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clinical manifestations, medical management for each type of anemia
anemia
low hemoglobin (male: 14-18, female: 12-16)
avoid use of body extremity
pallor (paleness of skin)
fatigue
irritability
sickle cell anemia
chronic pain
sickle cell crisis (pain in hands/feet/arms/torso/legs)
pain is stabbing, squeezing, pins and needles
aplastic anemia
failure of bone marrow to produce rbcs, underproduction
inherited, acquired then not diagnosed until adulthood
hemolytic anemia
infraction/ischemia of body tissue
vitamin deficiency anemia
low vitamin B12 and folate levels
“bounding” feelings of a heartbeat
pernicious anemia
autoimmune destruction of gastric parietal cells, leading to a lack of intrinsic factor needed to absorb vitamin B12
treatment of anemias
sickle cell anemia
management of pain crises → narcotic pain medication, patient coltrolled analgesia, warm compress
iv fluids
blood tranfusion
prophylactic antibiotics (reduce the risk of infection)
aplastic anemia
blood transfusion
medications for infection
bone marrow transplant
vitamin deficiency anemia
iron supplement (ferrous sulfate)
anemia as symptom vs. primary disease
symptom
manifestation of another underlying condition
hematocrit and hemoglobin levels are a clue, not the root
treat the cause
can be inherited or sudden
primary
not caused by another condition
management of disease itself
can be inherited or sudden
often chronic or genetic
different categories and specific types of anemia
sickle cell anemia
aplastic anemia
hemolytic anemia
vitamin deficiency anemia
pernicious anemia