A

. Anemia
- Hb decreases with age
- RBC production decreases with age
- Complete blood count
. Peripheral blood smear and a reticulocyte count and index
- Studies to rule out comorbid conditions such as malignancy, gastrointestinal conditions that cause bleeding , pernicious anemia