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Sickle cell anemia, Iron deficiency, Immune thrombocytopenia, Henoch…
Sickle cell anemia
Treatment
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Prevent infections: Vaccinations – pneumococcal, h. flu, meningiococcal & PVK
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Pathophysiology
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- Increased RBC destruction
Abnormal adhesion/entanglement/enmeshing + inflammatory response = intermittent blockage of microcirculation -> Vaso occlusion
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- obstruction caused by sickled RBCs
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Clinical manifestations
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Sequestration crisis
Pooling of large amounts of blood (hepatomegaly, splenomegaly, circulatory collapse)
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HgbA is replaced by Hgb S
Autosomal recessive disorder
One of the most common genetic diseases worldwide (incidence vary geographically)
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Sickle cell Disease
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Symptomatic, prone to Sickle Cell Crisis
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Iron deficiency
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Prevention
Nutritional findings
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Fe rich foods (rice cereal after 4-6 mo) (white food is bad aka milk) ( vitamin C helps body use Fe from food)
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Nursing
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Educate
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Side effects of iron supplements (constipation, teeth staining, etc.)
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What is it
Condition occurring when the body stores of iron drop too low to support normal red blood cell (RBC) production.
Immune thrombocytopenia
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Other facts
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Most are less than 10 years old, peak incidence 1-6 years
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Treatment
Anti-D antibody is plasma derived immunoglobulin that causes a transient hemolytic anemia in RhD positive patients with ITP
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Hemophilia
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Diagnosis
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History, labs, & exam
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Normal - PT, fibrinogen & platelets
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History of bleeding episodes (circumcisions, injections, etc.)
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Pathophysiology
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Hemarthrosis
bleeding in joint cavities (knees, elbows, ankles)
Early signs: stiffness, tingling, or ache
Obvious/late signs: warmth, redness, severe pain, loss of movemen
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