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Anemia

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Diagnostics: bone marrow exam. Aplastic anemia. Interventions: Removal of causative agent ... Bone marrow transplant. Assignment ... – PowerPoint PPT presentation

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Title: Anemia


1
Anemia
  • Presented by
  • Manny Ramos RN, MSN

2
Crossmatching game for RBC laboratory test values
  • Reticulocytes
  • Hematocrit
  • MCV
  • MCHC
  • MCH
  • Crossmatch items from this column that correspond
    correctly to the definitions in the other column
  • Ave. volume of individual RBCs
  • Number of immature RBCs/mm3 blood
  • of circulating RBCs/mm3 blood
  • calculated ave. weight of Hg/RBC
  • Ave. concentration or of Hg/RBC
  • Packed vol. of RBCs in 100ml blood

3
Pathophysiology
  • Decreased RBC production
  • Iron deficiency
  • Folic acid deficiency
  • Aplastic anemia
  • Increased RBC loss or destruction
  • sickle cell anemia
  • blood loss
  • infection


4
Iron deficiency anemia
  • Causes
  • inadequate dietary iron intake
  • Malabsorption gastrectomy, chronic diarrhea,
    celiac sprue
  • increased iron needs pregnancy and lactation
  • chronic occult blood loss bleeding ulcers, GI
    inflammation, hemorrhoids, cancer, chronic
    hemoglobinuria
  • Menstrual blood loss

5
Iron Deficiency anemia
  • Diagnostics
  • Iron levels
  • Total iron-binding capacity (TIBC)
  • Serum Ferritin
  • Medications
  • Iron supplements, oral or parenteral
  • Vit. C

6
Vit. B12 deficiency anemia
  • Causes
  • Pernicious anemia lack of intrinsic factor
  • ileal resections, loss of pancreatic secretions,
    chronic gastritis
  • Strict vegetarians
  • Diagnostics
  • Schilling test
  • Medications
  • Vit. B12 parenteral

7
Folic acid deficiency anemia
  • Inadequate intake
  • Chronically malnourished
  • Older adults
  • Alcoholics
  • Drug addicted persons
  • Increased need
  • Pregnant women neural tube defects in fetus
  • Persons experiencing rapid growth
  • Malabsorption disorders Celiac sprue
  • Persons taking methotrexate and other
    chemotherapy

8
Sickle cell anemia
  • Pathophysiology
  • Autosomal recessive genetic defect
  • Hypoxemia abnormal HbS deoxygenated
  • crescent or sickle shape RBC
  • Sickled cells clump together
  • weakened RBCs, hemolyzed
  • shortened RBC life span

9
Sickle cell anemia
  • Sickle cell crises arise from
  • Hypoxia
  • Low environmental or body temperature
  • Excessive exercise
  • Anesthesia
  • Dehydration
  • Infection
  • Acidosis

10
Sickle cell crises
  • Manifestations
  • pallor, fatigue, jaundice, irritability
  • Painful swelling hands and feet, large joints,
    priapism, abdominal pain, stroke
  • Aplastic anemia
  • Blood pools in liver and spleen
  • Diagnostics Sickle cell test

11
Interventions
  • Hydration
  • Oxygen
  • Rest
  • Pain management
  • Treat precipitating factors
  • Folic acid supplementation
  • Blood transfusions
  • Genetic counseling

12
Thalassemia
  • Inherited disorder of hemoglobin synthesis
  • alpha or beta chains of hemoglobin are missing
    or defective
  • Manifestations
  • Minor asymptomatic mild anemia, splenomegaly,
    bronze skin, bone marrow hyperplasia
  • Major severe anemia, heart failure, liver and
    spleen enlargement fractures of long bones,
    ribs, vertebrae
  • Diagnostics Hemoglobin electrophoresis

13
Acquired hemolytic anemia
  • Causes
  • Mechanical trauma to RBC prosthetic heart valves
  • Autoimmune disorders
  • Bacterial or protozoan infection
  • Immune system-mediated responses
  • drugs, toxins, chemical agents, venoms
  • Manifestations
  • Anemia
  • splenomegaly, jaundice, pathologic fractures

14
Glucose -6-Phosphate Dehydrogenase (G6PD) Anemia
  • Hereditary defect in RBC metabolism
  • Direct oxidation of hemoglobin damages RBC
  • occurs when person exposed to stressors aspirin,
    sulfonamides, Vitamin K derivatives
  • Manifestations pallor, jaundice, hemoglobinuria,
    elevated reticulocyte count
  • Diagnostics quantitative assay of G6PD

15
Aplastic anemia
  • Bone marrow failure decreased RBC, WBC,
    platelets
  • Marrow replaced with fat
  • Causes idiopathic
  • Viral infections
  • stem cell damage from radiation
  • Exposure to chemicals
  • Certain antibiotics (chloramphenicol)
  • Chemotherapeutic drugs

16
Aplastic anemia
  • Manifestations vary with onset and severity of
    pancytopenia
  • Pallor, fatigue, headache, exertional dyspnea,
    tachycardia, heart failure
  • Bleeding due to low platelet levels
  • Fever, increased infection risk due to
    low WBC
  • Diagnostics bone marrow exam

17
Aplastic anemia
  • Interventions
  • Removal of causative agent
  • Blood transfusions
  • Bone marrow transplant

18
Assignment
  • Identify 3 priority nursing diagnoses for anemia
    and formulate nursing care plan for anemia
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